From owner-biophysics@net.bio.net Wed Oct 01 23:00:00 1997
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Date: Wed, 01 Oct 1997 20:22:39 -0600
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Subject: Re: UNIQUE METHOD OF TREATMENT !!!
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In article ,
  David Scott  wrote:
>
> bollocks is the phrase that springs instantly to mind......


 I have the results of serious scientific experiments
 and a concrete results of treatment of people !!!

 But your have only your crappy newspaperese...


 Without the best regards,
 Valery Kotul.

-------------------==== Posted via Deja News ====-----------------------
      http://www.dejanews.com/     Search, Read, Post to Usenet

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From: baskin@BIOSCI.MBP.MISSOURI.EDU (Tobias Baskin)
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Subject: Re: UNIQUE METHOD OF TREATMENT !!!
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Greetings,
	Valery Kotul wrote,

>
> I have the results of serious scientific experiments
> and a concrete results of treatment of people !!!

	Sorry Valery, but placebos work 40% of the time. Fact is, some
folks will recover if you give em scrabled eggs, served up with the right
kind of sauce.

	Tobias Baskin



From owner-biophysics@net.bio.net Wed Oct 01 23:00:00 1997
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From: Toke Lindegaard Knudsen <tlk@math.ku.dk>
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Subject: Breaking the barriers between biology, chemistry and physics.
Date: Thu, 2 Oct 1997 15:25:32 +0200
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I am submitting this very interesting article on behalf of Madhavendra
Puri of the Bhaktivedanta Institute.  Could anyone replying to this
posting on the newsgroup please CC a copy to Madhavendra Puri at
<tumle@diku.dk>.  That would be most helpful for me.  Thank you!
-Toke Lindegaard Knudsen.


          EVIDENCE THAT ATOMS BEHAVE DIFFERENTLY IN
           BIOLOGICAL SYSTEMS THAN OUTSIDE OF THEM

                    Madhavendra Puri 
              The Bhaktivedanta Institute
                 E-mail: tumle@diku.dk

   A number of chemists report that plants, animals and human beings
ROUTINELY TRANSMUTE MID-RANGE ELEMENTS (for example, potassium into 
calcium or magnesium into calcium) AS PART OF THEIR ORDINARY DAILY 
METABOLISM. These transmutations obey rules such as:  Mg + O => Ca;  K + H 
=> Ca. This is revolutionary since, according to current physical theory, 
the energy levels required for such transmutations are billions of times
higher than what is available in biological systems. Equally inexplicable
fission reactions such as Ca => Mg + O; Ca => K + H are also reported.
But revolutions in physics have repeatedly occurred, such as the quantum
revolution in which the radical property of non-locality, previously
considered impossible, is now accepted by physicists  (see Aspect and
Grangier 1986, Bransden and Joachain 1989, p.671-681, Chiao et al 1993,
Squires 1990, p.173, Rae 1986, p.25-44, and Penrose 1990, p.369).   
   What I am presenting here is not the "cold fusion" of Fleischmann and
Pons which, as far as I know, lacks clear evidence of actual fusion. Even
if the Fleischmann and Pons effect turns out to be actual fusion, it is
only the fusion of isotopes of the lightest element hydrogen under special 
laboratory conditions which is quite different from the UNEQUIVOCAL FUSION 
AND FISSION OF MID-RANGE elements found in biological transmutation reports.
 
   Now let us examine the evidence for biological transmutation. Crabs,  
shellfish and crayfish have shells made largely of calcium. A crab 17 cm
by 10 cm has a shell weighing around 350 grams. Periodically these animals  
shed their shell and create a new one. This is called molting. When
molting, a crab is very vulnerable and hides away from all other creatures
so it can not get calcium by preying on other creatures. According to
French chemist C. Louis Kervran of the Conseil d'Hygiene in Paris, sea
water contains far too little calcium to account for the rapid production
of a shell (the calcium content of sea water is about 0.042% and a crab
can form a new shell in little more than one day). If the entire body of a  
crab is analyzed for calcium, it is found to contain only enough calcium
to produce 3% of the shell (even taking into account the calcium carbonate
stored in the hepato-pancreas just before molting).
   Even in water completely devoid of calcium, shellfish can still create
their calcium-bearing shells as shown by an experiment performed at the
Maritime Laboratory of Roscoff: "A crayfish was put in a sea water basin
from which calcium carbonate had been removed by precipitation; the animal  
made its shell anyway." (Kervran 1972, p.58)
   "Chemical analysis made on animals secreting their shells has revealed
that calcium carbonate is formed on the outer side of a membrane although
on the opposite side of the membrane, where matter enters, there is no
calcium. This fact has left specialists perplexed." (Kervran 1972, p.58) 
   Sea water contains a sufficient amount of magnesium to form a shell if
we accept Kervran's proposition that crabs routinely transmute magnesium
into calcium; Mg + O => Ca.
   It would be interesting to put a crayfish in water devoid of both
calcium and magnesium and see if it can still create its shell.

   Normal egg shells produced by hens contain calcium. Kervran (1972,
p.41) reported an experiment in which hens were confined in an area in
which there was no source of calcium and no calcium was present in their
diet. The calcium deficiency became clearly manifested after a few days
when the hens began to lay eggs with soft shells. Then purified mica
(which contains potassium) was given to the hens. Kervran (1972, p.41)
described what then transpired: "The hens jumped on the mica and began  
scratching around it very rapidly, panting over it; then they rested,
rolling their heads on it, threw it into the air, and began scratching it 
again. The next day eggs with normal shells (weight 7 grams) were laid.  
Thus, in the 20 hours that intervened, the hens transformed a supply of 
potassium into calcium. ... An experiment of this kind, using the same
mica, was undertaken with guinea-fowls over a period of forty days. The 
administering of the mica was suspended three times and each time a
soft-shelled egg was laid ... ."
   One might suggest that the calcium in the egg shells was borrowed from
the bones of the hens. But if this is true, why were soft eggs laid when
the mica was withheld and normal eggs laid when mica was given to the
hens? In order to avoid the conclusion that the hens transmuted potassium
into calcium, one would have to show that mica somehow stimulates a
metabolic pathway in which calcium is removed from the hen's bones and
used in the production of the egg shells. This could be completely refuted
by feeding the hens mica (and of course absolutely no calcium) for such a
long period of time that all the calcium in their bones would have been
completely exhausted. If after that time the hens still produce
calcium-bearing egg shells, we must conclude that the calcium in the egg
shells is not being taken from the bones. At that point, we seem to have
no choice but to acknowledge the transmutation of potassium into calcium
within the hens.
 
   Kervran (1972, p.52) described experiments performed in 1959 by the
French government in the Sahara desert. The government was interested in
determining the nutritional requirements of petroleum workers in the
extreme heat prevalent in the desert. In the first experiment, conducted
near a place called Ouargla, the total amount of magnesium ingested per
day per man was measured and compared with the amount excreted. It was
found that, on the average, each man daily excreted 117.2 milligrams of
magnesium more than he ingested. Thus, each day, each man lost on the
average 117.2 milligrams of magnesium. Now we must consider how much
magnesium is on reserve in the human body: it turns out that the body is
not able to mobilize more than 5000 milligrams of magnesium. Thus, at a
daily loss of 117.2 milligrams, it is clear that after 50 days the bodies
of the petroleum workers should have been completely depleted of
magnesium. But the experiment was conducted for 180 days and each day each
man excreted on the a verage 117.2 milligrams more than he ingested.
   The second experiment lasted for 240 days and was conducted near
Tindouf which has a drier climate. This time each man excreted each day an
average of 256 milligrams of magnesium more than he ingested. Under these
conditions, after 20 days, each man should have been completely depleted
of magnesium; but somehow they survived for 220 days thereafter. It seems
difficult to avoid the conclusion that the human body is able to create
magnesium.

   Biochemist H. Komaki of the University of Mukogawa in Japan reported
that a number of different families of microorganisms such as Aspergillus
niger and Saccharomyces cerevisiae create potassium during growth. (Komaki
1965, 1967)

   Kervran described a germination experiment using ryegrass seeds (type
Rina) performed in 1971 by the Laboratory of the Societe des Agriculteurs
de France (Kervran 1972, p.107). Out of an initial group of 2000 seeds,
1000 were set aside as a control batch and the other 1000 were germinated.
The control batch weighed 2.307 grams before drying and 2.035 grams after
drying. These 2.035 grams were analyzed and found to contain 3.02
milligrams of magnesium, 6.97 milligrams of potassium, 6.00 milligrams of
calcium and 0.021 milligrams of copper. The magnesium, calcium and copper
contents were determined by atomic absorption spectroscopy and the
potassium content was determined by flame emission.
   The 1000 seeds to be germinated were germinated for 29 days in Petri
dishes under a plastic sheet to insure that no dust could get in. Aside
from 430 milliliters of Evian water, absolutely nothing else was supplied
to the seeds during germination. 430 milliliters of Evian water was found
to contain 10.32 milligrams of magnesium, 0.39 milligrams of potassium,
33.11 milligrams of calcium and 0.00 milligrams of copper.
   After the 29 day germination period, the plants were converted to ashes
under high temperature and the ashes and residual Evian water in the Petri
dishes were found to contain 3.20 milligrams of magnesium, 16.67
milligrams of potassium, 36.50 milligrams of calcium and 0.10 milligrams
of copper.
   Before germination there were 6.97 milligrams of potassium in the
seeds. During germination 0.39 milligrams of potassium were added to the
growing plants (this came from the Evian water). If atomic nuclei can not
be altered in biological systems, we expect that after germination there
should be 6.97 + 0.39 = 7.36 milligrams of potassium in the plants and
residual Evian water. But this was not the case. After germination the
plants and residual Evian water were found to contain 16.67 milligrams of 
potassium. Thus 9.31 milligrams of potassium were apparently created
during germination. 
   Before germination there were 3.02 milligrams of magnesium in the
seeds. During germination 10.32 milligrams of magnesium were added to the
growing plants (this came from the Evian water). If atomic nuclei can not
be altered in biological systems, we expect that after germination there
should be 10.32 + 3.02 = 13.34 milligrams of magnesium in the plants and
residual Evian water. But after germination the plants and residual Evian 
water were found to contain only 3.20 milligrams of magnesium. Thus 10.14  
milligrams of magnesium were apparently destroyed during germination. 
   Before germination there were 0.021 milligrams of copper in the seeds. 
During germination 0.00 milligrams of copper were added to the growing
plants. Assuming that atomic nuclei can not be altered, we expect that
after germination there should still be 0.021 milligrams of copper in the
plants and residual Evian water. But it turned out that after germination
the plants and residual Evian water were found to contain 0.10 milligrams
of copper. Thus 0.079 milligrams of copper were apparently created during  
germination. 
   Before germination there were 6.00 milligrams of calcium in the seeds.  
During germination 33.11 milligrams of calcium were added to the growing 
plants (from the Evian water). Assuming that nuclei can not be altered, we  
expect that after germination there should be 39.11 milligrams of calcium
in the plants and residual Evian water. However, after germination the
plants and residual Evian water were found to contain 36.50 milligrams of  
calcium. Thus 2.61 milligrams of calcium were apparently destroyed during 
germination.
   The following challenge can be made: no one knows how much potassium,
calcium, magnesium and copper was in the seeds before they were
germinated. It was assumed that the amounts of these elements was not
significantly different from the amounts of these elements in the control 
batch. How do we know this is true? What should have been done is to start 
with a 100 grams of seeds, mix them around thoroughly, weigh out 50
batches of 2.000 grams each, randomly select 25 of these as control
batches, determine the amounts of potassium, calcium, magnesium and copper
in these batches and note the maximum variation in these elements among
these batches. The remaining 25 batches can then be germinated and the
plants analyzed for element content. In this way we would have some
measure of the variation among different batches (both germinated and  
control). 
   On the positive side, it can be argued that since the seeds of the
control and germinated batches were of the same type, the variation in
element content between these two batches was not significant. Some
support for this idea can be found in the data provided by chemist D. Long
of the Michaelis Nutritional Research Laboratory in Harpenden, England.  
Long analyzed (using atomic spectroscopy) six batches of ryegrass seeds
(each of which weighed 5.4 grams before drying) and discovered that the  
difference in potassium content between the batch containing the greatest
amount of potassium and the batch containing the least amount of potassium  
was 0.054 milligrams of potassium per gram of dry seed weight. Similarly,  
the maximum difference in magnesium content was 0.033 milligrams per gram
of dry seed weight, that of calcium was 0.091 milligrams per gram of dry
seed weight, and that of copper was 1.19 micrograms per gram of dry seed 
weight. (Long 1971, p.7) 
    Kervran proposed that the plants performed the following nuclear  
reactions: Mg + O => Ca; Ca => K + H. Kervran did not discuss the reaction 
involving copper.
    Based on experience derived from similar experiments, Kervran said
that if the seeds are germinated in doubly-distilled water, the amount of 
transmuted material is much smaller and may fall within the range of 
experimental error and therefore not be significant. The reason for this
is that each kind of plant is only able to transmute certain elements into 
certain other elements. Thus the experimenter must provide the plant with
a certain amount of certain elements if he wants to observe a large amount 
of transmuted material. For germinating ryegrass seeds, Evian water is the 
perfect growth medium because it provides this particular kind of plant
with the elements it needs.
   Kervran (1972, p.132) also described a series of experiments in which 
wheat and oat seeds were germinated "on porous ashless paper saturated
with a fertilizing solution of salts dissolved in water. The solution was 
free of calcium." In the case of wheat (Roux Clair) there was 3.34 times
more calcium in the plants than in the seeds; in the case of one kind of 
oats (Noire du Prieure) there was 4.16 times more calcium in the plants
than in the seeds; in the case of another kind of oats (Panache de Roye)
there was 4.51 times more calcium in the plants than in the seeds. The 
calcium content was determined by two independent methods (conventional 
chemical analysis and atomic absorption spectroscopy); both methods agreed 
closely. Kervran performed more than 20 such experiments, mostly on oat 
seeds.
   Kervran (1972, p.133) mentioned that the moon plays an important role
in the production of calcium. The above huge increases in calcium were 
obtained in experiments in which the germination started at the new moon 
and stopped on the second full moon (after 6 weeks). This is an important 
consideration for those who attempt to duplicate these results. A lunar 
influence on the metabolic activity of various plants and animals was also 
reported by biologist Frank A. Brown. (Gauquelin 1969, p.131-133) 
   D. Long questioned Kervran's methods of analysis. Long (1971, p.9) said 
that Kervran had made (in some of his earlier experiments) the mistake of 
comparing the ash weight of the control batch with the ash weight of the 
plants after germination. Kervran may have made this mistake in some of
his earlier experiments but he did not do so in the ryegrass, wheat and 
oat germination experiments described above. In these experiments, he 
rightly compared the weight of the control batch with the weight of the 
seeds to be germinated. In other words, the weight comparison was done on 
the two batches of seeds before one batch was germinated. This is the 
correct procedure as acknowledged by Long himself.
   Long germinated ryegrass seeds in deionized water and reported that he 
was unable to observe a transmutation of elements. As discussed above,
this is to be expected since without a sufficient input of certain
elements, there is insufficient material to be transmuted. 
   A more serious criticism is Long's claim that he corresponded with 
Kervran who advised him to germinate green lentil seeds (Leguminacae) in 
water containing certain minerals. Long reported that although he did this 
he was still unable to observe a significant transmutation of elements. 
But Long did not attempt to duplicate the best of Kervran's germination 
experiments, namely the ryegrass, wheat and oat experiments described 
above. I hope that many scientists will do these experiments and report
the results to the scientific community.
   In the 1950s Pierre Baranger, a professor and the director of the 
Laboratory of Organic Chemistry at the Ecole Polytechnique in Paris, 
performed a large number of germination experiments and concluded that 
plants routinely transmute elements. Baranger did his experiments 
independently of Kervran. Baranger said: "My results seem impossible, but 
here they are. I took every precaution. I repeated the experiments many 
times. I made thousands of analyses for years. I had the results verified 
by third parties who did not know what I was investigating. I used several 
methods. I changed my experimenters. But there is no escape. We must
submit to the evidence: plants transmute elements." (Michel 1959, p.82) 
   I tried to get more information by writing letters to the Ecole 
Polytechnique, the Societe des Agriculteurs de France and the Agronomie 
Research National Institute, but I received no reply.
 
   In 1975 chemists O. Heroux and D. Peter of the Division of Biological 
Sciences of the National Research Council of Canada conducted a meticulous 
experiment with rats (Heroux and Peter 1975). They measured the amount of 
magnesium ingested through food, water (and even air) as well as the
amount of magnesium excreted in the form of urine and feces over three 
periods of time: 69 days, 240 days and 517 days. In the case in which the 
rats were fed a diet in which the amount of magnesium ingested was less
than the amount of magnesium excreted, it was expected that the total 
amount of magnesium in the body would decrease. In fact, long before the 
517th day of the experiment it was expected that there would be zero 
magnesium in the body. However, when the rats were analyzed for total 
magnesium on the 517th day, each rat contained, on the average, 82 
milligrams of magnesium. The method used to determine the amount of 
magnesium in the body, food, water, air, feces and urine was atomic 
absorption spectroscopy. 
   Heroux and Peter verified the accuracy of their determinations by 
giving samples to two other laboratories (the Division of Chemistry at the
National Research Council and the Department of Chemistry at McMaster 
University); both of these laboratories obtained essentially the same 
results as Heroux and Peter at the Division of Biology at the National 
Research Council. Finally, other methods were used (such as destructive 
neutron activation and spectrographic emission) and these methods yielded
results very similar to those obtained using atomic absorption 
spectroscopy. 
   I do not advise the replication of this experiment since it involved 
killing the rats in order to analyze their bodies for magnesium. 
Experiments involving animal killing are not required since there are many 
ways (as described above) to verify biological transmutation without such
killing. 

                        Bibliography

Albert, D. "Bohm's Alternative to Quantum Mechanics." 
Scientific American, May 1994, pages 32-39

Aspect, A. and Grangier, P.  "Experiments on Einstein-
Podolsky-Rosen-type Correlations with Pairs of Visible Photons."
In Quantum Concepts in Space and Time (edited by R. Penrose and 
C. J. Isham). Oxford: Oxford University Press, 1986

Bohm, D. and Peat, F. Science, Order and Creativity. 
New York: Bantam Books, 1987

Bransden, B. and Joachain, C. Introduction to Quantum Mechanics. 
Essex: Longman Group U.K. Limited, 1989

Chiao, R., Kwait, P. and Steinberg, A. "Faster than light?" 
Scientific American, August 1993, pages 38-46

Darnell, J., Lodish, H. and Baltimore, D. Molecular Cell Biology. 
New York: W. H. Freeman and Co., 1990

Gauquelin, M. The Cosmic Clocks. London: Peter Owen, 1969

Heroux, O. and Peter, D. "Failure of balance measurements to 
predict actual retention of magnesium and calcium by rats as 
determined by direct carcass analysis." Journal of Nutrition, 
1975, volume 105, pages 1157-1167

Kervran, C. Louis. Biological Transmutation. 
New York: Swan House Publishing Company, 1972

Komaki, H. "Sur la formation de sels de potassium par 
differentes familles de microorganismes dans un milieu sans 
potassium." Revue de Pathologie Comparee, Paris, September 1965

Komaki, H. "Production de proteines par 29 souches de 
microorganismes et augmentation du potassium en milieu de 
culture sodique, sans potassium." Revue de Pathologie Comparee, 
Paris, April 1967

Long, D. B. "Laboratory Report on Biological Transmutation." 
Monograph of the Henry Doubleday Research Society. 
Braintree, Essex, England, September 1971

Michel, A. "Un savant francais bouleverse la science atomique."
Science et Vie, Paris, 1959, pages 81-87

Penrose, R. The Emperor's New Mind. New York: Vintage Press, 1990

Rae, A. Quantum Physics: Illusion or Reality? Cambridge: 
Cambridge University Press, 1986

Squires, E. Conscious Mind in the Physical World.
Bristol: Adam Hilger, 1990


From owner-biophysics@net.bio.net Wed Oct 01 23:00:00 1997
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From: prismx@earthlink.net (Claire Haller)
Newsgroups: bionet.neuroscience,bionet.biophysics,bionet.cellbiol
Subject: SCIENCE-WEEK: This Week's Headlines (3 Oct 97)
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Xref: biosci bionet.neuroscience:20454 bionet.biophysics:3570 bionet.cellbiol:8173

Headlines in This Week's SCIENCE-WEEK (October 3, 1997)
[complete news reports free at http://members.aol.com/sciweek]

1. International Concern Over Smuggling of Chlorofluorocarbons
2. Most Distant Galaxy Observed at Redshift 4.92
3. Electrochemical Growth Method for Creating Electrical Contacts
4. Relating Bond Energy to Catalysis in Catalytic Antibodies
5. A Synthetic Oligomer That Mimics Protein Folding
6. Possible Explanation for Levorotatory Amino Acids in Biology
7. A Block Copolymer of Collagen and Elastin in Marine Mussels
8. X-Ray Crystallography Evidence for Some Key Enzyme Structures
9. Analysis of Procapsid Assembly in Bacteriophage Virus
10. High Resolution Structure of the Nucleosome Core Particle
11. A New Theory of Myocardial Oxygenation in Fishes and Reptiles
12. Evidence for Self-Organization of Cell Microtubules
13. Mechanism of Action of Tumor Suppressor Protein p53
14. An Analysis of Action Potential Dynamics at Neuron Terminals
15. Identification of Gene Responsible for Mediterranean Fever
16. The Prospects for Gene Therapy
17. A New Drug Against Influenza Virus Infection
18. Chromosome Mis-Segregation in Alzheimer's Disease
19. High Concentrations of Cancer Inhibitor in Broccoli Sprouts
20. A Counter-Argument Against Pessimism in Cancer Research

The Editors
SCIENCE-WEEK
A Free Weekly Digest of the News of Science
prismx@earthlink.net
http://members.aol.com/sciweek


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Subject: test
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asdf


From owner-biophysics@net.bio.net Thu Oct 02 23:00:00 1997
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From: efulton@dres.dnd.ca (Elaine Fulton)
Newsgroups: bionet.biophysics
Subject: electromagnetic rotation assay
Date: Fri, 3 Oct 1997 14:00:47 UNDEFINED
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Several years ago an article appeared in New Scientist (15 May 93) on an 
electrorotation assay developed by Scientific Generics (Cambridge) and the 
University of Wales for the detection of microorganisms.  The method used 
polystyrene beads coated with antibodies to captureand detect the target 
antigen at  a sensitivity a million times greater than conventional 
techniques. the scientists involved in the development were Adrian Parton of 
Scientific Generics and Ron Pethig and Julian Burt of University of Wales. 
Does anyone have any further information on this development, have contacts 
with these scientists, or could anyone put me in touch with someone who could 
provide further information?  Any and all information would be most 
appreciated.  Thanks.  Elaine

From owner-biophysics@net.bio.net Fri Oct 03 23:00:00 1997
Path: biosci!daresbury!not-for-mail
From: <RUMYM@BGEARN.ACAD.BG>
Newsgroups: bionet.biophysics
Subject: Madhavendra Puri's paper (Pentcho Valev)
Date: 4 Oct 1997 09:49:52 +0100
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   There is a strange tendency in all discussion groups to which I have
contributed to leave any real problem unsolved. True, sometimes the
problems are not clearly set; however, paradoxically, it is only in this
case that an author can expect some critical or ironical comment. As soon
as the author manages to clarify the issue, nobody seems to care anymore
about the solution.
   The problem in Madhavendra Puri's paper "Evidence that atoms behave
differently in biological systems..." is quite clearly set and deserves
attention. What is bothering however is that there is no "microscopic"
evidence - either theoretical or experimental. On one hand, a specific
physical/chemical mechanism is looked for; on the other, the balance
arguments are like those used in the beginning of the century when the
principles of plant mineral nutrition were established.
   Perhaps Madhavendra would be so kind as to elaborate on the idea -
how can we interprete these transmutations at the molecular level? Which
enzymes are supposedly involved? Or the mechanism is not enzymatic at all?

Pentcho Valev

From owner-biophysics@net.bio.net Fri Oct 03 23:00:00 1997
Path: biosci!MAIN.INFOTEL.BG!steli
From: steli@MAIN.INFOTEL.BG (Stelios Papaioanou)
Newsgroups: bionet.biophysics
Subject: rezeroing effect
Date: 4 Oct 1997 10:23:44 -0700
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Hi all,
I'd be grateful to you if someone could explain me what is the "rezeroing
effect".
I read about it in Guyton's textbook of Physiology and there is a comparison
between this and sleep.

Thank you very much in advanced

Stelios Papaioanou
student of Medicine =20
Stara Zagora - Bulgaria
e-mail:steli@main.infotel.bg
=D3=F4=DD=EB=E9=EF=F2
Stelios Papaioanou
e-mail:steli@main.infotel.bg


From owner-biophysics@net.bio.net Fri Oct 03 23:00:00 1997
Path: biosci!daresbury!not-for-mail
From: <RUMYM@BGEARN.ACAD.BG>
Newsgroups: bionet.biophysics
Subject: Experimental model of a possible bioenergetic cycle (Pentcho Valev)
Date: 4 Oct 1997 13:31:05 +0100
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Original-To: biophys@dl.ac.uk

I would like to call attention to the following equilibrium system:

                            low pH

membrane-permeable-to-H+ only // impermeable-membrane-----------------X---

                            high pH

The problem is: At the point X on the impermeable membrane, is there a
transmembrane electrical force opposing movement of H+ down the concentration
gradient or not? If there is not, an ATPsynthase placed at the point X could
perform a concentration-driven ATP synthesis. As the system is at equilibrium,
this would be a violation of the second law.
   An experimental model could consist in the following. 1. H+ is replaced
with K+. 2. Two microelectrodes reversible for K+ (made of K amalgam) are
placed on the two sides of the impermeable membrane, at the point X.
   If there is a current between the electrodes, this would mean that there
is no transmembrane potential difference. Note that the current is
accompanied by disappearance of K+ where the concentration is high and
equivalent appearance where the concentration is low, i.e. the electrical
work is fully analogous to the chemical work obtained as the pH gradient
drives ATP synthesis.
   The experiment can even be simpler - no need to use an impermeable
membane - the microelectrodes should simply be placed far enough from the
permeable one:

  A     10 mM KCl                 M                 1 mM KCl          B

where M is a membrane permeable only to K+  and A and B are distant points
where the microelectrodes must be placed.

   I still believe that the question "Can ATP be synthesized in a system at
equilibrium?" makes a lot of sense. I would be very happy to find people
interested in the answer.

Best regards,
Pentcho Valev

From owner-biophysics@net.bio.net Sat Oct 04 23:00:00 1997
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From: scobi001@tc.umn.edu (Ron Scobie)
Newsgroups: bionet.biophysics
Subject: EEGDevice
Date: Sat, 04 Oct 1997 22:25:33 -1000
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I am trying to find an EEG like device that a high school student might
build or obtain(at low cost) for a science fair experiment.  Would any of
you be able to help?

-- 
scobie@anoka.k12.mn.us

From owner-biophysics@net.bio.net Sat Oct 04 23:00:00 1997
Path: biosci!agate!howland.erols.net!winter.news.erols.com!news
From: drake@erols.com
Newsgroups: bionet.biophysics
Subject: Equation for plant growth
Date: Sat, 04 Oct 1997 20:41:26 +0000
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Have the results of any research been used to formulate an 
equation for plant growth?  For example, the basic "water + CO2 + 
light energy = growth" formula; has there ever been a calculated ratio 
of CO2/light energy (x amount CO2/y amount of lumens, for example)?
     If such a ratio and equation do exist, have any been formulated 
that take into account temperature and nutrients?  For instance, in 
the above equation iron would play a role.
     Any help with finding this information would be greatly 
appreciated.  Thank you.

From owner-biophysics@net.bio.net Sat Oct 04 23:00:00 1997
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From: "Jonathan B. Marder" <marder@agri.huji.ac.il>
Newsgroups: bionet.biophysics
Subject: Re: Donnan potential - reply to Jonathan Marder (Pentcho Valev)
Date: Sun, 5 Oct 1997 12:33:14 +0200
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RUMYM@BGEARN.ACAD.BG wrote in message <617n52$aj@mserv1.dl.ac.uk>...
>... The infinity point has, by convention, a potential zero, so it
follows that the point
>near the right wall of the container has also a potential zero. If Ur
is
>the potential of the point far to the right and Uinf is the potential
of
>the reference infinity point, we have  Ur  -  Uinf  =  0, i.e. Ur = 0.
>
Pentcho, here is the crux of the problem. It is fine by me if you take
the "infinity point" as potential zero, but you can only do that for ONE
side of the membrane. Actually, in practice, since the space enclosed by
a membrane is finite, there is no infinity point inside a membrane
vesicle.

I hope that this helps.
Best regards, Jonathan


From owner-biophysics@net.bio.net Sat Oct 04 23:00:00 1997
Path: biosci!daresbury!not-for-mail
From: <RUMYM@BGEARN.ACAD.BG>
Newsgroups: bionet.biophysics
Subject: Donnan potential - reply to Jonathan Marder (Pentcho Valev)
Date: 5 Oct 1997 10:37:38 +0100
Lines: 65
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Jonathan Marder wrote:
RUMYM@BGEARN.ACAD.BG wrote in message <60tk8l$nk9@mserv1.dl.ac.uk>...  <

>    10 mM NaCl                 M                 1 mM NaCl            <
>                                                                       <
>where M is a membrane permeable only to Na+.                           <
>   All references say that the system is electroneutral everywhere     <
except                                                                  <
>close to the membrane. However the potential difference between any two<
>points in the two compartments is said to be about 60 mV. Measurements <
>seem to support this.                                                  <
The system is definitely *not* electroneutral. However, what happens far<
from the membrane is that electrical fields are small i.e. there are    <
virtually no potential differences WITHIN a compartment (except close to<
the membrane). The same goes for concentration.                         <

I agree.


>   Let us try to assess the electrical potential at a point far to the <
>right, near the right wall of the container. If a test positive charge <
is                                                                      <
>moved from infinity to this point, no electrical work will be done as  <
the                                                                     <
>point is neutral and no electrical field will be crossed.              <
Agreed|                                                                 <



>Therefore, the                                                         <
>potential at this point is zero.                                       <
NO - the potential *difference* is zero.                                <

You are right, but this is the potential difference between the distant
point far to the right and the reference point in infinity. The infinity
point has, by convention, a potential zero, so it follows that the point
near the right wall of the container has also a potential zero. If Ur is
the potential of the point far to the right and Uinf is the potential of
the reference infinity point, we have  Ur  -  Uinf  =  0, i.e. Ur = 0.

>The same holds true for a point far to                                 <
>the left, near the left wall of the container.                         <
Again, the potential *difference* is zero.                              <

Analogously, Ul = 0, where Ul is the electrical potential of a point far
to the left, near the left wall of the container.


>   Therefore, the potential difference between these two points distant<
>from the membrane is zero, what contradicts the thermodynamic          <
prediction                                                              <
>that the difference must be 60 mV.                                     <

>   This is the whole problem, and I would ask again electrochemists to<
>give their opinions. If the potential difference is indeed zero, the  <
>implications would be even difficult to imagine.                      <
It would pose a huge problem. However, s you see from my approach, the <
potential difference between two the points will be 60mV regardless of <
distance from the membrane.                                            <

I think I have shown that  Ur - Ul = 0, but maybe I do not see something.
Please correct me if I am wrong.

Best regards,
Pentcho

From owner-biophysics@net.bio.net Sat Oct 04 23:00:00 1997
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From: "Jonathan B. Marder" <marder@agri.huji.ac.il>
Newsgroups: bionet.biophysics
Subject: Re: Donnan potential (Pentcho Valev)
Date: Sun, 5 Oct 1997 09:36:44 +0200
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RUMYM@BGEARN.ACAD.BG wrote in message <60tk8l$nk9@mserv1.dl.ac.uk>...
>(Sorry if this message has appeared more than once - my e-mail system
>is down again)
>
>In reply to Jonathan Marder
>
>Jonathan, you deny the validity of both curves for equilibrium
conditions
>but do not suggest what the valid one should look like.

It's very simple really. if the system is *at equilibrium* (as you
stated), the electrochemical potential is (by definition) identical at
all points - plot this as a horizontal line. However,
this potential is the sum of concentration and electrical potential
which would look something like this where C=concentration, E=electrical
potential:-

--outside--|- membrane-|--inside--
EEEEEEEEEEE|(E)     (C)|CCCCCCCCCCC
           |  (E) (C)  |
           |    (X)    |
           |  (C) (E)  |
CCCCCCCCCCC|(C)     (E)|EEEEEEEEEEE

Inside the membrane things get complicated wince ACTUAL concentrations
are dependent on lipid solubility of the ion in question. Also, I have
ignored the localized perturbations near the membrane surface.

Actually we do not
>need to know the shape of the curve near the membrane; the essential
>problem is what happens to the electrical potential far from the
membrane.
>   Let me describe the system in concrete numbers:
>
>    10 mM NaCl                 M                 1 mM NaCl
>
>where M is a membrane permeable only to Na+.
>   All references say that the system is electroneutral everywhere
except
>close to the membrane. However the potential difference between any two
>points in the two compartments is said to be about 60 mV. Measurements
>seem to support this.
The system is definitely *not* electroneutral. However, what happens far
from the membrane is that electrical fields are small i.e. there are
virtually no potential differences WITHIN a compartment (except close to
the membrane). The same goes for concentration.


>   Let us try to assess the electrical potential at a point far to the
>right, near the right wall of the container. If a test positive charge
is
>moved from infinity to this point, no electrical work will be done as
the
>point is neutral and no electrical field will be crossed.
Agreed!

>Therefore, the
>potential at this point is zero.
NO - the potential *difference* is zero.

>The same holds true for a point far to
>the left, near the left wall of the container.
Again, the potential *difference* is zero.

>   Therefore, the potential difference between these two points distant
>from the membrane is zero, what contradicts the thermodynamic
prediction
>that the difference must be 60 mV.

>   This is the whole problem, and I would ask again electrochemists to
>give their opinions. If the potential difference is indeed zero, the
>implications would be even difficult to imagine.
It would pose a huge problem. However, s you see from my approach, the
potential difference between two the points will be 60mV regardless of
distance from the membrane.



From owner-biophysics@net.bio.net Sat Oct 04 23:00:00 1997
Path: biosci!daresbury!not-for-mail
From: <RUMYM@BGEARN.ACAD.BG>
Newsgroups: bionet.biophysics
Subject: Donnan potential (Pentcho Valev)
Date: 5 Oct 1997 12:51:18 +0100
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Jonathan Marder wrote:
Pentcho, here is the crux of the problem. It is fine by me if you take  <
the "infinity point" as potential zero, but you can only do that for ONE<
side of the membrane. Actually, in practice, since the space enclosed by<
a membrane is finite, there is no infinity point inside a membrane      <
vesicle.                                                                <

Yes here is the crux of the problem. But why should we change the system?
Let us solve first the problem for the case in which the right and left
side of the membrane have "equal rights", i.e. for the system

     10 mM KCl                   M                 1 mM KCl

where M is a membrane permeable only to K+.
   Do you agree that, at equilibrium, the potential difference between
points symmetrical with respect to but distant enough from the membrane
is zero? If yes, we will go immediately to the "vesicle" case - it is
more complicated but more interesting of course.

Pentcho

From owner-biophysics@net.bio.net Sat Oct 04 23:00:00 1997
Path: biosci!rutgers!uwm.edu!newsspool.doit.wisc.edu!news.itis.com!not-for-mail
From: Petr Kuzmic <pkuzmic@biokin.com>
Newsgroups: bionet.biophysics
Subject: Re: Madhavendra Puri's paper (Pentcho Valev)
Date: Sun, 05 Oct 1997 15:57:48 -0500
Organization: BioKin Consulting
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RUMYM@BGEARN.ACAD.BG wrote:
 
> an author can expect some critical or ironical comment.

Indeed.  Speaking of critical and ironical comments, I attach a copy of
a posting from sci.chem by a wickedly funny man named Uncle Al
Schwartz...

Petr Kuzmic (pkuzmic@biokin.com, http://www.biokin.com)

____________

Madhavendra Puri wrote:
> 
> I would like to request that anyone who replies to this article on the
> newsgroup kindly make a CC of the reply to me at tumle@diku.dk
> That will be a big help.  Thank you!
> -Madhavendra Puri.
> 
>           EVIDENCE THAT ATOMS BEHAVE DIFFERENTLY IN
>            BIOLOGICAL SYSTEMS THAN OUTSIDE OF THEM
> 
>                     Madhavendra Puri
>               The Bhaktivedanta Institute
>                  E-mail: tumle@diku.dk
> 
>    A number of chemists report that plants, animals and human beings
> ROUTINELY TRANSMUTE MID-RANGE ELEMENTS (for example, potassium into
> calcium or magnesium into calcium) AS PART OF THEIR ORDINARY DAILY
> METABOLISM. 

[SNIP]

SPACE ALIENS EAT DWARF MUTANT HEIRESS AND HER DOG!
RUN YOUR CAR ON WATER!
MIRACLE HORSE RACING COMPUTER!
BUNS OF STEEL!  ABS OF STEEL!  THINNER THIGHS IN 30 DAYS!
DEAD PSYCHICS HOTLINE!  WE KNEW YOU WOULD CALL!
QUARTZ CRYSTALS!  BEZOAR STONES!
5000 YOGIC FLOATERS TO CLEANSE THE EARTH OF ALL DISCORD!
SQUARE THE CIRCLE!  TRISECT THE ANGLE! LEARN THE MYSTERIES OF THE
ANCIENTS!
LAUNDRY RINGS CURE CANCER!
APPLE CIDER VINEGAR CURES CANCER!
MAGNETIC FIELDS CURE CANCER!
ELVIS MATERIALIZES AND CURES CANCER!
PRINCESS DI WAS SPACE ALIEN SENT TO EARTH TO CURE CANCER!

Dr. Schund and his Institute for Ethnoanthropoesy has joined forces with
Derrida Poswilly and the Institute for Institutional Analysis!  All
mathematics and science is at the verge of total obsolescence!  This is
the multi-level markieting extravaganza of the Millennium!  Act now to
lock in your territories for this fantastic and unstoppable overturn of
all human civilization!  Yada yada sis boom bah.

-- 
Uncle Al Schwartz
UncleAl0@ix.netcom.com ("zero" before @)
http://www.ultra.net.au/~wisby/uncleal.htm
 (Toxic URL! Unsafe for children, Democrats, and most mammals)
"Quis custodiet ipsos custodes?"  The Net!

From owner-biophysics@net.bio.net Sat Oct 04 23:00:00 1997
Path: biosci!BIOC.RICE.EDU!bartel
From: bartel@BIOC.RICE.EDU (Bonnie Bartel)
Newsgroups: bionet.biophysics
Subject: faculty positions-Rice University
Date: 5 Oct 1997 08:45:38 -0700
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Rice University
Department of Biochemistry & Cell Biology
Faculty Positions

  Applications are invited for two tenure-track faculty positions in
biological sciences, one in cell and developmental biology and one in
biophysics.  Cell and developmental biology may encompass animal,
microbial or plant systems, while biophysics areas include experimental,
computational and theoretical approaches.  Candidates must have
completed a Ph.D. or M.D./Ph.D. program in a related field, have
postdoctoral training, exhibit outstanding communication skills, and a
record indicating significant potential in research and teaching.  The
successful candidate will be expected to develop and maintain a vigorous
research program supported by extramural funding, and participate in
graduate and undergraduate teaching.  Emphasis in recruiting will be at
the Assistant Professor level, but highly qualified candidates at other
levels will also be considered.  Review of submitted applications will
commence on November 1, 1997, and continue until the positions are
filled.  Please send letter of application, curriculum vitae, summary of
past research, and statement of future research plans, and arrange for
four letters of reference to be sent to:
	Faculty Search Committee
	Department of Biochemistry & Cell Biology
	Rice University, MS-140
	6100 Main Street
	Houston, TX 77005-1892

Rice University is an Equal Opportunity/Affirmative Action Employer;
women and minority candidates are encouraged to apply.

From owner-biophysics@net.bio.net Sat Oct 04 23:00:00 1997
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From: "Jonathan B. Marder" <marder@agri.huji.ac.il>
Newsgroups: bionet.biophysics
Subject: Re: Donnan potential (Pentcho Valev)
Date: Sun, 5 Oct 1997 14:43:33 +0200
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RUMYM@BGEARN.ACAD.BG wrote in message <617uvm$57c@mserv1.dl.ac.uk>...
>Jonathan Marder wrote:
>Pentcho, here is the crux of the problem. It is fine by me if you take
<
>the "infinity point" as potential zero, but you can only do that for
ONE<
>side of the membrane. Actually, in practice, since the space enclosed
by<
>a membrane is finite, there is no infinity point inside a membrane
<
>vesicle.
<
>
>Yes here is the crux of the problem. But why should we change the
system?
>Let us solve first the problem for the case in which the right and left
>side of the membrane have "equal rights", i.e. for the system
>
>     10 mM KCl                   M                 1 mM KCl
>
>where M is a membrane permeable only to K+.
>   Do you agree that, at equilibrium, the potential difference between
>points symmetrical with respect to but distant enough from the membrane
>is zero?

No I do not!
The convention you mention of "points at infinity have zero potential"
cannot
be applied to both sides of the membrane - that would be quite wrong.
The purpose of the convention is to set a basline, not to ignore REAL
differences in potential. To maintain a tenfold concentration of K+ at
ANY separation (inc. infinity) requires a potential difference of 60mV.

Pentcho, this is a non starter for me. I still cannot accept that there
is any inherent contradiction in the accepted treatment of this topic.


From owner-biophysics@net.bio.net Sun Oct 05 23:00:00 1997
Path: biosci!bloom-beacon.mit.edu!senator-bedfellow.mit.edu!dtuch
From: dtuch@athena.mit.edu (David S Tuch)
Newsgroups: bionet.biophysics
Subject: extracellular conductivity
Date: 5 Oct 1997 15:45:00 GMT
Organization: Massachvsetts Institvte of Technology
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I've been scouring the lit for any values on the DC electrical conductivity of brain tissue extracellular space.  Any tips?  Thanks.

Dave Tuch
dtuch@nmr.mgh.harvard.edu   

From owner-biophysics@net.bio.net Sun Oct 05 23:00:00 1997
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From: "Dr E. Buxbaum" <EB15@le.ac.uk>
Newsgroups: bionet.biophysics
Subject: Re: EEGDevice
Date: Mon, 06 Oct 1997 09:46:06 -0700
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Ron Scobie wrote:
> 
> I am trying to find an EEG like device that a high school student might
> build or obtain(at low cost) for a science fair experiment. 

Building an amplifier for the bodies electrical signals (EEG, ECG and
EMG) is relatively straight forward. Get a book on electronics and look
under "instrumentation amplifier" to find the basic schematic. There are
good ic's now for this purpose, for example Burr-Browns INA 118. This
amplifier is usually followed by a low pass, to filter out mains hum,
and an output buffer with variable gain. Solder two large coins to the
inner core of screend cable and connect them to the inverting and
non-inverting  inputs of the amplifier. The screens of the cables are
connected to the common input, as is a third coin via unscreend cable
(the reference electrode). Smear the coins with a suitable conducting
gel (for example KY) and fix them to the body (head for eeg) of your
subject. 

The absolutely essential precondition is of course that all the circuits
are powerd by battery, NOT by mains. Otherwise you may electrocute your
subject! If you want to display the output of your amplifier on a PC
(probably the easies and cheapest way to do it, a suitable A/D converter
that connects to the printer port is in this months elector magazine),
you must use a laptop powered by batteries. Mains operated equipment is
definetly only for electronics engineers who know exactly what they are
doing.

There are realy nice experiments you can do with such a setup. Fix the
measuring electrodes to right hand and left foot, the reference
electrode to right foot and you get an ecg. Fix them across a muscle and
you'l get an emg. 

With a different sort of electrode you can also show regular electrical
signals in plants: Solder some silver wire to the cables as described
above. Electrolytically cover the wires with AgCl. Then poke them into
the plant (reference electrode goes into the soil). Try to do this with
plants which react on touch (like Mimosa pudica)! May be you can also
prove all those gardeners right who claim that plants grow better if you
talk to them.

The same setup can also be used to measure single nerve impulses in
insects, like gras hoppers. For this you have to take a freshly killed
insect and cut a window into the torax, to find the nerve which connects
the wing position sensor with the central nerve system (your teacher
should be able to help you with the anatomy, you'l also need a stereo
microscope for the operation). The nerve is then rested on the two
silver electrodes, the reference electrode is conneted to the insects
body and a metal screen around the setup. Remember to keep the nerve
moist with insect ringer. If you then carefully move around the wing,
you should be able to observe a change in the discharge frequency of the
nerve. The nerve has phasic-tonic characteristics, i.e. if you displace
the wing, the initial frequency of the discharge is proportional to the
degree of displacement, but after a while the frequency goes back to
normal. You'l have to work fairly quickly though, as the nerve will stop
to function some 2-3 h after the death of the insect.

From owner-biophysics@net.bio.net Sun Oct 05 23:00:00 1997
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From: <RUMYM@BGEARN.ACAD.BG>
Newsgroups: bionet.biophysics
Subject: Donnan potential (Pentcho Valev)
Date: 6 Oct 1997 13:39:33 +0100
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I asked:

>     10 mM KCl                   M                 1 mM KCl

>where M is a membrane permeable only to K+.                             <
>   Do you agree that, at equilibrium, the potential difference between  <
>points symmetrical with respect to but distant enough from the membrane <
>is zero?                                                                <

Jonathan Marder replied:
No I do not|                                                           <
The convention you mention of "points at infinity have zero potential" <
cannot                                                                 <
be applied to both sides of the membrane - that would be quite wrong.  <
The purpose of the convention is to set a basline, not to ignore REAL  <
differences in potential. To maintain a tenfold concentration of K+ at <
ANY separation (inc. infinity) requires a potential difference of 60mV.<
                                                                       <
Pentcho, this is a non starter for me. I still cannot accept that there<
is any inherent contradiction in the accepted treatment of this topic. <

Jonathan, the problem is not scientific - it is psychological. It is quite
normal that we reach different theoretical conclusions -in my opinion, the
comparison with the infinity reference point makes more sense; you believe
that the thermodynamic prediction is stronger. However it is not at all
normal that the experimental verification is so easy and yet nobody wants
to help. I am unlucky to live under conditions allowing no experimental
activity; so I have been trying for years to convince people to do the
experiment - one should only place two microelectrodes made of K amalgam
at the two ends of the container. If the measured voltage is zero,
thermodynamics is correct. If it is 60 mV, I would be right. (For this
type of electrodes thermodynamics predicts zero voltage).
   The experiment would cost a specialized lab not more than half an hour,
and the implications both thermodynamic and bioenergetic could be rather
important.
   What should I do? I am even ready to pay (although I am by no means the
reachest person in the world). Does anybody know what the proper behaviour
is in cases like this?

Best regards,
Pentcho

From owner-biophysics@net.bio.net Mon Oct 06 23:00:00 1997
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From: newaccounts@stopat.com
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Subject: Free FrontPage Web Site
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From owner-biophysics@net.bio.net Mon Oct 06 23:00:00 1997
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From: tivol@news.wadsworth.org (William Tivol)
Newsgroups: bionet.biophysics
Subject: Re: Donnan potential - how far from the membrane? (Pentcho Valev)
Date: 7 Oct 1997 21:29:02 GMT
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RUMYM@BGEARN.ACAD.BG wrote:

: (Bill, please, refer me to the book where you found the curve).

	P. R. Bergethon & E. R. Simons, Biophysical Chemistry: Molecules
		to Membranes.

I extrapolated from and combined some of the figures from the later chapters
of the book.  I took their figure for the potential where there was an ex-
cess of positive charge, inverted it for an excess of negative charge, and
combined them.  For the situation of the Na+-permeable membrane, the excess
of + is on the right (low [NaCl]) and - is on the left (high [NaCl]).
				Yours,
				Bill Tivol

From owner-biophysics@net.bio.net Mon Oct 06 23:00:00 1997
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From: John Philo <jphilo@amgen.com>
Newsgroups: bionet.biophysics
Subject: Re: extracellular conductivity
Date: Tue, 07 Oct 1997 13:09:47 -0700
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To: David S Tuch <dtuch@athena.mit.edu>

David S Tuch wrote:
> 
> I've been scouring the lit for any values on the DC electrical conductivity of brain tissue extracellular space.  Any tips?  Thanks.
> 
> Dave Tuch
> dtuch@nmr.mgh.harvard.edu

That value should be well known by the people who do
magnetoencephalography (i.e. the magnetic field equivalent to an EEG),
since that conductivity affects the signals they see.  Thus you may get
to what you are looking for by searching the MEG literature.  One name
to try would be John Wikswo (Vanderbilt), an old friend who I know did a
lot of theoretical work on propagation of EM waves through the brain as
well as experimental MEG studies.

Good luck,

John Philo, Protein Chemistry, Amgen

From owner-biophysics@net.bio.net Tue Oct 07 23:00:00 1997
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From: "Douglas B Kell" <dbk@aber.ac.uk>
Newsgroups: bionet.biophysics,bionet.cellbiol,bionet.metabolic-reg,bionet.microbiology
Subject: GRC Conference on Macromolecular Organisation and Cell Function 1998
Date: 7 Oct 1997 15:56:42 GMT
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Dear colleagues,

Together with my Co-Chair, Professor John Wilson of Michigan State
University, East Lansing, MI, USA, I would like to alert you to the
next Gordon Research Conference on "Macromolecular Organization and
Cell Function." The conference will be held at Oxford University, UK,
Sept. 13-18, 1998. A Gordon Conference with this theme has been held
in alternate years since 1987.

The focus of the conference is on the functional organization of
cellular components, and the critical role of this organization in
metabolism and its regulation. Initially, much of the attention was
directed at enzymes, but this has greatly expanded over the years to
include nucleic acids (e.g., targeting of mRNAs, assembly of
complexes associated with transcription or translation), membranes,
organelles, and delicate structures such as the nuclear matrix and
cytoskeleton. Principles governing the assembly of such structures,
as well as mechanisms by which these assemblies might be changed in
response to altered metabolic or hormonal status, or by
pharmaceutical intervention, are central issues in this conference. 

Conference participants have been especially sensitive to the fact
that much of this organization may be destroyed, or at least grossly
perturbed, when studies are performed in vitro. Thus, a persistent
feature in the conference has been the cautious extrapolation of in
vitro results to the in vivo condition, as well as development and
application of techniques that allow one to study cellular structure
and function in vivo. The result has been that this conference
traditionally brings together scientists with interests ranging from
biochemistry, cell biology, and molecular biology to theoretical
formalisms, quantitative modelling, biophysics, physics, and
(especially noninvasive) instrumentation. This truly
interdisciplinary nature has consistently led to broadly based
discussions and interactions which have been rated highly by those
in attendance.

We cordially invite you to participate in this next meeting.

Full details of the very exciting speaker list, and links to the
main GRC site (through whom applications to attend should be made),
can be found on the conference's Web site, which we would suggest 
that you might bookmark:

http://gepasi.dbs.aber.ac.uk/grc98.html

Although we hope to have targeted known parties likely to be
interested in participating, we be pleased if you could alert any of
your other colleagues whose interests overlap those of the 
Conference.

Kind regards and best wishes,
Douglas Kell.
********************************************************************
*Douglas B. Kell                            Phone: +44 1970 622334 *
*Edward Llwyd Building                      Fax:   +44 1970 622354 *
*Institute of Biological Sciences                                  *
*University of Wales,                        Email: dbk@aber.ac.uk *
*Aberystwyth SY23 3DA, U.K.  http://gepasi.dbs.aber.ac.uk/home.htm *
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From owner-biophysics@net.bio.net Wed Oct 08 23:00:00 1997
Path: biosci!daresbury!not-for-mail
From: <RUMYM@BGEARN.ACAD.BG>
Newsgroups: bionet.biophysics
Subject: Donnan potential  (Pentcho Valev)
Date: 9 Oct 1997 15:47:17 +0100
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I would like to inform the group that Herman Berendsen from Groningen
kindly agreed to help me in measuring Donnan potential far from the
membrane, in both directions, in different ways. If the potential is
as thermodynamics predicts, I would apologize to the group for wasting
so much time and archive space. However if the potential approaches
zero with distance (as in the book Bill Tivol cited), I would ask
bioenergeticists to take part in building a new theoretical foundation.
This is not so dangerous - much more stable theoretical constructs
have been demolished, replaced, developed etc. Aut inveniam viam
aut faciam (I shall either find the road or make it).

Best regards,
Pentcho

From owner-biophysics@net.bio.net Wed Oct 08 23:00:00 1997
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From: Wyling Com <wyling@consultation.net>
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Want to apply for green card through National Interest Waiver by
Yourself? Send e-mail to wyling@consultation.net.

From owner-biophysics@net.bio.net Wed Oct 08 23:00:00 1997
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From: prismx@earthlink.net (Claire Haller)
Newsgroups: bionet.neuroscience,bionet.biophysics,bionet.cellbiol
Subject: SCIENCE-WEEK: This Week's Headlines (10 Oct 97)
Date: Thu, 09 Oct 1997 16:20:49 GMT
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Headlines in This Week's SCIENCE-WEEK (October 10, 1997)
[complete news reports free at http://members.aol.com/sciweek]

1. More Criticism of the Peer Review Process
2. A Cloning Moratorium by U.S. Biologists
3. Continuing Problems of Genome Patenting
4. Head of NIH Comments on Clinical Studies in Third World
5. Identification of Possibly the Most Luminous Star Known
6. A New Commercial Venture to Sell Asteroid Data
7. The Origin of Earth's Moon
8. A New Model for Earth's Magnetic Dynamo
9. Purple Bacteria, Quantum Physics, and Photosynthesis
10. Identification of a Mammalian Circadian Rhythm Gene
11. Identification of a Gene for a Key Vitamin D Enzyme
12. Mechanisms of Ligand-Gated Ion Channels
13. Mechanisms of Action of General Anesthetics
14. Identification of Macular Degeneration Gene
15. Alarm Over Chesapeake Bay Dinoflagellate Fish Parasite
16. Evidence for Apparent Smoke Resistance in Asian Arteries

The Editors
SCIENCE-WEEK
A Free Weekly Digest of the News of Science
prismx@earthlink.net
http://members.aol.com/sciweek


From owner-biophysics@net.bio.net Thu Oct 09 23:00:00 1997
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From: www@MAIL.CRYST.BBK.AC.UK (Dave Houldershaw)
Newsgroups: bionet.biophysics
Subject: Protein Crystallography on the Web
Date: 10 Oct 1997 11:52:16 -0700
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Protein Crystallography on the Web '97/'98
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From owner-biophysics@net.bio.net Thu Oct 09 23:00:00 1997
Path: biosci!MAILGATE.SURFONAIR.CO.UK!agarcia
From: agarcia@MAILGATE.SURFONAIR.CO.UK
Newsgroups: bionet.biophysics
Subject: Re: Donnan potential (Pentcho Valev)
Date: 10 Oct 1997 09:48:24 -0700
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how can I subscribe to this list and to bio-soft? thanks in advance. 
have a nice weekend
> To:            biophys@net.bio.net
> From:          <RUMYM@BGEARN.ACAD.BG>
> Subject:       Donnan potential (Pentcho Valev)
> Date:          5 Oct 1997 12:51:18 +0100

> Jonathan Marder wrote:
> Pentcho, here is the crux of the problem. It is fine by me if you take  <
> the "infinity point" as potential zero, but you can only do that for ONE<
> side of the membrane. Actually, in practice, since the space enclosed by<
> a membrane is finite, there is no infinity point inside a membrane      <
> vesicle.                                                                <
> 
> Yes here is the crux of the problem. But why should we change the system?
> Let us solve first the problem for the case in which the right and left
> side of the membrane have "equal rights", i.e. for the system
> 
>      10 mM KCl                   M                 1 mM KCl
> 
> where M is a membrane permeable only to K+.
>    Do you agree that, at equilibrium, the potential difference between
> points symmetrical with respect to but distant enough from the membrane
> is zero? If yes, we will go immediately to the "vesicle" case - it is
> more complicated but more interesting of course.
> 
> Pentcho
> 
> 

From owner-biophysics@net.bio.net Thu Oct 09 23:00:00 1997
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From: Zanfir's <zamfirv@interlog.com>
Newsgroups: bionet.biophysics
Subject: Who belives in The Philidalphia expirement?
Date: Fri, 10 Oct 1997 00:26:19 -0400
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--------------B77FF0DD8BCE2092E9C95114
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Hi, I was wondering if any one believes in the Philadelphia experiment
and if they had info on it? if you don't know what im talking about its
about the experiment Albert Einstein did with a ship, which was
transported from one place to another.

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From owner-biophysics@net.bio.net Fri Oct 10 23:00:00 1997
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From: "Bryan L. Brown" <idaho@appstate.campus.mci.net>
Newsgroups: bionet.biophysics
Subject: Re: Equation for plant growth
Date: Sat, 11 Oct 1997 01:18:33 -0000
Organization: CampusMCI
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None that I know of have been very widely accepted.  There are a few
speculative equations out there but they are all attempting to generalize
across an extremely broad range of organisms and I doubt any equation could
seriously attmept to do so.  Most of the equations of the sort are organism
specific or simply generalized models interested in making a particular
point.  If you do find what you think you're looking for, be wary.

drake@erols.com wrote in message <3436A9F6.2AF1@erols.com>...
>Have the results of any research been used to formulate an
>equation for plant growth?  For example, the basic "water + CO2 +
>light energy = growth" formula; has there ever been a calculated ratio
>of CO2/light energy (x amount CO2/y amount of lumens, for example)?
>     If such a ratio and equation do exist, have any been formulated
>that take into account temperature and nutrients?  For instance, in
>the above equation iron would play a role.
>     Any help with finding this information would be greatly
>appreciated.  Thank you.



From owner-biophysics@net.bio.net Fri Oct 10 23:00:00 1997
Path: biosci!agate!newsgate.duke.edu!nntprelay.mathworks.com!howland.erols.net!newspump.sol.net!newsspool.sol.net!newspump.wustl.edu!fas-news.harvard.edu!mlevin
From: mlevin@login5.fas.harvard.edu (Michael Levin)
Newsgroups: bionet.biophysics,bionet.cellbiol,bionet.molbio.methds-reagnts,sci.engr.biomed,sci.med
Subject: looking for slippery, permeable, artificial membrane
Date: 11 Oct 1997 22:32:42 GMT
Organization: Harvard University, Cambridge, Massachusetts
Lines: 14
Message-ID: <61ouqa$p7h$1@news.fas.harvard.edu>
NNTP-Posting-Host: login5.fas.harvard.edu
Xref: biosci bionet.biophysics:3602 bionet.cellbiol:8227 bionet.molbio.methds-reagnts:61944


Can someone suggest where I can buy some of the following: a membrane
(artificial) which is slippery and very smooth - so that tissues can grow
and expand on it, and is also permeable to nutrients and other molecules.
Perhaps something like this is used in organ or tissue culture, etc. I am
basically trying to mimic the vitelline membrane covering the chicken
embryo. Chick embryos can be cultured on the vitelline membranes, but it
is a real pain in the butt to deal with the real one out of the egg. It
would make things much easier if I could buy sheets of the stuff, and
culture my embryos on it (laid over albumen). Please email
mlevin@fas.harvard.edu if you have any ideas. Thanks!

Mike Levin


From owner-biophysics@net.bio.net Sat Oct 11 23:00:00 1997
Path: biosci!classic.msn.com!rcb5
From: rcb5@classic.msn.com ("Ronald Blue")
Newsgroups: bionet.biophysics
Subject: RE: looking for slippery, permeable, artificial membrane
Date: 11 Oct 1997 18:39:23 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 30
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <UPMAIL16.199710120137520575@classic.msn.com>
NNTP-Posting-Host: net.bio.net

This may work.  Get a telflon pan, put a negative electrical charge on the
pan and ground the positive.   Pan should be on a rubber mat.  If it does
not work reverse the charge.  Put me in as coinventor if it works and we
will patent it.  50/50 split.  Ron Blue
http://www.neutronicstechcorp.com/private/
>>>>>>>>>>>>>>
----------
From: 	Michael Levin
Sent: 	Saturday, October 11, 1997 6:32 PM
To: 	biophys@net.bio.net
Subject: 	looking for slippery, permeable, artificial membrane


Can someone suggest where I can buy some of the following: a membrane
(artificial) which is slippery and very smooth - so that tissues can grow
and expand on it, and is also permeable to nutrients and other molecules.
Perhaps something like this is used in organ or tissue culture, etc. I am
basically trying to mimic the vitelline membrane covering the chicken
embryo. Chick embryos can be cultured on the vitelline membranes, but it
is a real pain in the butt to deal with the real one out of the egg. It
would make things much easier if I could buy sheets of the stuff, and
culture my embryos on it (laid over albumen). Please email
mlevin@fas.harvard.edu if you have any ideas. Thanks!

Mike Levin






From owner-biophysics@net.bio.net Sat Oct 11 23:00:00 1997
Path: biosci!classic.msn.com!rcb5
From: rcb5@classic.msn.com ("Ronald Blue")
Newsgroups: bionet.biophysics
Subject: FW: looking for slippery, permeable, artificial membrane
Date: 11 Oct 1997 18:45:44 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 40
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <UPMAIL16.199710120144430012@classic.msn.com>
NNTP-Posting-Host: net.bio.net

If you want to watch the nervous system development have a
modulating charge at 30 hertz, 10 hertz, etc...
Ron Blue
>>>>>>>>>>>>
----------
Sent: 	Saturday, October 11, 1997 9:42 PM
To: 	biophys@net.bio.net; Michael Levin
Subject: 	RE: looking for slippery, permeable, artificial membrane

This may work.  Get a telflon pan, put a negative electrical charge on the
pan and ground the positive.   Pan should be on a rubber mat.  If it does
not work reverse the charge.  Put me in as coinventor if it works and we
will patent it.  50/50 split.  Ron Blue
http://www.neutronicstechcorp.com/private/
>>>>>>>>>>>>>>
----------
From: 	Michael Levin
Sent: 	Saturday, October 11, 1997 6:32 PM
To: 	biophys@net.bio.net
Subject: 	looking for slippery, permeable, artificial membrane


Can someone suggest where I can buy some of the following: a membrane
(artificial) which is slippery and very smooth - so that tissues can grow
and expand on it, and is also permeable to nutrients and other molecules.
Perhaps something like this is used in organ or tissue culture, etc. I am
basically trying to mimic the vitelline membrane covering the chicken
embryo. Chick embryos can be cultured on the vitelline membranes, but it
is a real pain in the butt to deal with the real one out of the egg. It
would make things much easier if I could buy sheets of the stuff, and
culture my embryos on it (laid over albumen). Please email
mlevin@fas.harvard.edu if you have any ideas. Thanks!

Mike Levin







From owner-biophysics@net.bio.net Sat Oct 11 23:00:00 1997
Path: biosci!cc.UManitoba.CA!gordonr
From: gordonr@cc.UManitoba.CA (Richard Gordon)
Newsgroups: bionet.biophysics
Subject: Re: looking for slippery, permeable, artificial membrane
Date: 11 Oct 1997 23:06:26 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 35
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <v01530500b065ac2ac4df@[130.179.152.122]>
NNTP-Posting-Host: net.bio.net

Dear Mike,
Thin latex might do the trick. See:

Harris, A.K. (1984). Tissue culture cells on deformable substrata:
biomechanical implications. J. Biomech. Eng.  106(1), 19-24.

Harris, A.K., P. Wild & D. Stopak (1980). Silicone rubber substrata: a new
wrinkle in the study of cell locomotion. Science  208, 177-179.

Lee, A.A., T. Delhaas, L.K. Waldman, D.A. MacKenna, F.J. Villarreal & A.D.
McCulloch (1996). An equibiaxial strain system for cultured cells. Am. J.
Physiol.  271(4 Pt 1), C1400-C1408.
Best, -Dick Gordon

>Can someone suggest where I can buy some of the following: a membrane
>(artificial) which is slippery and very smooth - so that tissues can grow
>and expand on it, and is also permeable to nutrients and other molecules.
>Perhaps something like this is used in organ or tissue culture, etc. I am
>basically trying to mimic the vitelline membrane covering the chicken
>embryo. Chick embryos can be cultured on the vitelline membranes, but it
>is a real pain in the butt to deal with the real one out of the egg. It
>would make things much easier if I could buy sheets of the stuff, and
>culture my embryos on it (laid over albumen). Please email
>mlevin@fas.harvard.edu if you have any ideas. Thanks!
>
>Mike Levin

--------------------------------------------------------------------
Dr. Richard Gordon, Department of Radiology
University of Manitoba, Health Sciences Centre
Rm. A246, 820 Sherbrook Street, Winnipeg, MB R3A 1R9 Canada
Phone: (204) 789-3828,  Fax: (204) 787-2080, Home: (204) 589-0411
E-mail: GordonR@cc.UManitoba.ca



From owner-biophysics@net.bio.net Sat Oct 11 23:00:00 1997
Path: biosci!daresbury!not-for-mail
From: "Rohan H. Wickramasinghe" <rohan@ites.ac.lk>
Newsgroups: bionet.biophysics
Subject: Dielectric constants
Date: 12 Oct 1997 08:47:01 +0100
Organization: Institute for Tropical Environmental Studies
Lines: 38
Sender: lpddist@mserv1.dl.ac.uk
Distribution: bionet
Message-ID: <61pv9l$kfp@mserv1.dl.ac.uk>
Original-To: biophys@dl.ac.uk, biophys@dl.ac.uk

Hello,

Some time back, we presented evidence which supported the
possibility of a novel regulatory mechanism for the
biosynthesis of steroid hormones in the adrenal cortex.

We are writing just now to ask for information as to
developments in instrumentation and techniques for the
estimation of dielectric constants which may have taken place
in recent years and which may be of interest for possible
research studies in this area. The following papers are of
relevance:

1. " Regulation of corticosteroid hydroxylations: the
   intramitochondrial dielectric constant and proteolipids of
   adrenodoxin and cytochrome P450",
   CYTOBIOS (England) 8(1973)81-94,

2. " The regulation of corticosteroid hydroxylations. 1. An
   effect of inorganic ions in regulating iron-sulphur
   protein-dependent electron transport ", JOURNAL OF
   BIOENERGETICS 5(1973)151-161, and

3. " Dielectric constants and lithium ion treatment of
   psychiatric illness ", Abstracts, 35th Annual National Meeting
   of the American Federation for Clinical Research, 30 April -
   1 May 1978 at San Francisco, California,
   CLINICAL RESEARCH 26(1978)297A.

Thank you very much for any help you can give.

Rohan H. Wickramasinghe, Ph.D.,
Institute for Tropical Environmental Studies,
41 Flower Road,
Colombo 7,
Sri Lanka
(e-mail: rohan@ites.ac.lk)


From owner-biophysics@net.bio.net Sat Oct 11 23:00:00 1997
Path: biosci!daresbury!uninett.no!news.maxwell.syr.edu!newsin.agis.net!agis!news2.dearborn.agis.net!agis!usenet
From: 350@364.com
Newsgroups: bionet.biophysics
Subject: NLREG - Nonlinear & linear statistical regression program - 34 1012045452 KMI
Date: Sun, 12 Oct 97 04:55:04
Organization: Nonlinear Regression Software
Lines: 53
Message-ID: <61q6p9$qn1@news2.dearborn.agis.net>
NNTP-Posting-Host: 204.181.142.21

    ** Announcing NLREG -- Nonlinear Statistical Regression Program **

               http://www.sandh.com/sherrod/nlreg.html

NLREG is a powerful statistical analysis program for Windows 95 and NT
that performs linear and nonlinear regression analysis and curve fitting.
NLREG determines the values of parameters for an equation, whose form you
specify, that cause the equation to best fit a set of data values.  NLREG
can handle linear, polynomial, exponential, logistic, periodic, and
general nonlinear functions.

NLREG features a full programming language with a syntax similar to C
for specifying the function that is to be fitted to the data. This allows
you to compute intermediate work variables, use conditionals, and even
iterate in loops.  With NLREG it is easy to construct piecewise functions
that change form over different domains.

NLREG performs true nonlinear regression, it does not transform the
function into a linear form. As a result, it can handle functions that
are impossible to linearize such as:

  Y = Amplitude*SIN(Freq*X+Phase) + A*EXP(X);

Another advantage of handing the function in true nonlinear form is that
the minimization of the sum of squared residual values (i.e., "least
squares") is based on the true nonlinear value rather than some linearized
transformation.

In addition to computing the optimal values of the parameters, NLREG can
generate plots of the data points and the fitted equation. In addition, it
can plot the distribution of residual values.

In addition to performing classic nonlinear regression, NLREG can be used
to find the root or minimum value of a general nonlinear function. It can
also be used in a special form where the independent variable is omitted;
an interesting application of this is "circular regression" where a circle
is fitted to a set of data points.

NLREG is in use at hundreds of universities, laboratories, and government
agencies around the world (including the U.S. Navy, Harvard, and Duke).

The price of NLREG is only $65 ($70 if outside the USA), which is far
below the cost of comparable commercial regression programs.  And you can
download a shareware demonstration version of NLREG to try out before you
decide to purchase it.

To learn more about NLREG and download your free shareware version, visit
the web site:

    http://www.sandh.com/sherrod/nlreg.html

-- 34: bionet.biophysics 1012045452 --


From owner-biophysics@net.bio.net Sun Oct 12 23:00:00 1997
Path: biosci!daresbury!uninett.no!news.maxwell.syr.edu!newsfeed.internetmci.com!152.163.199.19!portc03.blue.aol.com!audrey02.news.aol.com!not-for-mail
From: lbrenne532@aol.com (LBrenne532)
Newsgroups: bionet.biophysics
Subject: For Sale:  Health Physics, Radiation Safety reference materials
Date: 13 Oct 1997 01:04:06 GMT
Lines: 11
Message-ID: <19971013010401.VAA29455@ladder02.news.aol.com>
NNTP-Posting-Host: ladder02.news.aol.com
X-Admin: news@aol.com
Organization: AOL http://www.aol.com

For Sale:

20 boxes of Health Physics, Radiation Safety manuals, texts, etc.
including over 5 years of Health Physics Journal and newsletters.
CRC titles, NRC pubs, ionizing and non-ionizing radiation, etc.
Too many to name here.  Retired from industry after 15 years in
health physics.

US$750 or make offer.  You pay shipping.

E-mail LBrenne532@aol.com for complete list in ASCII.

From owner-biophysics@net.bio.net Mon Oct 13 23:00:00 1997
Path: biosci!fcs280s.ncifcrf.gov!cpk-news-feed4.bbnplanet.com!cpk-news-feed1.bbnplanet.com!cpk-news-hub1.bbnplanet.com!news.bbnplanet.com!www.nntp.primenet.com!globalcenter0!news.primenet.com!nntp.primenet.com!news.asu.edu!general2.asu.edu!cousins
From: cousins@imap3.asu.edu
Newsgroups: bionet.biophysics
Subject: isosbestic wavelengths
Date: Mon, 13 Oct 1997 21:10:11 -0700
Organization: Arizona State University
Lines: 2
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Mime-Version: 1.0
Content-Type: TEXT/PLAIN; charset=US-ASCII
X-Sender: cousins@general2.asu.edu

Help me out if ya would.  What causes pH dyes to emit isosbestic 
wavelengths when excited? Thanks.    

From owner-biophysics@net.bio.net Mon Oct 13 23:00:00 1997
Path: biosci!bcm.tmc.edu!news.msfc.nasa.gov!newsfeed.internetmci.com!199.60.229.5!newsfeed.direct.ca!news.uoregon.edu!oregon.uoregon.edu!MAYNARD
From: maynard@oregon.uoregon.edu (Tom Maynard)
Newsgroups: bionet.biophysics,bionet.cellbiol,bionet.molbio.methds-reagnts,sci.engr.biomed,sci.med
Subject: Re: looking for slippery, permeable, artificial membrane
Date: 14 Oct 1997 02:22:13 GMT
Organization: University of Oregon, Eugene, Oregon
Lines: 18
Message-ID: <61ul0l$edp$1@pith.uoregon.edu>
References: <61ouqa$p7h$1@news.fas.harvard.edu>
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Xref: biosci bionet.biophysics:3609 bionet.cellbiol:8233 bionet.molbio.methds-reagnts:61977

In article <61ouqa$p7h$1@news.fas.harvard.edu>, mlevin@login5.fas.harvard.edu (Michael Levin) writes:
>
>Can someone suggest where I can buy some of the following: a membrane
>(artificial) which is slippery and very smooth - so that tissues can grow
>and expand on it, and is also permeable to nutrients and other molecules.
>Perhaps something like this is used in organ or tissue culture, etc. 

Millipore makes tissue culture plate inserts, with different types of filter
material and different pore sizes, that can be inserted into dishes for
culturing cells.  It's called "Millicell" in their catalog, and there are
quite a few different types (size, pore size, filter type).

Someone in our lab successfully used them for coculture experiments a while
back, for what it's worth..

--Tom Maynard
  Lab Slave


From owner-biophysics@net.bio.net Mon Oct 13 23:00:00 1997
Path: biosci!bloom-beacon.mit.edu!howland.erols.net!newsfeed.internetmci.com!152.163.199.19!portc03.blue.aol.com!audrey01.news.aol.com!not-for-mail
From: huntpharm@aol.com (Huntpharm)
Newsgroups: bionet.biophysics
Subject: US-MD-JOB OPPORTUNITY IN CELL CULTURE
Date: 14 Oct 1997 12:49:41 GMT
Lines: 12
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NNTP-Posting-Host: ladder01.news.aol.com
X-Admin: news@aol.com
Organization: AOL http://www.aol.com

I am looking for a Research Technician to perform cell culture.  This person
 will be working on a project in cancer and your responsibilities will be to
 perform cell culture (maintain stable cell lines), perform some basic
 molecular biology (northern, southern and western blots), as well as, some
 animal handling and injections.  The candidate should possess a B.S. or
 M.S.degree.  We are a leading biotech firm with research facilities in
 Baltimore, Maryland and can provide excellent benefits (health insurance,
 dental, and vision plan, paid vacation and more). A high impact, high profile
 position with excellent opportunity for advancement.  Please contact Scott
 Shanes by phone at 609-584-8733 Ext. 218, fax resume and cover letter to
 609-584-9575 or E-Mail to sis@dmc10.com or sis@diedremoire.com


From owner-biophysics@net.bio.net Mon Oct 13 23:00:00 1997
From: huntpharm@aol.com (Huntpharm)
Newsgroups: bionet.biophysics
Subject: US-MD-JOB OPPORTUNITY IN QUALITY ASSURANCE
Date: 14 Oct 1997 12:49:00 GMT
Lines: 18
Message-ID: <19971014124900.IAA06228@ladder02.news.aol.com>
NNTP-Posting-Host: ladder02.news.aol.com
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Path: biosci!news.ic.sunysb.edu!news-pen-15.sprintlink.net!newsfeed.nysernet.net!news.nysernet.net!207.41.200.131!news-pen-1.sprintlink.net!news-east.sprintlink.net!news-dc-26.sprintlink.net!news-peer.sprintlink.net!news.sprintlink.net!Sprint!newsfeed.internetmci.com!152.163.199.19!portc03.blue.aol.com!audrey02.news.aol.com!not-for-mail

I am looking for a Scientist to work in Quality Assurance.  This person will
 develop and validate analytical methods related to NDA commitments and foreign
 registry requirements for its products.  The candidate will be responsible for
 providing guidance and leadership to QC analysts in method improvement,
 enhancement and transfer; managing cross validation of analytical methods;
 preparing reports and maintaining laboratory notebooks according to cGMP's and
 established SOP's; and supervising QC analysts.  The position requires a Ph.D.
 with 1-4 years experience in the pharmaceutical industry or an MS with a
 minimum of 6 years in the pharmaceutical industry.  Candidates must have
 knowledge of cGMP's and strong background in all analytical techniques;
 chromatography experience is needed.   We are a leading biotech firm with
 research facilities in Baltimore, Maryland and can provide excellent benefits
 (health insurance, dental, and vision plan, stock options, bonus program, paid
 vacation and more). A high impact, high profile position with excellent
 opportunity for advancement.  Please contact Scott Shanes by phone at
 609-584-8733 Ext. 218, fax CV and cover letter to 609-584-9575 or E-Mail to
 sis@dmc10.comsis@diedremoire.com


From owner-biophysics@net.bio.net Tue Oct 14 23:00:00 1997
From: villowan@earthlink.net (Charlsie Patterson)
Newsgroups: bionet.biophysics
Subject: Excellent Position in Genetics Initiative
Date: Wed, 15 Oct 1997 12:59:28 GMT
Organization: EarthLink Network, Inc.
Lines: 30
Message-ID: <622eqb$h4u@suriname.earthlink.net>
NNTP-Posting-Host: 38.30.41.226
X-Newsreader: Forte Free Agent 1.0.82
Path: biosci!news.ic.sunysb.edu!news-pen-15.sprintlink.net!newsfeed.nysernet.net!news.nysernet.net!207.41.200.131!news-pen-1.sprintlink.net!news-east.sprintlink.net!news-dc-26.sprintlink.net!news-peer.sprintlink.net!news-peer-east.sprintlink.net!news.sprintlink.net!Sprint!news.idt.net!cam-news-hub1.bbnplanet.com!news.bbnplanet.com!prodigy.com!nntp.earthlink.net!usenet

This is a permanent position with a huge multinational Pharmecuetical
company. Excellent pay and benefits along with unlimited growth
potential.  Our client company is agressivly seeking to fill this
position and will be covering all fees as well as relocation for a
suitable candidate.  If qualified and interested, please contact:

Charlsie Patterson
Global Staffing and Recruiting
villowan@earthlink.net
or phone: (919) 871-0070
or fax credentials to:
(919) 871-0030


Consultant:  Genetic Initiative

Summary of duties:  Perform statistical analysis of data generated in
support of  company's Genetic Initiative.  Develop and improve
existing analysis software.  Interact with researchers in growing
Genetic Initiative to define and implement genetics strategy.
Evaluate statistical aspects of new technologies.

Minimum Qualifications: Ph.D. in statistics or quantitative genetics
with some applied analysis experience. Genetics background is
essential.  Experience with UNIX file systems and SAS or other
statistical analysis package required.  Excellent teamwork,
interpersonal and communication skills are necessary.




From owner-biophysics@net.bio.net Tue Oct 14 23:00:00 1997
Path: biosci!daresbury!not-for-mail
From: <33879476@prodigy.com>
Newsgroups: bionet.biophysics
Subject: (guest) TONER
Date: 15 Oct 1997 05:03:47 +0100
Lines: 49
Sender: lpddist@mserv1.dl.ac.uk
Distribution: bionet
Message-ID: <621fb3$a6k@mserv1.dl.ac.uk>
Original-To: friend@piblic.com




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From owner-biophysics@net.bio.net Tue Oct 14 23:00:00 1997
Path: biosci!daresbury!uninett.no!newsfeed.nacamar.de!news-feed.inet.tele.dk!news.misty.com!nntp.upenn.edu!axe1.med.upenn.edu!axelsen
From: axelsen@axe1.med.upenn.edu (Paul H Axelsen)
Newsgroups: bionet.biophysics
Subject: POSTDOCTORAL POSITIONS AVAILABLE: Molecular Recognition and Membrane Biophysics
Date: 15 Oct 1997 22:33:37 GMT
Organization: University of Pennsylvania
Lines: 45
Message-ID: <623gc1$584$11@netnews.upenn.edu>
NNTP-Posting-Host: axe1.med.upenn.edu
X-Newsreader: TIN [version 1.2 PL2-upenn1.1]

POSTDOCTORAL POSITIONS AVAILABLE: Molecular Recognition and Membrane Biophysics

Location:    Department of Pharmacology
             University of Pennsylvania
             Philadelphia, Pennsylvania, USA

Projects include studies of antibiotics, fusogenic peptides, and blood 
coagulation proteins on lipid membranes - using novel spectroscopic 
(infrared and UV), computational, and mass spectrometric techniques - with
a view towards rational drug design.

The positions are stably funded and available immediately.

Requirements:   Strong background in chemistry and biology (at least some
                  background in both fields required, i.e. biochemstry or
                  biological chemistry - physics is also very helpful)
                Doctoral degree (Ph.D., M.D., D.Sc., or equivalent)
                Minimum 2 year committment
                Talent for mastering sophisticated new technology
                Interest in working on important biomedical problems
 

Some general information about the lab is available at http://axe2.med.upenn.edu

Interest persons should inquire by email to    axe@pharm.med.upenn.edu

or write/call:

Prof. Paul H. Axelsen
Departments of Pharmacology and
  Medicine, Infectious Diseases Section
University of Pennsylvania
Rooms 130/131 John Morgan Bldg
3620 Hamilton Walk
Philadelphia, PA 19104-6084

215-898-9238 / 9766 (tel)
215-573-2236 (fax)


--

------------------------------------------------------------------------------
                                                                              
Axe@pharm

From owner-biophysics@net.bio.net Tue Oct 14 23:00:00 1997
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From: azereza <azereza@hotmail.com>
Newsgroups: bionet.biophysics
Subject: Could U help me?
Date: Wed, 15 Oct 1997 19:23:53 +0000
Organization: NetSat Inc.
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I'm trying hard to translate this text to English, but it seems not
work.
 Could you plz correct it for me? I have to present this by noon
tomorrow.
 Here is the part I have problem.

 The linear DC power is capable of supplying the DC Voltage from 0 to
+30 Volt and 0 to -30 Volt ( providing 1 ampere current at most ), and
of 5 Volt Voltage supply ( providing 2 ampere current at most ).

 The section of  the linear DC power providing the DC Voltage from 0 to
 +30 Volt and 0 to -30 Volt is designed without using processed IC
whileas
 the design of the section providing 5 Volt Voltage supply includes IC
 regulator and short-circuit protection. The intent here is to prevent 
 any damages that may occur with the linear DC power generator. This
 DC power supply also includes the over-voltage protection to protect
 the damage which may occur with any devices in the circuit or the
damages in the circuit itself.

REPLY TO: u3811771@student.chula.ac.th

Thanx in advance!
Maia

From owner-biophysics@net.bio.net Tue Oct 14 23:00:00 1997
Path: biosci!UCONNVM.UCONN.EDU!RHODES
From: RHODES@UCONNVM.UCONN.EDU
Newsgroups: bionet.biophysics
Subject: Abstract sponsor???
Date: 15 Oct 1997 08:41:50 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 27
Sender: daemon@net.bio.net
Distribution: world
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NNTP-Posting-Host: net.bio.net

OK - I don't know whether such "solicitation" is frowned upon, but I'll
     give it a shot - if you can help, I'd appreciate it.

I have materials that students would like to see presented at the
Kansas City meetings, but the students will not be able to attend
(due to course conflicts and $ - in both cases).  I also have an
abstract that needs to be approved by a collaborator/company, and
the turnaround is very slow - (read as "will not know by today but
most likely will know before 24th").  Thus, I would like to be
able to get >1 poster submitted but the students in question are
nonmembers.  The question is:

<<<bottom line here>>>
Is there anyone out there who is a member and is not planning to
submit a paper or sponsor one, and is willing to lend his/her name
to our work?  I'd appreciate it.

(PS - if the society admin./exec. readers don't like the idea
of "soliciting," please let me know so I can post a retraction.)

|                             O==O                            |
| David G. Rhodes             O==O  Phone 860-486-5413        |
| School of Pharmacy; U-92    O==O  Fax   860-486-4998        |
| University of Connecticut   O==O                            |
| Storrs, CT  06269-2092      O==O  rhodes@uconnvm.uconn.edu  |
|_____________________________O==O____________________________|
    CAUTION: Dates on calendar are closer than they appear!

From owner-biophysics@net.bio.net Wed Oct 15 23:00:00 1997
Path: biosci!rutgers!nntp.upenn.edu!newsserver.jvnc.net!news.pn.com!nntp.pn.com!main.Germany.EU.net!main.de.uu.net!fu-berlin.de!news-peer.gsl.net!news.gsl.net!gip.net!news-peer.sprintlink.net!news.sprintlink.net!Sprint!newsfeed.internetmci.com!205.219.166.144!banzai!swen.emba.uvm.edu!elk.uvm.edu!hbeernin
From: hbeernin@elk.uvm.edu (Hans Beernink)
Newsgroups: bionet.biophysics,bionet.cellbiol,bionet.molbio.methds-reagnts,sci.engr.biomed,sci.med
Subject: Re: looking for slippery, permeable, artificial membrane
Followup-To: bionet.biophysics,bionet.cellbiol,bionet.molbio.methds-reagnts,sci.engr.biomed,sci.med
Date: 16 Oct 1997 02:53:19 GMT
Organization: University of Vermont
Lines: 17
Message-ID: <623viv$3pk@swen.emba.uvm.edu>
References: <61ouqa$p7h$1@news.fas.harvard.edu> <61ul0l$edp$1@pith.uoregon.edu>
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Xref: biosci bionet.biophysics:3619 bionet.cellbiol:8248 bionet.molbio.methds-reagnts:62041

Tom Maynard (maynard@oregon.uoregon.edu) wrote:
: In article <61ouqa$p7h$1@news.fas.harvard.edu>, mlevin@login5.fas.harvard.edu (Michael Levin) writes:
: >
: >Can someone suggest where I can buy some of the following: a membrane
: >(artificial) which is slippery and very smooth - so that tissues can grow
: >and expand on it, and is also permeable to nutrients and other molecules.
: >Perhaps something like this is used in organ or tissue culture, etc. 

and what about soluble collagen for TC?  two options for this one- 1) a 
gel (approx. 0.3- 2mm thick) which mimics a dermal matrix, and 2) a thin 
layer (e.g. thickness of a few molecules or so) that provides a surface 
for attachment.  Either might be suitable for your expts, although you're 
not very explicit about your needs.

Best,
Hans


From owner-biophysics@net.bio.net Thu Oct 16 23:00:00 1997
Path: biosci!internet!biosci!not-for-mail
From: biohelp (BIOSCI Administrator)
Newsgroups: bionet.biophysics
Subject: BIOSCI/bionet miniFAQ & Fundraiser
Date: 17 Oct 1997 02:00:06 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 233
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199710170900.CAA09440@net.bio.net>
NNTP-Posting-Host: net.bio.net

(LAST REVISION: 30-JUL-95)

This BIOSCI "miniFAQ" is designed to answer the questions that come up
the *most frequently*.  The main BIOSCI FAQ (Frequently Asked
Questions) is accessible on the World Wide Web at URL
http://www.bio.net/.

If you can not find an answer to your question in this or other
documentation, the BIOSCI technical support staff answers e-mail
queries sent to

		       biosci-help@net.bio.net

We can only answer questions about the use of the newsgroups and
mailing lists.  We unfortunately do not have the staff to do Internet
information searches or answer scientific questions.  Please post
those to the appropriate BIOSCI/bionet newsgroups.


	Contents:
	--------
	0) BIOSCI NEEDS YOUR SUPPORT!!

	1) Using the WWW to access the BIOSCI/bionet newsgroups.

	2) What to do about "spams," i.e., junk mail, ads, etc.

	3) Examples of subscribing and unsubscribing to the mailing lists.

	4) The BIOSCI user address and research interest directory.


0) BIOSCI NEEDS YOUR SUPPORT!!
------------------------------
BIOSCI's government funding has been expended, and we are now
operating solely from advertising revenue that we have raised from our
Web site at http://www.bio.net/.  We need just a few minutes of your
time to help us serve you.

You can do two important things which will take very little time for
you individually and will immensely help us continue to help you.

First, please use our WWW system at http://www.bio.net/ to access the
archives.  You can post or reply to messages via your Web browser as
described in item #1 below.  Your usage helps attract sponsors. If you
contact any of our sponsors, please be sure to thank them for
supporting BIOSCI. It is critical for them to get this feedback if
they are to continue their sponsorship for the long term.

Second, if you work for a company or organization that provides
products or services of interest to the biology community, please pass
this message on to your marketing or marketing communications
department or other appropriate group.  Please ask them to help
support BIOSCI by sponsoring our Web site and explain the uses and
benefits of the system to the biology community. If they are
interested, they can then contact us for further information at our
tech support address, biosci-help@net.bio.net.


1) Using the WWW to access the BIOSCI/bionet newsgroups.
--------------------------------------------------------
As of 10 December 1995, all BIOSCI/bionet full newsgroups are
accessible through the World Wide Web (WWW) at URL http://www.bio.net.
One can read and reply publicly or privately to both recent postings
and archived messages through one's Web browser if it is configured
properly to send e-mail.  Each newsgroup is equipped with its own WAIS
index.  The main BIOSCI home page also has access to the BIO-JOURNALS
Table of Contents database WAIS index and the BIOSCI user address
database described in another item further below.


2) What to do about "spams," i.e., junk mail, ads, etc.
-------------------------------------------------------
BIOSCI is a set of parallel USENET newsgroups (the "bionet" groups),
mailing lists, and a hypermail archive at URL http://www.bio.net/.
The same postings are distributed on all media (except for a small
number of mailing-list-only groups at net.bio.net).  Unfortunately it
is becoming a despicable practice on the Internet (by a few people out
to make a fast buck) to do automated mass postings to thousands of
newsgroups and mailing lists.  These attempts to grab free advertising
are refered to as "spams" in the usual, somewhat boneheaded, net
terminology.  USENET is more susceptible to this practice, and many
spams originate on the USENET groups and then are passed on to the
mailing lists.  However, spammers also get lists of mailing addresses
and hit these too, so neither medium is immune.

What should you do personally if you get junk mail?
---------------------------------------------------
Just delete it and move on without reading it further.  Filing a
protest is becoming increasingly useless because spammers are often
disguising the addresses where the messages are sent from.  Unless you
really understand Internet mail systems, your attempt at protest by
sending replies to the message will often end up being sent to the
address of an innocent person that the spammer is victimizing.

What can BIOSCI/bionet do to protect its newsgroups?
----------------------------------------------------
The only solution currently available is to moderate the newsgroup.
If this newsgroup is already moderated, then you are in good shape.
Moderation protects the USENET distribution from about 95% of the
spams that are being sent to date and protects the mailing lists
completely.  Moderation means, however, that someone has to take the
time to review each message before it goes out.  We have set up
software here that simply allows the moderator to forward to an
address at net.bio.net messages that (s)he wishes to have distributed.
This takes no more time than that needed to read the message and pass
it on, say about 1 min. per message.

Most newsgroups currently have a discussion leader who is responsible
for their newsgroup.  The discussions leaders and their e-mail
addresses are listed in the BIOSCI Information Sheet which is
available on the Web at http://www.bio.net/.  If a newsgroup is being
hit with too many junk postings, please contact the discussion leader
for that group and see if there is interest in moderating the group.
Please do not assume that by simply posting a complaint to the
newsgroup itself, anyone on the BIOSCI staff will act on your
complaint.  With close to 100 newsgroups to run, the BIOSCI staff has
to rely on the discussion leaders of each newsgroup to report problems
directly to us at biosci-help@net.bio.net.

We will moderate any of our newsgroups if the discussion leader tells
us that the readership of the group wishes to do so and if a moderator
is willing to do the work.  For most BIOSCI/bionet groups, this
entails only a few minutes of work each day.

Moderating a newsgroup will resolve probably 95% of the junk postings
on the USENET distribution.  Unfortunately there are easy ways for
determined spammers to override the moderation mechanism on USENET,
but we can protect our e-mail subscribers from unwanted postings if
the newsgroup is moderated.  You can also access our newsgroups over
the WWW at URL http://www.bio.net.  While this Web interface will not
stop spammers from trying to post to the groups, this will give you
yet another way, besides using USENET news, to keep the junk out of
your personal mail files.  For those of you with local USENET news
systems, the Web interface will also give you faster access to new
newsgroups and recent postings.


3) Examples of subscribing and unsubscribing to the mailing lists.
------------------------------------------------------------------
PLEASE NOTE: The BIOSCI management does NOT act on
subscription/unsubscription requests that are posted improperly to the
newsgroups and mailing lists.  People who do this only bother everyone
on the lists to no avail.  Please be sure to follow the proper
procedures below.

Gory details are in the BIOSCI Information sheets on the Web at
http://www.bio.net.  Below we give an example utilizing the
METHODS-AND-REAGENTS list at both of our two BIOSCI sites:

Users in the Americas and Pacific Rim countries who use the BIOSCI
------------------------------------------------------------------
node at computer net.bio.net:
----------------------------

A) Determine the "listname" which is the <=8 character mail address
                                         ^^^^^^^^^^^^^
   for the group.  These can be found in the BIOSCI Info. Sheet.  For
   the METHODS-AND-REAGENTS group the mailing address is
   methods@net.bio.net.  The listname is the portion of the address to
   the left of the @ sign, i.e., "methods".  The listname is used with
   the "subscribe" and "unsubscribe" commands illustrated below.

B) Mail all commands in the body of a mail message addressed to
   biosci-server@net.bio.net.  Do NOT send commands to the newsgroup
   posting addresses!  Leave the Subject: line blank, any text on it
   will be ignored.

C) In the body of your message put one or more of the following
   commands with an "end" command on the last line, e.g.,

   subscribe methods
   unsubscribe methods
   end

   Do NOT put your e-mail address or other text on these lines.  The
   server only allows you to cancel your subscription if the address
   on your mail header matches the address on our mailing list.
   Please ask for help at biosci-help@net.bio.net if your address has
   changed, e.g., if you know you are on the list but the server tells
   you that you are not a member.


Users in Europe, Africa, and Central Asia who use the BIOSCI node at
--------------------------------------------------------------------
computer daresbury.ac.uk (also known as dl.ac.uk):
-------------------------------------------------

To subscribe and unsubscribe to/from the BIOSCI lists, you need to
specify the full USENET newsgroup name with "bionet-news." prepended.
The USENET newsgroup names are listed in the BIOSCI Information sheet
on the Web at http://www.bio.net/.  For the METHODS-AND-REAGENTS list
the USENET newsgroup name is bionet.molbio.methds-reagnts, thus the
appropriate commands are

    sub bionet-news.bionet.molbio.methds-reagnts

    unsub bionet-news.bionet.molbio.methds-reagnts

These commands are included in a message addressed to mxt@dl.ac.uk,
NOT to the newsgroup mailing addresses.  As usual, include the text in
the body of the message as text on the Subject: line is ignored.

To unsubscribe from all the lists at the UK node, use

    unsub bionet-news

Please note that if the address in the list is different than the one
in your mail message header, you will not be able to unsubscribe by
this method. If you have problems, please mail biosci@daresbury.ac.uk.


4) The BIOSCI user address and research interest directory.
-----------------------------------------------------------
Please take this opportunity to add your name, address, and research
interest information to the BIOSCI User Address Database if you have
not already done so.

You can fill out the address form directly through our Web page at URL
http://www.bio.net/adrform.html.

The address database is reindexed nightly for WWW access (the URL is
http://www.bio.net/).  If you are not directly on the Internet but can
reach it by e-mail, please use our waismail server to access the user
directory.  waismail use is described above.  You can also request a
user address form by e-mail from biosci-help@net.bio.net.

Please check your database entry from time-to-time to see if your
address information is still up-to-date.  Because of our limited
personnel resources, we ask that you resubmit a *complete* form to
revise your entry; we only replace complete entries and do not have
resources to edit old forms.


From owner-biophysics@net.bio.net Thu Oct 16 23:00:00 1997
Path: biosci!agate.berkeley.edu!howland.erols.net!news.maxwell.syr.edu!news-feed1.tiac.net!news-master.tiac.net!news@tiac.net
From: Property Digest <propdig@barryinc.com>
Newsgroups: bionet.biophysics
Subject: National Biotech Register(NatBio)
Date: Fri, 17 Oct 1997 08:51:39 -0700
Organization: U.S. Real Estate Register
Lines: 5
Message-ID: <3447898B.183@barryinc.com>
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NatBio has added a new page to our web site; 
http://www.barryinc.com/bio
This new page allows companies in the Biotech Industries to announce new
products and developments.  NatBio also has a page showing job listings 
in the Biotech fields, as well as a calendar of events page.

From owner-biophysics@net.bio.net Fri Oct 17 23:00:00 1997
Path: biosci!agate!spool.mu.edu!uwm.edu!vixen.cso.uiuc.edu!news-peer.sprintlink.net!news.sprintlink.net!Sprint!news.maxwell.syr.edu!cam-news-hub1.bbnplanet.com!news.bbnplanet.com!prodigy.com!nntp.earthlink.net!usenet
From: prismx@earthlink.net (Claire Haller)
Newsgroups: bionet.neuroscience,bionet.biophysics,bionet.cellbiol
Subject: SCIENCE-WEEK: This Week's Headlines (17 Oct 97)
Date: Sat, 18 Oct 1997 16:24:57 GMT
Organization: SCIENCE-WEEK
Lines: 22
Message-ID: <62ao17$1f3@argentina.earthlink.net>
Reply-To: prismx@earthlink.net
NNTP-Posting-Host: 153.36.138.177
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Xref: biosci bionet.neuroscience:20558 bionet.biophysics:3622 bionet.cellbiol:8260

Headlines in This Week's SCIENCE-WEEK (October 17, 1997)

For free Email subscription to complete news reports,
send SUB SW to prismx@earthlink.net

1. A Conflict Between Seismologists and Defense Analysts
2. An Essay on the Confusion Over Cloning
3. Revelations Concerning Lisa Meitner and the Nobel Prize
4. A Postulate of Possible Sub-Surface Planetary Life Habitats
5. Squeezed Light Experiments Reveal Non-Classical Correlations
6. New Satellite Data Maps the Ocean Floor
7. Gravito-Optical Surface Trap for Super-Cooled Atoms
8. Reversible Metallic State Tuning of Quantum Dot Monolayers
9. Method for Controlled Elaboration of Macromolecular Dendrimers
10. An Unusual Idea Concerning Honeybees and Quarks

The Editors
SCIENCE-WEEK
A Free Weekly Digest of the News of Science
prismx@earthlink.net
http://members.aol.com/sciweek


From owner-biophysics@net.bio.net Sat Oct 18 23:00:00 1997
From: Anindya Bhattachrya <ab4@acsu.buffalo.edu>
Newsgroups: bionet.biophysics
Subject: Noise Analysis
Date: Sat, 18 Oct 1997 21:56:38 -0400
Organization: SUNY Buf.
Lines: 6
Message-ID: <344968D6.1B4F@acsu.buffalo.edu>
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Path: biosci!news.ic.sunysb.edu!news-pen-15.sprintlink.net!newsfeed.nysernet.net!news.nysernet.net!207.41.200.131!news-pen-1.sprintlink.net!news-east.sprintlink.net!news-dc-26.sprintlink.net!news-peer.sprintlink.net!news-sea-19.sprintlink.net!news-in-west.sprintlink.net!news.sprintlink.net!Sprint!128.226.1.24!bingnews.binghamton.edu!news.acsu.buffalo.edu!acsu.buffalo.edu!not-for-mail

Hi ,

	What is a good program that I can use for noise analysis on 
whole cell calcium currents (Mac Preferable, but PC based software 
suggestions also welcome).
		Anindya

From owner-biophysics@net.bio.net Sat Oct 18 23:00:00 1997
Path: biosci!news.ohsu.edu!not-for-mail
From: Matt Jones <jonesmat@ohsu.edu>
Newsgroups: bionet.biophysics
Subject: Re: Noise Analysis
Date: 19 Oct 1997 19:12:34 GMT
Organization: Vollum Institute
Lines: 16
Distribution: world
Message-ID: <62dm32$f06$1@fremont.ohsu.edu>
References: <344968D6.1B4F@acsu.buffalo.edu>
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X-XXDate: Mon, 19 Oct 1987 20:23:23 GMT

In article <344968D6.1B4F@acsu.buffalo.edu> Anindya Bhattachrya,
ab4@acsu.buffalo.edu writes:
>Hi ,
>
>	What is a good program that I can use for noise analysis on 
>whole cell calcium currents (Mac Preferable, but PC based software 
>suggestions also welcome).

I've used AxoGraph (Axon Instruments) on the Mac for non-stationary noise
analysis. It's a pretty nice all-around time-series analysis package. I
imagine you can use it for finding power spectra too, but I haven't done
that.  

Cheers,

Matt

From owner-biophysics@net.bio.net Sun Oct 19 23:00:00 1997
Path: biosci!agate!spool.mu.edu!uwm.edu!www.nntp.primenet.com!globalcenter0!news.primenet.com!nntp.primenet.com!cpk-news-hub1.bbnplanet.com!cam-news-hub1.bbnplanet.com!news.bbnplanet.com!prodigy.com!nntp.earthlink.net!usenet
From: kshreder@znet.com
Newsgroups: bionet.biophysics
Subject: Updated WWWsite:  The Antibody Resource Page
Date: Sun, 19 Oct 1997 16:59:16 -0700
Organization: The Antibody Resource Page
Lines: 62
Message-ID: <344A9ED4.2B02@znet.com>
Reply-To: kshreder@znet.com
NNTP-Posting-Host: 153.35.103.118
Mime-Version: 1.0
Content-Type: text/plain; charset=iso-8859-1
Content-Transfer-Encoding: 8bit
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Updated WWWsite:  The Antibody Resource Page

The Antibody Resource Page has been recently updated.  The page will be
invaluable to researchers and educators alike.

Here is just some of what can be found on the page:

1. How to Find an Antibody - a variety of ways on and off the web to
find the antibody you are looking for.

2. Online Companies - links to over 110 companies that sell antibodies
or antibody related products.  Is your company listed on this page?

3. Antibody Image Gallery - some animated gifs have recently been added

4. Bulletin Board - Have a question or have an answer?  Then stop by and
post a message.

5. Educational Resources - a variety of new links have been added. 
There are links to pages on immunochemistry, antibody production, 
autoimmunity, vaccines, immunology and much more.  This page is divided
up into sections on research, educational, and health resources.

...and there is much more.  Check it out at:

http://www.antibodyresource.com/


Ps.  Don’t forget to visit our sponsors, Research Diagnostics, Inc.
(http://www.researchd.com/absort1.htm) and Lab Vision Corporation
(http://www.labvision.com/)!
Updated WWWsite:  The Antibody Resource Page

The Antibody Resource Page has been recently updated.  The page will be
invaluable to researchers and educators alike.

Here is just some of what can be found on the page:

1. How to Find an Antibody - a variety of ways on and off the web to
find the antibody you are looking for.

2. Online Companies - links to over 110 companies that sell antibodies
or antibody related products.  Is your company listed on this page?

3. Antibody Image Gallery - some animated gifs have recently been added

4. Bulletin Board - Have a question or have an answer?  Then stop by and
post a message.

5. Educational Resources - a variety of new links have been added. 
There are links to pages on immunochemistry, antibody production, 
autoimmunity, vaccines, immunology and much more.  This page is divided
up into sections on research, educational, and health resources.

...and there is much more.  Check it out at:

http://www.antibodyresource.com/


Ps.  Don’t forget to visit our sponsors, Research Diagnostics, Inc.
(http://www.researchd.com/absort1.htm) and Lab Vision Corporation
(http://www.labvision.com/)!

From owner-biophysics@net.bio.net Sun Oct 19 23:00:00 1997
Path: biosci!agate!howland.erols.net!newsfeed.nacamar.de!newscore.univie.ac.at!news.iif.hu!news
From: Zsuzsa Sasvari <sasvari@abc.hu>
Newsgroups: bionet.biophysics
Subject: electron microscopy of protein
Date: Mon, 20 Oct 1997 11:34:34 +0200
Organization: ABC
Lines: 15
Message-ID: <344B25AA.5D09@abc.hu>
NNTP-Posting-Host: che-pc09.abc.hu
Mime-Version: 1.0
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X-Mailer: Mozilla 3.03Gold (Win95; I)

Dear...

We have a problem with a large- 65kD,12 nm protein. We have connected
the monomers via their carbohydrate moieties.Judged by size exclusion
chromatography and gel electrophoresis it seems larger than 6 monomer
linked. Better resolution can not be achieved. Activity measurements
showed that presumingly 8 monomer are linked. When we saw the
e.micrograph, the longest white stripes were about 110 nm long. However
we have seen several shorter ones as well....When we enlarged a monomer
sized white blub, it seemed a wunderfull monomer.

Can it be told that all the polimers are 8-9 monomer long but the
shorter ones are curled ?

Or can you suggest a way how the exact size can be determined?

From owner-biophysics@net.bio.net Tue Oct 21 23:00:00 1997
Path: biosci!fcs280s.ncifcrf.gov!cpk-news-feed4.bbnplanet.com!cpk-news-feed1.bbnplanet.com!cpk-news-hub1.bbnplanet.com!news.bbnplanet.com!news-fra.maz.net!news-hh.maz.net!unlisys!news.snafu.de!cs.tu-berlin.de!zrz.TU-Berlin.DE!news-ber1.dfn.de!news-ham1.dfn.de!newsserver.rrzn.uni-hannover.de!not-for-mail
From: Wolfgang Tra