From owner-biophysics@net.bio.net Sat Aug 02 23:00:00 1997
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From: janczek@aol.com (JanCzek)
Newsgroups: bionet.biophysics
Subject: Respirometer for bacteria
Date: 3 Aug 1997 20:08:58 GMT
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Organization: AOL http://www.aol.com


Measuring Respiration of Yeast, Alaga, Bacteria, Insects, Reptiles.
We developed very sensitive O2/CO2 Respirometer which can monitor oxygen
consumption of bacteria or any substance (oxidation)  at the levels of 0.2
uL
O2/hour.
 It was also  used to measure respiration of zebra mussels, water plants,
respiration of seed, insects, vegetables, olive fruits and cherries. It
was
also used to test bacteria growth in fruit juices and bioremediation rate 
of oil spils ( Exxon
Valdez). 1 to 80 samples can be tested simultaneously over minutes or
months.
Optiona; sensor alow mesurements of CH4,H2S,NH3, H2,CO

If you are interested in receiving more information with published papers
on applications  drop me a note with your street address.
Jan Czekajewski
e-mail : janczek@aol.com



From owner-biophysics@net.bio.net Mon Aug 04 23:00:00 1997
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From: Petr Kuzmic <pkuzmic@biokin.com>
Newsgroups: bionet.software,bionet.biophysics,bionet.metabolic-reg
Subject: Thrombin/Hirudin: Rate constants determined by DYNAFIT
Date: Tue, 05 Aug 1997 02:28:36 -0500
Organization: BioKin Consulting
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Xref: biosci bionet.software:19274 bionet.biophysics:3435 bionet.metabolic-reg:1545

This is a message to all users of the freeware program DYNAFIT
--------------------------------------------------------------
August 4, 1997

THROMBIN TUTORIAL - COMPETITIVE BINDING KINETICS

   A new online tutorial was added: Determination of rate constants  for
the simultaneous, competitive binding of thrombin and its chemical
mutant (dehydrothrombin) to hirudin.  Everyone is encouraged to compare
the approach described on the BioKin website [1] with the original paper
from Scheraga's laboratory at Cornell [2].

   Since I am planning to submit the re-analysis of the thrombin data as
a journal article, any comments, criticisms, and suggestions for
improvements are welcome.  Please take a look at the original report [1]
and observe the spectacular complexity of the algebraic approach: 97
equations and three appendices in ref. [1], compared with the DYNAFIT
[2] formalism:

[mechanism]

   Enzyme + Ligand <===> Complex-1  :   k1   k2
   Mutant + Ligand <===> Complex-2  :   k3   k4

REFERENCES

[1] Wedemeyer et al. (1997) Anal. Biochem. 248, 130-140.
[2] http://www.biokin.com/dynafit/tutorial/thrompap.shtml

--------------------------------------------------------------
Petr Kuzmic Ph.D. * BioKin Ltd. * Madison, WI 53708-8336 (USA)
(pkuzmic@biokin.com) [http://www.biokin.com] 608.256.1269 fax



From owner-biophysics@net.bio.net Mon Aug 04 23:00:00 1997
Path: biosci!PIAFFE.USASK.CA!kendalle
From: kendalle@PIAFFE.USASK.CA
Newsgroups: bionet.biophysics
Subject: Re: thermodynamic texts
Date: 5 Aug 1997 08:26:38 -0700
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Intermediate Physics for Medicine and Biology
Russell K. Hobbie
John Wiley and Sons.
Miriam ,

I have found the above text very useful in teaching resident radiologists and other biologists.

ed kendall

> From heynen@sciborg.uwaterloo.ca Thu Jul 31 15:25:47 1997
> Return-Path: <BIOSCI-REQUEST@net.bio.net@piaffe.usask.ca>
> To: biophys@net.bio.net
> From: heynen@sciborg.uwaterloo.ca (Miriam Heynen)
> Subject: thermodynamic texts
> Sender: news@watserv3.uwaterloo.ca
> Nntp-Posting-Host: sciborg.uwaterloo.ca
> Date: Thu, 31 Jul 1997 15:52:29 GMT
> 
> 
> Can anyone recommend a text or review articles that explain the equations
> and concepts of thermodynamics as applied to biology?  I have had one year
> of physics and math so something descriptive rather than mathematical is
> helpful maybe even necessary.
> 
> thanks, miriam
> heynen@sciborg.uwaterloo.ca
> 
> -- 
> bye, miriam
> 
> Miriam Heynen
> heynen@sciborg.uwaterloo.ca
> 
> 

From owner-biophysics@net.bio.net Tue Aug 05 23:00:00 1997
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From: (Autor Casi) junko*SPAM@cyberspace.*BLOCK.org
Newsgroups: bionet.cellbiol,bionet.biophysics,bionet.general,bionet.microbiology
Subject: Cell Death and CO gas absorption questions
Date: Wed, 06 Aug 1997 15:45:48 GMT
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Xref: biosci bionet.cellbiol:7888 bionet.biophysics:3437 bionet.general:27711 bionet.microbiology:10682


Can someone answer the following questions (thanks ahead):

1) Do skin cells absorb Carbon Monoxide (CO) gas while viable (living)?

2) Do skin cells exude/push out CO gas while living?  (I assume so)

3) Upon dying, will skin cells start absorbing heavy amounts of CO gas from
their immediate environment (assuming CO gas is present)?

4) Does cell function (organelle, enzymatic activity) stop fairly soon upon
cell death?  What activities might linger?

5) What factors influence the RATE of CO gas absorption in a "dead" skin cell?
(CO outside concentration, membrane permeability...)

6) What is the best way to measure CO gas concentration absorbed by skin
cells?

7) What enzymes in skin cells are primarily involved in CO
breakdown/exuding/rejection?

Thanks much to any and all responses.

--AC
Remove SPAM BLOCK in e-mail to reply.
I will try to check newgroups.


-----------------------------------------------------------------
Things are more like they are now, than they've ever been before.


From owner-biophysics@net.bio.net Tue Aug 05 23:00:00 1997
From: Anthonie Muller <awjm@holyrood.ed.ac.uk>
Newsgroups: bionet.biophysics
Subject: Re: thermodynamic texts
Date: Wed, 6 Aug 1997 17:52:52 +0100
Organization: Edinburgh University
Lines: 27
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To: Miriam Heynen <heynen@sciborg.uwaterloo.ca>
In-Reply-To: <EE6xFH.Ey8@watserv3.uwaterloo.ca>
Path: biosci!agate!hammer.uoregon.edu!vixen.cso.uiuc.edu!howland.erols.net!cpk-news-hub1.bbnplanet.com!news.bbnplanet.com!news-feed.inet.tele.dk!easynet-uk!news.mite.net!uknet!newsfeed.ed.ac.uk!holyrood.ed.ac.uk!awjm

On Thu, 31 Jul 1997, Miriam Heynen wrote:

> Can anyone recommend a text or review articles that explain the equations
> and concepts of thermodynamics as applied to biology?  I have had one year
> of physics and math so something descriptive rather than mathematical is
> helpful maybe even necessary.
> 
> Miriam Heynen


Hi Miriam

On my thermosynthesis home page I give a short introduction to
thermodynamics from basic principles. In contrast to most contemporary
treatments for life scientists I define entropy as the integral of dQ/T -
some may consider this as an old fashioned approach, but IMHO that still
is the best way to do it. The mathematics is simple - just read the part 
on entropy a few times until you are sure you have grasped it. 

Thermodynamics is fun!


Anthonie Muller

The Thermosynthesis Home Page
http://www.ed.ac.uk/~awjm


From owner-biophysics@net.bio.net Tue Aug 05 23:00:00 1997
Path: biosci!IFQSC.SC.USP.BR!luciano
From: luciano@IFQSC.SC.USP.BR (Luciano Costa)
Newsgroups: bionet.biophysics
Subject: NEW Call for Papers = Special Issue Biomedical Signal Processing
Date: 6 Aug 1997 10:17:43 -0700
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5th July 97

Dear Friends,

Please note that the recently disseminated version of the CFP
(Special Issue on Biomedical Signal Processing) was INCOMPLETE.
Please find enclosed the COMPLETE version of the CFP.

Yours ever, Luciano

=============================================================================

                             CALL FOR PAPERS

                APPLIED SIGNAL PROCESSING - Springer-Verlag

               SPECIAL ISSUE ON BIOMEDICAL SIGNAL PROCESSING


-------------------------------------------------------------------------

Guest Editors:

Luciano da F. Costa,
Cybernetic Vision Research Group,
DFI-IFSC, University of Sao Paulo
Caixa Postal 369,
Sao Carlos, SP
13560-970
Brazil
Tel: +55 162 74 9199
Fax: +55 162 71 3616
E-Mail: luciano@ifqsc.sc.usp.br

William Sandham,
Department of Electronic and Electrical Engineering,
University of Strathclyde
Glasgow G1 1XW
Scotland
Tel: +44 141 548 2406
Fax: +44 141 552 2487
E-Mail: w.sandham@eee.strath.ac.uk

-------------------------------------------------------------------------

The last two decades of scientific development have been characterised
by major advances in biomedical technology. Genetic and biomolecular
engineering have progressed from science fiction to reality, and
diagnostic techniques such as CT, MRI, PET and SPECT, have evolved from
basic research to widespread use in hospitals. Major breakthroughs have
been made in the neural sciences, which have led to a better
understanding
of biological neural structures, and the engineering of more
powerful and versatile artificial neural networks and models.

As we enter the 21st century, these technologies are destined to
reach a level of development which will redefine many concepts
and alter the human perspective in an unprecedented way.
Many of these developments have been made possible through major
advances in theoretical and applied signal processing.
Deterministic methods for analysis and synthesis, such as those
based on the short-time Fourier transform and wavelets, have now reached

maturation, and excellent progress has been made using
statisticalmethods
such as Markov random fields, regularization theory,
and Kalman filtering, for noise suppression, signal enhancement and
optimisation.

The advent of new biomedical devices, sensors and families of generic
and dedicated processors have also proven to be essential enabling
technologies for practical applications of such increasingly complex
techniques.

This Special Issue will review the current status of
biomedical signal processing, and address future techniques
and applications.  Submissions should either provide a comprehensive
perspective on topics of special relevance (see list below) or
report novel advances in the theory and application of methods and
architectures for biomedical signal processing.

Papers are invited, but are not limited, to the topics listed below:

Biomedical Topics:
        * ECGs and EEGs
        * Event related (evoked) potentials
        * Morphometry        * DNA analysis
        * Medical imaging
        * Tomography and optical imaging
        * Microscopy
        * Biomagnetism
        * Echocardiography
        * Radiology and Radiotherapy
        * Diagnostic ultrasound
        * Biophysics
        * Biosensors

Signal Processing Topics:
        * Medical informatics
        * Mathematical modeling and simulation
        * Measurement and medical instrumentation
        * Image processing, visualization and computer vision
        * Computational neuroscience
        * Artificial neural networks
        * Chaos and fractals
        * Wavelets and time-frequency analysis
        * Higher-order statistics
        * Non-linear analysis        * Adaptive techniques

Paper Submission:
Prospective authors should prepare their manuscripts in the accepted
ASP format, and send 4 copies to Luciano Costa at the above address.
Papers will be reviewed by senior researchers from industry and
academia.

Schedule:
Paper Submission Deadline               28 February 1998
Notification of Acceptance/Rejection    30 May 1998
Final Submission Deadline               27 August 1998

-----------------------------------------------------------------------

PLEASE FEEL FREE TO REQUEST THE INSTRUCTIONS FOR AUTHORS TO:

                             Luciano Costa,  luciano@ifqsc.sc.usp.br

========================================================================






From owner-biophysics@net.bio.net Thu Aug 07 23:00:00 1997
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From: Jon B Applequist <jba@iastate.edu>
Newsgroups: bionet.biophysics
Subject: Re: Donnan potential < > PENTCHO VALEV
Date: Sat, 02 Aug 1997 19:52:08 -0500
Organization: Iowa State University, Ames, Iowa, USA
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RUMYM@BGEARN.ACAD.BG wrote:
> 
>  Lars Thompsen wrote:
>  When one is measuring a potential difference then it is done by using a   <
> apparatus with a high resistance to ensure that no current is passing      <
> through the measuring device, which eventually would obscure the           <
> measurement.  As the resistance of the voltmeter is many times that of the <
> resistance found between any points in the water (how long did you want to <
> make the tube) then I am certain that would still be able to measure the   <
> voltage difference. As you are measuring on a equilibrium sitiaution I cant<
> see any errors that will distort your measurement even when you are moving <
> the electrodes away from the membrane.                                     <
>                                                                            <
> However, it is a totally different case if you want to voltage clamp the   <
> membrane (for whatever reason) then you would have to consider where you   <
> should put your electrodes, because that  would influence the potential    <
> across the membrane. If you e.g. moved your current passing electrodes away<
> from the membrane then you would have to consider the voltage drop across  <
> the solution infront of the membrane.                                      <
>                                                                            <
> Please correct me if Im wrong                                              <
> 
> No I can't correct you - I am rather incompetent in electrochemistry. But I
> see the situation at the membrane as a local event - the potential at each
> side of the membrane is similar to Gui-Chapman potential - it decreases in
> magnitude with distance and eventually becomes zero. That is why I expect
> the potential difference between points symmetrical with respect to but
> distant from the membrane to be zero.
>    However some say that the zero on the left is different from that on the
> right, i.e. that the potential difference even between points infinitely
> distant from the membrane will be preserved.
>    This week I am going to make the experiment. However it will be rather
> primitive, so I would be happy to receive competent opinions: what should I
> expect: that the potential difference will be preserved away from the membrane
> or that it will become zero.
>    The answer to this question may have very serious thermodynamic implications
> 
> Pentcho
At equilibrium the potential throughout a conducting phase has to be
constant; otherwise, there would be currents flowing, which would not be
an equilibrium situation.  Therefore, the potential across the membrane
should not depend on the location of the electrodes within the phases.

From owner-biophysics@net.bio.net Thu Aug 07 23:00:00 1997
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From: <RUMYM@BGEARN.ACAD.BG>
Newsgroups: bionet.biophysics
Subject: Donnan potential < > PENTCHO VALEV
Date: 8 Aug 1997 09:02:09 +0100
Lines: 36
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Original-To: biophys@dl.ac.uk

In reply to Jon Applequist

Jon, I see no reason why, at equilibrium, the potential throughout a
conducting phase should be constant. Is Gui-Chapman potential constant?
   Still I find my original presentation of the problem too vague. Let
me reset it, by using a system much more "natural" and by singling out the
essential questions to be answered.


     I--------------------------I-----------------------------I

     I  c       Na+ A-      a  -I+  b    sacharose       d    I


     I--------------------------I-----------------------------I

   We have two compartments divided by a membrane permeable only to Na+
and water.  There is  Na+A- solution in the left-hand compartment (A- is
some big anion) and water plus sacharose in the right-hand one (the role
of sacharose is only to equalise the osmotic pressure).
   As some Na+ crosses the membrane, its right-hand side gets positively
charged and the left-hand one negatively. This means that, at equilibrium,
there will be an electrical potential difference between points symmetrical
with respect to and close to the membrane (a and b).
   This is universally accepted. However it is not at all clear whether this
potential difference will be preserved for points symmetrical with respect to
but distant from the membrane (c and d).  I believe not.
   Moreover, the following absurd conclusion seems unavoidable. In the
right-hand compartment, far from the membrane, the Na+ concentration obviously
approaches zero. This means that the Na+ chemical potential approaches
-infinity. Therefore, in order that the Na+ electrochemical potential remains
constant (as thermodynamics requires), the electrical potential must approach
+infinity. There can be nothing more absurd than that, and I see no solution
in terms of thermodynamics.

Pentcho

From owner-biophysics@net.bio.net Thu Aug 07 23:00:00 1997
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From: tivol@news.wadsworth.org (William Tivol)
Newsgroups: bionet.biophysics
Subject: Re: Donnan potential < > PENTCHO VALEV
Date: 8 Aug 1997 13:59:44 GMT
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RUMYM@BGEARN.ACAD.BG wrote:

:      I--------------------------I-----------------------------I

:      I  c       Na+ A-      a  -I+  b    sacharose       d    I


:      I--------------------------I-----------------------------I

:    We have two compartments divided by a membrane permeable only to Na+
: and water.  There is  Na+A- solution in the left-hand compartment (A- is
: some big anion) and water plus sacharose in the right-hand one (the role
: of sacharose is only to equalise the osmotic pressure).
:    As some Na+ crosses the membrane, its right-hand side gets positively
: charged and the left-hand one negatively. This means that, at equilibrium,
: there will be an electrical potential difference between points symmetrical
: with respect to and close to the membrane (a and b).
:    This is universally accepted. However it is not at all clear whether this
: potential difference will be preserved for points symmetrical with respect to
: but distant from the membrane (c and d).  I believe not.

	I see no reason to think that such a potential difference is not
present at points c & d.  At equilibrium, there will be no potential
difference between points a & c and between points b & d (assuming that
there is a conducting pathway betweeen these points.

:    Moreover, the following absurd conclusion seems unavoidable. In the
: right-hand compartment, far from the membrane, the Na+ concentration obviously
: approaches zero.

	Not at equilibrium.  The Na+ concentration at point d must be equal
to that at point b.  Thermodynamics, then, requires constant electrical and
chemical potentials at points b & d.  There is no absurdity.
				Yours,
				Bill Tivol

From owner-biophysics@net.bio.net Thu Aug 07 23:00:00 1997
Path: biosci!daresbury!not-for-mail
From: <RUMYM@BGEARN.ACAD.BG>
Newsgroups: bionet.biophysics
Subject: Donnan potential < > PENTCHO VALEV
Date: 8 Aug 1997 17:53:52 +0100
Lines: 48
Sender: lpddist@mserv1.dl.ac.uk
Distribution: bionet
Message-ID: <5sfiv0$j8b@mserv1.dl.ac.uk>
Original-To: biophys@dl.ac.uk

Bill Tivol wrote:                                                   <
RUMYM@BGEARN.ACAD.BG wrote:                                         <
                                                                    <
:      I--------------------------I-----------------------------I   <
                                                                    <
:      I  c       Na+ A-      a  -I+  b    sacharose       d    I   <
                                                                    <
                                                                    <
:      I--------------------------I-----------------------------I   <
                                                                    <
:    We have two compartments divided by a membrane permeable only to Na+   <
: and water.  There is  Na+A- solution in the left-hand compartment (A- is  <
: some big anion) and water plus sacharose in the right-hand one (the role  <
: of sacharose is only to equalise the osmotic pressure).                   <
:    As some Na+ crosses the membrane, its right-hand side gets positively  <
: charged and the left-hand one negatively. This means that, at equilibrium,<
: there will be an electrical potential difference between points symmetrical<
: with respect to and close to the membrane (a and b).                       <
:    This is universally accepted. However it is not at all clear whether this<
: potential difference will be preserved for points symmetrical with respect to
: but distant from the membrane (c and d).  I believe not.                  <
                                                                            <
    I see no reason to think that such a potential difference is not           <
present at points c & d.  At equilibrium, there will be no potential        <
difference between points a & c and between points b & d (assuming that     <
there is a conducting pathway betweeen these points.                        <

Bill, if your claim at the end of your posting (see below) was correct, the
above would be also correct.

:    Moreover, the following absurd conclusion seems unavoidable. In the   <
: right-hand compartment, far from the membrane, the Na+ concentration obviously
: approaches zero.                                                         <
                                                                           <
    Not at equilibrium.  The Na+ concentration at point d must be equal       <
to that at point b.  Thermodynamics, then, requires constant electrical and<
chemical potentials at points b & d.  There is no absurdity.               <

How can you claim that the Na+ concentration at point d is equal to that at
point b? The same discussion is carried out in the btk-mca group, and
everybody agree that, in the right-hand compartment, Na+ can be found at
a distance not more than 1 nanometer from the membrane.
   Maybe you mean that the Na+ concentration is zero at both b and d? What
would be the electrical potential at these points then (so that the
electrochemical potential at these points is the same as in the whole
system)?

Pentcho

From owner-biophysics@net.bio.net Thu Aug 07 23:00:00 1997
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From: Malcolm Young <m.p.young@ncl.ac.uk>
Newsgroups: bionet.biophysics
Subject: NEUROPHYSIOLOGY JOB
Date: Fri, 08 Aug 1997 16:27:49 +0200
Organization: University of Newcastle upon Tyne
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NEURAL SYSTEMS GROUP, NEWCASTLE UNIVERSITY.
 
We have a postdoctoral position from October 97 for a visual
neurophysiologist. The project will examine the possible role of
neuronal synchrony in visual feature binding.

The post is funded at the Wellcome Trust's Level 2. Ideally, we would
like to find someone with good experience in visual neurophysiology;
some experience in visual psychophysics; experience in computational
analysis (e.g. using information theory); and experience in graphics
programming, most usefully with the VSG system. But this is a tall
order, and people with subsets of these skills should certainly apply
if interested.
 
The project is empirical -  the data and experimental controls
will tell us what to conclude about this controversial issue - and so
an applicant's degree of enthusiasm or scepticism for the
binding-by-synchrony theory is not important. Motivation to address
the uncertainties in visual feature integration is much more important.
 
Please will interested neurophysiologists contact Malcolm Young, Martin
Tovee or Jack Scannell at:
 
malcolm@flash.ncl.ac.uk
m.j.tovee@ncl.ac.uk
j.w.scannell@ncl.ac.uk
 
Malcolm Young
Neural Systems Group
Faculty of Medicine
Newcastle upon Tyne
NE1 &RU
U.K.

From owner-biophysics@net.bio.net Thu Aug 07 23:00:00 1997
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From: Petr Kuzmic <pkuzmic@biokin.com>
Newsgroups: bionet.biophysics
Subject: Program DynaFit: BioInformer & MEDLINE links
Date: Fri, 08 Aug 1997 09:29:56 -0500
Organization: BioKin Consulting
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DYNAFIT Featured in BIOINFORMER
--------------------------------------- 
Program DYNAFIT [P. Kuzmic (1996) Anal. Biochem. 237, 260-273]
for the statistical analysis of biochemical data is featured 
in the Summer '97 issue of BIOINFORMER - A quarterly 
publication of the European Bioinformatics Institute:

http://bioinformer.ebi.ac.uk/newsletter/
http://bioinformer.ebi.ac.uk/newsletter/archives/2/Dynafit.html

MEDLINE Link
------------
MEDLINE (National Library of Medicine) contains an abstract
referencing the original publication of DYNAFIT.  To view the
abstract, link your browser to

http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8660575&form=6&db=m&Dopt=r

_____________________________________________________________
Petr Kuzmic Ph.D. * BioKin Ltd. * Madison, WI 53708-8336, USA
pkuzmic@biokin.com * http://www.biokin.com * 608.256.1269 fax

From owner-biophysics@net.bio.net Sun Aug 10 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.apfel.de!chico.franken.de!news-nue1.dfn.de!wuff.mayn.de!fu-berlin.de!news.th-darmstadt.de!News.Uni-Marburg.DE!not-for-mail
From: JaoHan <yao@mailer.uni-marburg.de>
Newsgroups: bionet.biophysics
Subject: (no subject)
Date: 10 Aug 1997 09:56:34 GMT
Organization: HRZ Uni Marburg
Lines: 36
Message-ID: <33ED927B.12F5@mailer.uni-marburg.de>
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Postdoctoral Research Fellowship
in Molecular Biology



The project is funded by the TMR (Training and Mobility of Researchers)
and therefore addresses to young scientists who are members of countries
of the European Union. It involves the molecular analysis of
Bradyrhizobium japonicum signal peptidases and their roles in the
establishment and maintenance of symbiotic interactions with soybeans
and other host plants. The main goal of the project will be to analyze
the function of several newly identified genes of B. japonicum and to
study the influence of bacterial mutations on the host plant.

Applicants should have good knowledges in molecular genetics, gene
expression techniques, protein biochemistry and immunology.

Salary (tax free grant) will be up to DM 36,000.- per annum, and the
post is available immedeately for a period of two years.


Informal enquiries may be made to Dr Peter Müller

	Fax.: 0049 6421 28 8997
	Tel.: 0049 6421 28 2072
	e-mail: muellerp@nws.biologie.uni-marburg.de


Further information and details of how to apply may be obtained from 

	Prof. Dr. D. Werner
	Philipps University of Marburg
	Dept. of Biology/Botany
	Karl-von-Frisch-Straße
	35032 Marburg
	Germany

From owner-biophysics@net.bio.net Sun Aug 10 23:00:00 1997
Path: biosci!agate!newsfeed.kornet.nm.kr!howland.erols.net!EU.net!uknet!lyra.csx.cam.ac.uk!not-for-mail
From: Tom Chou <tc208@damtp.cam.ac.uk>
Newsgroups: bionet.biophysics
Subject: Latex .sty file for BioPhys J?
Date: Mon, 11 Aug 1997 02:09:54 +0100
Organization: DAMTP, University of Cambridge, UK.
Lines: 15
Message-ID: <33EE6662.167E@damtp.cam.ac.uk>
NNTP-Posting-Host: decant.amtp.cam.ac.uk
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Hi,

Does anyone have a latex .sty or .cls file
for preparing Biophys. J. manuscripts?

Or, can anyone tell me how to convert the 
revtex references (numerically sequenced)
to alphabetical by author?


Cheers,

Tom 

tc208@damtp.cam.ac.uk

From owner-biophysics@net.bio.net Sun Aug 10 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.apfel.de!chico.franken.de!news-nue1.dfn.de!wuff.mayn.de!fu-berlin.de!news.th-darmstadt.de!News.Uni-Marburg.DE!not-for-mail
From: JaoHan <yao@mailer.uni-marburg.de>
Newsgroups: bionet.biophysics
Subject: Ph.D.
Date: 10 Aug 1997 09:34:28 GMT
Organization: HRZ Uni Marburg
Lines: 36
Message-ID: <33ED8D4D.340E@mailer.uni-marburg.de>
Reply-To: yao@maier.uni-marburg.de
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Postdoctoral Research Fellowship
in Molecular Biology



The project is funded by the TMR (Training and Mobility of Researchers)
and therefore addresses to young scientists who are members of countries
of the European Union. It involves the molecular analysis of
Bradyrhizobium japonicum signal peptidases and their roles in the
establishment and maintenance of symbiotic interactions with soybeans
and other host plants. The main goal of the project will be to analyze
the function of several newly identified genes of B. japonicum and to
study the influence of bacterial mutations on the host plant.

Applicants should have good knowledges in molecular genetics, gene
expression techniques, protein biochemistry and immunology.

Salary (tax free grant) will be up to DM 36,000.- per annum, and the
post is available immedeately for a period of two years.


Informal enquiries may be made to Dr Peter Müller

	Fax.: 0049 6421 28 8997
	Tel.: 0049 6421 28 2072
	e-mail: muellerp@nws.biologie.uni-marburg.de


Further information and details of how to apply may be obtained from 

	Prof. Dr. D. Werner
	Philipps University of Marburg
	Dept. of Biology/Botany
	Karl-von-Frisch-Straße
	35032 Marburg
	Germany

From owner-biophysics@net.bio.net Mon Aug 11 23:00:00 1997
Newsgroups: bionet.biophysics
Path: biosci!bcm.tmc.edu!news.msfc.nasa.gov!europa.clark.net!205.252.116.205!howland.erols.net!vixen.cso.uiuc.edu!uchinews!news
From: "Bnlent" <XB@XB.net>
Subject: Acdemic or Indusrial position
X-Nntp-Posting-Host: ntcs-ip142.uchicago.edu
Message-ID: <01bca6d2$25029340$8f128780@computer.uchicago.edu>
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Reply-To: "Bnlent" <bnlent@geocities.com>
Organization: N/A
X-Newsreader: Microsoft Internet News 4.70.1161
Date: Tue, 12 Aug 1997 03:40:53 GMT
Lines: 24

Academic or Industrial position 

Cell physiology

My main interest in this area is the mechanism of signal transduction; Ca2+
entry regulation; characterization of ion transporting systems; interaction
between NO, cGMP, cAMP and IP3 signaling pathways; mechanism of membrane
channels and gap junction function and coupling to cell signaling pathways.
I have experience in working with different types of mammalian cells
(Myocytes, Skeletal muscle fibers, cell lines, Red Blood Cells, Neurons.).
I have strong background in fluorescent microscopy (Calcium, pH, and
membrane potential-sensitive dyes), Ca2+ imaging; patch-clamp
(cell-attached, whole-cell, double whole patch clamp and double perforated
patch)  on single cell and cell pairs, micro-injection of fluorescent dyes.
I also have experience in setting up an electrophysiology laboratory.
I am very flexible and eager to learn more techniques and methods. 
If interested, I will be happy to forward my CV along with other
information.

My E-mail is: bnlent@geocities.com

Thank you for your time and consideration.



From owner-biophysics@net.bio.net Mon Aug 11 23:00:00 1997
Path: biosci!news.Stanford.EDU!su-news-hub1.bbnplanet.com!news.bbnplanet.com!iagnet.net!howland.erols.net!infeed1.internetmci.com!newsfeed.internetmci.com!news.webspan.net!usenet
From: Olympicbks@aol.com (Harvey Abrams)
Newsgroups: bionet.biophysics
Subject: Catalog 18 - Physics books
Date: Tue, 12 Aug 1997 01:39:07 -0500
Organization: Harvey Abrams-BOOKS
Lines: 23
Message-ID: <Olympicbks-1208970139080001@a1-p04.sc.tioga.net>
NNTP-Posting-Host: a1-p04.sc.tioga.net
X-Report-Abuse-To: abuse@mail.webspan.net
NNTP-Posting-Date: 12 Aug 1997 01:37:36 EDT

In preparation - CATALOG 18 - Physics.

A library froma retired professor, 850 or so books and 2700 journals. To
be sold as a complete collection or as individual lots.

CATALOG 18 - to be available in September 1997.
Subscription cost: $10.00, postpaid.

Credit of $10.00 available on the buyer's invoice when purchases from the
catalog are over $100.00.

Books priced from $10.00 to $45.00.

Subscriptions to:
Harvey Abrams - BOOKS
PO Box 732
State College, PA USA 16804

fax: (814) 237-8332
email: Olympicbks@aol.com

-- 
Specializing in the Olympic Games, History of Sport & Physical Education, Fencing, Wrestling, Track & Field (Athletics) and all sports subjects; World's Fairs & Expositions (1847 - 1939). Catalogs available by subscription. Consignments accepted. Auctions. Appraisals. Web site: http://www.tioga.net/~olympic/

From owner-biophysics@net.bio.net Wed Aug 13 23:00:00 1997
Path: biosci!daresbury!lyra.csx.cam.ac.uk!hgmp.mrc.ac.uk!not-for-mail
From: David Starks-Browning <starksb@ebi.ac.uk>
Newsgroups: bionet.biophysics
Subject: Parallel Programming Course at EMBL-Heidelberg
Date: 14 Aug 1997 17:34:41 +0100
Organization: EBI - European Bioinformatics Institute
Lines: 58
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		     [please post and distribute]

The Supercomputing Resource for Molecular Biology (SRMB), located at
the European Molecular Biology Laboratory in Heidelberg, Germany, is
offering training courses in

	 Parallel Programming and High Performance Computing

to European researchers in molecular biology.  The next course will
be held 31 August - 4 September 1997.

The course is an intensive and comprehensive introduction to parallel
programming and high performance computing for European molecular
biologists.  Topics include:

     Heterogeneous distributed computing with PVM 

     Message passing programming with MPI 

     Data parallel programming with Fortran90/HPF 

     Methodologies for designing parallel algorithms 

     Performance modeling and scalability analysis 

     Optimization for modern microprocessors 

     Shared memory programming and parallelizing compilers 

     Case studies from parallel applications in molecular biology 

There is considerable emphasis on hands-on experience through
practical sessions.  In particular, participants will write and
execute their own parallel programs in PVM, MPI and Fortran90/HPF.

The course is open to European researchers at the advanced
post-graduate level who have research interests in molecular biology,
including sequence analysis, image processing, structure refinement,
protein design and molecular dynamics.  Participants from EU countries
will be supported by an EU HCM/ALSF grant.  Residents of other EMBL
member countries will be supported by funds from EMBL. Participants
receive travel, accommodation and a subsistence allowance during their
visit, as well as access to the computational facilities of the
Laboratory.

If you wish to attend you should fill out an online application form
AS SOON AS POSSIBLE.  Further information, with links to a detailed
agenda and application forms, can be found at:

     <http://www.embl-heidelberg.de/Services/srmb/pphpc_course/>

=========================================================================
David Starks-Browning                         | starksb@ebi.ac.uk
Technology Transfer Node Manager              !
European Bioinformatics Institute             !
Wellcome Trust Genome Campus                  ! tel: +44(0)1223-49 46 16
Hinxton, Cambridge CB10 1SD, UK               ! fax: +44(0)1223-49 44 68
=========================================================================

From owner-biophysics@net.bio.net Wed Aug 13 23:00:00 1997
Path: biosci!HAVERFORD.EDU!jdepaula
From: jdepaula@HAVERFORD.EDU (Julio de Paula)
Newsgroups: bionet.biophysics
Subject: liquid scintillation spectrometer
Date: 14 Aug 1997 12:47:04 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 22
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <l03110700b0191d865efe@[165.82.15.156]>
NNTP-Posting-Host: net.bio.net


We no longer need our Packard Tri-Carb Liquid Scintillation Spectrometer
(and associated teletype; yes, teletype).  It worked great last time I used
it for an undergraduate lab experiment (in 1990).  I have not fired it up
since.  If anyone is interested, please let me know; I will accept any
reasonable offer.  If anyone knows of a company who may be interested in
taking it off our hands, please let me know as well.

Thanks,

Julio.


Julio C. de Paula
Associate Professor of Chemistry
Haverford College
Haverford, PA 19041
phone:  610-896-1217
fax:    610-896-4904
email:  jdepaula@haverford.edu



From owner-biophysics@net.bio.net Thu Aug 14 23:00:00 1997
Path: biosci!agate!howland.erols.net!EU.net!news0.Belgium.EU.net!Belgium.EU.net!chaos.kulnet.kuleuven.ac.be!usenet
From: Guy Droogmans <guy.droogmans@med.kuleuven.ac.be>
Newsgroups: bionet.biophysics
Subject: WinASCD:  a program to analyze single channel and whole-cell pClamp current data
Date: Fri, 15 Aug 1997 11:17:39 +0200
Organization: K.U.Leuven
Lines: 34
Message-ID: <33F41EB3.7EC6@med.kuleuven.ac.be>
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WinASCD is a program to analyze single channel and whole-cell pClamp
data (Clampex, Fetchex, AxoTape).
It is a 32-bit (WIn95/NT) updated version of an original DOS program
that I started writing more than 10 years ago.
It includes the following main features:
1. a data correction module for
        baseline restoration (drift correction)
        background subtraction (correction for leak and capacitative
current)
2. a module for calculating average and peak currents
        ensemble averaged current
        avg current for continuous data
        avg and peak current for triggered data
3. a module to construct linear combinations of records belonging to the
same or 
        different files
4. a module to fit sum of exponentials or a kinetic model to indivudual
current traces, 
        ensemble averaged currents and composed records
5. a module for the Analysis of Single Channel Data, including
    Amplitude histogram construction and fit with Gauss peaks
    Kinetic Analysis: idealization, dwell time histograms, first
latencies, burst analysis,
                                analysis of the number of events
6. a module for the analysis of current fluctuations, including current
variance analysis 
        and FFT.

Each window (graphical or text) can be printed (not a screen dump) or
saved as a TAB delimited ASCII file for import in e.g. a presentation
software package.

To get a trial version of this software contact me by e-mail at 
Guy.Droogmans@med.kuleuven.ac.be

From owner-biophysics@net.bio.net Thu Aug 14 23:00:00 1997
Path: biosci!agate!newsfeed.kornet.nm.kr!news.maxwell.syr.edu!demos!news1.relcom.ru!news.nsk.su!mpeks.tomsk.su!tsu.tomsk.su!usenet
From: Sergey Scharubin <sch@biobase.tsu.tomsk.su>
Newsgroups: bionet.biophysics
Subject: Re: Help !!!
Date: Fri, 15 Aug 1997 17:50:53 +0700
Organization: Rein BB
Lines: 7
Message-ID: <33F4348D.7419@biobase.tsu.tomsk.su>
Reply-To: sch@biobase.tsu.tomsk.su
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Hi All !!!
Give me article. Please.
Umeda K., Shiota S., Futai M. Enhibitory effect of Li om cell growth
andpyruwate kinase activity of Escherichia coli. // J. Bacteriol -19484
-160 N12, 812 - 814
Sergey
sch@biobase.tsu.tomsk.su

From owner-biophysics@net.bio.net Thu Aug 14 23:00:00 1997
Path: biosci!daresbury!uninett.no!sn.no!www.nntp.primenet.com!globalcenter1!news.primenet.com!nntp.primenet.com!news.maxwell.syr.edu!news-peer.sprintlink.net!news-pull.sprintlink.net!news-in-east.sprintlink.net!news.sprintlink.net!Sprint!128.228.4.60!news.cuny.edu!nntp.upenn.edu!axe1.med.upenn.edu!axelsen
From: axelsen@axe1.med.upenn.edu (Paul H Axelsen)
Newsgroups: bionet.biophysics
Subject: POSTDOCTORAL POSITIONS: Molecular Recognition and Membrane Biophysics
Date: 15 Aug 1997 22:53:04 GMT
Organization: University of Pennsylvania
Lines: 31
Message-ID: <5t2mkg$nbk$3@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

Projects involve the use of novel spectroscopic techniques (infrared and UV)
and mass spectrometry to study the behavior of antibiotics, fusogenic peptides,
and blood coagulation proteins on lipid membranes with a view towards rational
drug design.  The laboratory is stably funded and the positions are available 
immediately.  Applicants MUST be available for interview prior to appointment.
Persons with a talent for mastering sophisticated new technology, and seeking 
to work on important biomedical problems, should inquire by email to 

                      axe@pharm.med.upenn.edu
or

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)
http://axe2.med.upenn.edu (www)


--

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

From owner-biophysics@net.bio.net Fri Aug 15 23:00:00 1997
Path: biosci!agate!hammer.uoregon.edu!vixen.cso.uiuc.edu!howland.erols.net!infeed1.internetmci.com!newsfeed.internetmci.com!152.163.199.19!portc03.blue.aol.com!newstf02.news.aol.com!audrey01.news.aol.com!not-for-mail
From: huntpharm@aol.com (Huntpharm)
Newsgroups: bionet.biophysics
Subject: US-MD-JOB OPPORTUNITY IN POLYMERS
Date: 16 Aug 1997 20:37:12 GMT
Lines: 11
Message-ID: <19970816203701.QAA13623@ladder01.news.aol.com>
NNTP-Posting-Host: ladder01.news.aol.com
X-Admin: news@aol.com
Organization: AOL http://www.aol.com

I am looking for a Associate Scientist to perform synthesis on
biodegradable polymers. The candidate will have 1+ years experience with a
pharmaceutical or bio-tech company.   You should possess a B.S. or
M.S.degree in Chemistry, Chemical Engineering or medical sciences. 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 vactation 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.com or sis@diedremoire.com


From owner-biophysics@net.bio.net Fri Aug 15 23:00:00 1997
Path: biosci!news.Stanford.EDU!su-news-hub1.bbnplanet.com!cpk-news-hub1.bbnplanet.com!news.bbnplanet.com!infeed1.internetmci.com!newsfeed.internetmci.com!152.163.199.19!portc03.blue.aol.com!newstf02.news.aol.com!newstf01.news.aol.com!audrey02.news.aol.com!not-for-mail
From: huntpharm@aol.com (Huntpharm)
Newsgroups: bionet.biophysics
Subject: US-NC-HEAD OF STRUCTURAL CHEMISTRY
Date: 16 Aug 1997 18:57:43 GMT
Lines: 13
Message-ID: <19970816185700.OAA14586@ladder02.news.aol.com>
NNTP-Posting-Host: ladder02.news.aol.com
X-Admin: news@aol.com
Organization: AOL http://www.aol.com

I am looking for a PhD Scientist to be the Head of the Department of
Structural Chemistry. The candidate will have a strong background in
either X-Ray Crystallography or Computational Chemistry .  As the person
in this visionary role, you will be responsible for leading a group of
sixteen scientists and growing.  You should possess a PhD with 5+ years
experience and strong publication record. We are a leading pharmaceutical
company with research facilities in North Carolina and can provide
excellent benefits (health insurance, dental, and vision plan, bonus
program, paid vactation and more). Excellent compensation package. 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@diedremoire.com


From owner-biophysics@net.bio.net Fri Aug 15 23:00:00 1997
Path: biosci!news.Stanford.EDU!su-news-hub1.bbnplanet.com!cpk-news-hub1.bbnplanet.com!news.bbnplanet.com!howland.erols.net!csir.uni.net.za!und.uni.net.za!und.ac.za!newsadmin
From: "che" <pillayc@biochem.unp.ac.za>
Newsgroups: bionet.biophysics
Subject: redox buffers
Date: 16 Aug 1997 13:34:19 GMT
Organization: University of Natal, Pietermaritzburg
Lines: 18
Message-ID: <01bcaa49$1e975520$df80808f@bchm7.bch.unp.ac.za>
NNTP-Posting-Host: unpsun3.cc.unp.ac.za
X-Newsreader: Microsoft Internet News 4.70.1155
Cache-Post-Path: unpsun3.cc.unp.ac.za!unknown@bchm6.bchm.unp.ac.za

Hi everyone,

Does anyone out there have protocols/literature on how to make-up redox
buffers, i.e. buffers with a defined pH as well as reduction potential ? 
Ideally, this buffer system should be able to support a fairly wide range
of pH values and reduction potentials.


Thank you for taking the time to read this message.

Che Pillay
Dept. of Biochemistry
University of Natal
P/bag X 01
Scottsville
3209, 
South Africa
e-mail: Pillayc@biochem.unp.ac.za

From owner-biophysics@net.bio.net Sat Aug 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 Aug 1997 02:00:07 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 233
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199708170900.CAA08025@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 Sun Aug 17 23:00:00 1997
Path: biosci!agate!newsfeed.kornet.nm.kr!howland.erols.net!infeed1.internetmci.com!newsfeed.internetmci.com!203.146.0.24!news.loxinfo.co.th!NewsWatcher!user
From: connect@chmai.loxinfo.co.th (AJP)
Newsgroups: bionet.biophysics
Subject: Immortality 2 ***************************************************
Date: 18 Aug 1997 20:59:59 GMT
Organization: Loxley Information Company Thailand
Lines: 47
Message-ID: <connect-1808971358080001@208.147.7.94>
NNTP-Posting-Host: 208.147.7.94

I am pleased that,  already, there have been a number of responses to my
original posting on Immortality.  

(For future reference,  I will post the subject "Immortality" with a
number, so people can follow the postings through in the appropriate
order.)

With those responses I am getting questions and requests for further
details and information which is understandable given the somewhat vague
content of the posting.

I am also getting questions that would potentially require a great deal of
time and energy to answer properly (assuming I can answer all questions). 

For the above reason, my original intention to establish a central
location for this kind of International activity, postings, and further
research, is being justified by the obvious interest and response.

For those of you who have asked for more specific information,  
please be patient,  that time will come but only under the appropriate
conditions.

My approach, focus, and research on the subject of immortality, has
nothing to do with pills, electromagnetic fields, or any typicalform of
activity or product that, supposedly promotes or facilitates so-called
life extension.

The area I find myself in,  is so very delicate and sensative from many
points of view and perspectives, that I must be responsible and careful
with what is said and done. 

This is not just another opinion, it is a bio-physical fact. 

At this time,  I would like people to post their interest with the
appropriate groups or email me direct at .......
connect@chmai.loxinfo.co.th

If you post to the groups as well as direct, we can collectively pull
everyone interested in this subject out of the woodwork and centrally
connect them all.

Once an appropriate number of people have established the connection, I
will begin setting up the proposed Internet Based Center.


Kind Regards,
AJP.

From owner-biophysics@net.bio.net Sun Aug 17 23:00:00 1997
Path: biosci!agate!hammer.uoregon.edu!vixen.cso.uiuc.edu!howland.erols.net!cpk-news-hub1.bbnplanet.com!news.bbnplanet.com!baron.netcom.net.uk!netcom.net.uk!server3.netnews.ja.net!news.ox.ac.uk!andypmac.zoo.ox.ac.uk!user
From: enquiries@vei.co.uk
Newsgroups: bionet.biophysics
Subject: Bioinformatics Conference
Date: Mon, 18 Aug 1997 09:40:43 +0100
Organization: Virtual Environments International
Lines: 207
Message-ID: <enquiries-1808970940430001@andypmac.zoo.ox.ac.uk>
NNTP-Posting-Host: andypmac.zoo.ox.ac.uk


        Bioinformatics IEC-1 - FIRST INTERNET-EXTENDED BIOINFORMATICS CONFERENCE
        ************************************************************************
 

     The First Internet-Extended Bioinformatics conference will be held from 
Monday Nov 17 -> Friday Nov 28 1997 and will combine the use of a virtual 
conference and workshop (http://www.vei.co.uk/bioinfiec1/)followed by a
physical conference and workshop
in the Paragon hotel in London, UK.  The virtual conference and workshop will
run from Nov 17, the physical workshop will take place on Nov 26 and  the
physical conference on Nov 27-28.

     The focus of the conference is on the methods of bioinformatics  and
their application to current topical areas of research including genomics,
datamining, lead drug discovery, sequence retrieval, alignment and
modelling, molecular evolution, phylogenetic analysis, genetic variation,
functional analysis and visualisation. A special feature of the event will
be the use of Internet technology to enhance and extend the activities of
the event both in the
use and demonstration of methods and software and in the extension of the
physical event to include virtual activities before and during the
physical conference.
Bioinformatics has unique and significant activities in both the  private
and public sectors and the target audience for the physical conference will
be senior researchers and managers in both. The virtual facilities will
also extend the event to a broader international audience both to
corporate intranets and
to academic researchers in remote locations.

     The virtual conference will allow the presentation of virtual lectures,
papers and posters via the WWW, their discussion in a real-time virtual
conference centre and the demonstration of methods, software and tools.
The virtual workshop will allow registrants to participate in tutorials and
applications over the Internet in the ten days proceeding the physical 
conference which will host an all-day hands-on physical
workshop at an on-site bank of computers with an Internet conection.

     The physical conference will consist of lectures, panel discussions, 
an electronic poster session, and exhibitor stands.  The lectures will be 
broadcast live over the Internet using audio, live cameras and a  virtual
slide facility with questions and comments accepted live from virtual
participants.  

     Presentations for the virtual conference must be prepared in
Hypertext Markup 
Language (HTML) with figures in GIF or other Web-compatible formats so that 
participants can view the papers via the World Wide Web (The presentations
may also 
include enhancements such as 3D structures, VRML, Java, RealAudio,
Quicktime movies etc.) 
Powerpoint presentations will be used for the virtual presentation of
conference lectures. 
Aid and consultation is provided to participants who may address their
queries to the 
conference hot-line at bioinforg@vei.co.uk. Further details will be given
in the authors' 
guide accessible via http://www.vei.co.uk/bioinfiec1/.

     Conference sections by topic are: Molecular Evolution, Virology, 
Datamining; Lead Drug Discovery; Sequence retrieval, Alignment and Modelling;
Phylogenetic analysis; Genetic variation; Functional Analysis; Visualisation;
Population Analysis; Internet Databases & Information Retrieval;
Structural Biology;
HIV Modelling; Prions; and Applications in Cancer Research.

     During the virtual conference interaction, presentations and
discussions will take place 
via the Internet using a Java-based virtual conference centre, WWW-based
discussion 
forums and an electronic mailing list. Before the conference, a 
timetable for lectures and discussion sessions for each section will be posted. 

     The virtual and physical workshops will cover topics including search
engines,
biological resources on the WWW, bibliographic databases, sequence
retrieval and alignment,
structure generation and advanced modelling and visualization techniques.

     The Conference will feature a Virtual Exhibition where sponsors and
exhibitors will 
be able to describe the activities of their organization, or display their
products and 
services and interact with registrants. Potential sponsors and exhibitors
should contact the 
conference organisers at bioinforg@vei.co.uk.

DEADLINES AND DATES               

1) DO NOW - The Bioinformatics Conference mailing list

Conference-related news and announcements will be posted regularly 
to the mailing list (bioinf@vei.co.uk).  If you are receiving this
message from the bioinf list you are already subscribed. 

If you wish to subscribe to the bioinf list send the following
one line message to bioinf-request@vei.co.uk:

subscribe bioinf@vei.co.uk your_email@address 

To unsubscribe send the following message:

unsubscribe bioinf@vei.co.uk your_email@address 

2) Registration

If you intend to participate in Bioinformatics IEC-1 please use the
special registration 
form accessible via http://www.vei.co.uk/bioinfiec1/.  The electronic 
registration will be used to construct a registrant database for the 
conference which will generate the conference mailing list and handle 
assignment of userids and passwords.

Virtual Conference & Virtual Workshop: 75 pounds (125 dollars)
(88 pounds inc. VAT) 
"Combined" Physical & Virtual Conference: 540 pounds (900 dollars)
(635 pounds inc. VAT) 
"Combined" Academic fee (limited availability): 180 pounds (300 dollars)
(212 pounds inc. VAT) 
Additional Fee for Physical Workshop Attendance: 200 pounds (335 dollars)
(235 pounds inc. VAT)

In addition it is necessary to pay for registration via ordinary 
means: 

Registration payments can be accepted by credit card,
direct bank transfer, cheque or bank draft.

Payment Instructions:

a) Credit Card

We can currently accept Visa, Mastercard, Switch or JCB.

Please send your credit card type, number and expiration date
via 
a) regular mail to:
Bioinformatics IEC-1 Registration, VEI, Oxford Centre for Innovation, Mill
St, Oxford, OX2 0JX, UK.
b) fax to Bioinformatics IEC-1 Registration at +44 1865 793165
c) phone Bioinformatics IEC-1 Registration at +44 1865 793644 

b) Bank Transfer

Your payment can be made in sterling by direct bank transfer
into the following account:

Account Number: 20-6518 40787523
Account Name: Virtual Environments International Ltd
Bank: Barclays Bank, Oxford City Centre Branch,
P.O. Box 333, Oxford, OX1 3HS, UK

--Please ensure your full name is listed with the transfer details.
--You are responsible for any bank charges associated with the
transfer from your bank.
--Please notify us directly of your transfer payment at bioinforg@vei.co.uk.

c) Cheque/Bank Draft

Cheques or bank orders (in pounds or dollars) should be made out to
Virtual Environments International Ltd and mailed to:

Bioinformatics IEC-1 Registration, VEI, Oxford Centre for Innovation, Mill St,
Oxford, OX2 0JX, UK.

Acknowledgement of Registration and Payment:

When you first register at the conference site you should
receive an acknowledgement email with a password and userid.

After receipt of your registration fee you will
receive a further acknowledgement and your userid and password
will be validated to allow access to the conference site
(when it opens).


3) DEADLINE for receipt of ABSTRACT.  

The deadline for receipt of presentation abstracts is Oct 1. Email 
your abstract directly to bioinfabstracts@vei.co.uk. Fuller details of the 
scope of each section is given in the authors' guide accessible via 
http://www.vei.co.uk/bioinfiec1/

Your abstract should be no longer than 300 words. And remember to 
state which forms of presentation you will use (virtual poster presentation, 
virtual lecture, physical poster presentation) you wish and which subject
section the 
presentation is being placed in. For example you 
could present a WWW poster on Visualization in the Virtual Conference and
accompany it 
with a physical poster at the physical conference.  Computers will be
available at the 
physical conference for the presentation and discussion of the virtual
posters and the 
demonstration of software and methods.  

4) DEADLINE for receipt of PRESENTATION

The deadline for receipt of presentations is November 1.  You 
must deposit your text and graphics files at the conference ftp site following
the instructions available at http://www.vei.co.uk/bioinfiec1/. 


Any general e-mails (such as registration queries, maillist queries, 
HTML queries, password queries, timetable queries, general technical 
advice on browsers and graphics, etc) should be sent to:
bioinforg@vei.co.uk

From owner-biophysics@net.bio.net Mon Aug 18 23:00:00 1997
Newsgroups: bionet.biophysics
Path: biosci!news.Stanford.EDU!su-news-hub1.bbnplanet.com!cpk-news-hub1.bbnplanet.com!news.bbnplanet.com!ix.netcom.com!succeed
From: succeed@netcom.com (George Galustian)
Subject: Design testbed for symbiotic systems?
Message-ID: <succeedEF5MG2.H9o@netcom.com>
Organization: Netcom On-Line Services
X-Newsreader: TIN [version 1.2 PL2]
Date: Tue, 19 Aug 1997 09:31:14 GMT
Lines: 3
Sender: succeed@netcom10.netcom.com


-- 
                                             succeed@netcom.com

From owner-biophysics@net.bio.net Mon Aug 18 23:00:00 1997
Path: biosci!daresbury!uninett.no!nntp.uio.no!news-spur1.maxwell.syr.edu!news.maxwell.syr.edu!News1.Vancouver.iSTAR.net!news.istar.net!newsfeed.direct.ca!news-sea-19.sprintlink.net!news-in-west.sprintlink.net!news.sprintlink.net!Sprint!204.238.120.130!jump.net!grunt.dejanews.com!not-for-mail
Date: Tue, 19 Aug 1997 06:33:17 -0600
From: haribol@rocketmail.com
Subject: Who discovered complete change of human body?
Newsgroups: bionet.biophysics
Message-ID: <871823468.18500@dejanews.com>
Organization: Deja News Posting Service
X-Article-Creation-Date: Sun Aug 17 13:11:09 1997 GMT
X-Originating-IP-Addr: 192.108.160.9 (ns.felk.cvut.cz)
X-Http-User-Agent: Mozilla/3.01 (Win95; I)
X-Authenticated-Sender: haribol@rocketmail.com
Lines: 11

Hello!

Could anybody tell me about discovery about complete change of matter in
human body in 5 years period ?
Or just show me sources on internet

Thanks
Alex

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

From owner-biophysics@net.bio.net Mon Aug 18 23:00:00 1997
Path: biosci!BTP8X5.PHY.UNI-BAYREUTH.DE!Klaus.Fritsch
From: Klaus.Fritsch@BTP8X5.PHY.UNI-BAYREUTH.DE (Klaus Fritsch)
Newsgroups: bionet.biophysics
Subject: (no subject)
Date: 19 Aug 1997 03:28:22 -0700
Organization: uni-bayreuth.de
Lines: 2
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <33F9F3C6.4CEB@ep4.phy.uni-bayreuth.de>
References: <succeedEF5MG2.H9o@netcom.com>
NNTP-Posting-Host: net.bio.net

unsubscribe biophys
end

From owner-biophysics@net.bio.net Mon Aug 18 23:00:00 1997
Path: biosci!daresbury!uninett.no!news-feed.inet.tele.dk!cpk-news-hub1.bbnplanet.com!news.bbnplanet.com!newsfeed.direct.ca!news.he.net!news.pagesat.net!news.itis.com!not-for-mail
From: Petr Kuzmic <pkuzmic@biokin.com>
Newsgroups: bionet.biophysics
Subject: Software available: Enzyme kinetics and equilibria
Date: Tue, 19 Aug 1997 10:12:01 -0500
Organization: BioKin Consulting
Lines: 32
Message-ID: <33F9B7C1.92DAD12C@biokin.com>
NNTP-Posting-Host: s47.itis.com
Mime-Version: 1.0
Content-Type: text/plain; charset=us-ascii
Content-Transfer-Encoding: 7bit
X-Mailer: Mozilla 4.01 [en] (Win95; I)
X-Priority: 3 (Normal)

PUBLIC DOMAIN PROGRAM DYNAFIT UPDATED

Program DYNAFIT for the analysis and simulation of enzyme
kinetic and receptor binding data was updated to version
2.17.1 (08/18/97).  It has the capability to analyze multi-
response equilibrium binding data, where several dose res-
ponse curves are analyzed together, while each curve repre-
sents the equilibrium. concentration of a different species.

TEST PROBLEM: NUCLEASE/DNA BINDING MECHANISM

The new features of DYNAFIT are illustrated on complex 
equilibria involved in nuclease catalysis.  Two sets of 
gell-shift data (courtesy Dr. Paul Mitsis, seQ Ltd., Prince-
ton NJ), representing the concentration of (1) the protein
trimer-DNA complex and (2) the hexamer-DNA complex, were 
analyzed together.  The standard error of equibrium constants
was lower than if both datasets are analyzed separately.

LINKS

http://www.biokin.com/dynafit/download.shtml ... program
http://www.biokin.com/dynafit/downexam.shtml ... examples
http://www.biokin.com/dynafit/tutorial/nuclease.shtml

REFERENCES

P. Kuzmic (1996) Anal. Biochem. 237, 260-273.

_____________________________________________________________
Petr Kuzmic Ph.D. * BioKin Ltd. * Madison, WI 53708-8336, USA
pkuzmic@biokin.com * http://www.biokin.com * 608.256.1269 fax

From owner-biophysics@net.bio.net Fri Aug 22 23:00:00 1997
Path: biosci!bcm.tmc.edu!news.msfc.nasa.gov!www.nntp.primenet.com!globalcenter1!news.primenet.com!news.primenet.com!not-for-mail
From: "Mark Flowers <mark@nospam.molec.com" <"-remove nospam">
Newsgroups: bionet.biophysics
Subject: Career opportunities:  Industrial SPM post-doc
Date: 22 Aug 1997 21:36:00 -0700
Organization: Molecular Imaging <http://www.molec.com>
Lines: 96
Message-ID: <5tlpbg$5hq@nntp02.primenet.com>
X-Posted-By: @206.165.23.207 (mflowers)
X-Mailer: Mozilla 4.01 (Macintosh; I; PPC)
MIME-Version: 1.0
X-Priority: 3 (Normal)
Content-Type: text/plain; charset=us-ascii; x-mac-type="54455854"; x-mac-creator="4D4F5353"
Content-Transfer-Encoding: 7bit

Molecular Imaging is currently expanding its industrial post-doc
program.  We have the following positions open:

Polymer SPM Applications Scientist
Biological SPM Applications Scientist
Posted 22 Aug 1997

Molecular Imaging's Industrial Post Doctoral Program, in affiliation
with Arizona State University and Prof. Stuart Lindsay's laboratory :

Two year program leading to exceptional qualifications for either
academic or industrial research careers.

The position will be a combination of:

              research support for current and potential customers
              in house research
              technical sales support
              applications laboratory research and analysis

Collaboration with outside researchers may result in joint authorship,
however this will be entirely at the discretion of the customers. One
can expect that you will be in contact with 2 to 3 dozen research
centers each year. You will be involved in pilot projects using MI
technologies in many leading laboratories, providing many opportunities
for critical publications in a new field.
 
Entrepreneurial / business skills will be empirically taught and each
Post Doc will be part of a team and share leadership as a product
manager for a specific business segment, for example Biological SPM,
Corrosion SPM, Battery SPM, Basic electrochemical SPM, Nanotechnology
SPM, Polymer SPM, etc. Also, territory manager positions are available,
e.g. Japan, Atlantic states, etc.

Sabbatical leave of four weeks will be granted each year for relevant
research collaboration with the researcher of the post doc's choice. An
MI instrument will be loaned to the post doc for the duration of this
sabbatical, and a frugal travel and stipend will be included.

MI perceives this as both a major career opportunity for the post doc
and a service to our customers; therefore, the post doc will be
encouraged to consider significant career opportunities offered by the
MI customer or potential customer base at any time during the 2 years.

Service rewards will be granted. These are:
After one year of post doc service, you will be granted a full SPM
microscope configuration compatible with the controller for your choice.
(DI, TopoMetrix, Park, RHK, or others to come)

In addition, after two years of service (fulfilled post doc), you will
be granted an SPM controller

Upon completion of the 2 years, the post doc may have an opportunity to
head up a specialty niche of MI's application laboratory as Lead
Industrial Scientist or a regional manager position. We must note that
only one such position will be available for each niche although there
are several niches. There may be several post docs for each niche.

If the Lead Industrial Scientist position is filled or not offered, the
post doc will be encouraged to seek positions either in academia or
industry outside of MI.

Through our industrial and academic contacts, MI will provide job search
assistance.

Post doc positions can expect up to 70% travel, some of which may be
international, and long work days and weeks.

Much of this travel will be in support of MI's Manufactures
Representatives and Distributors in working with both current and
potential MI customers in the effective use of MI equipment and in
supporting the customers' research.

You will work as a team member and will share in sales commission bonus
with all MI staff.

Success in this position will require both exceptional problem solving
skills (theoretical and practical) and a strong acumen for the use of
analytical instrumentation and designing enhancements for scientific
instrumentation.

See the Molecular Imaging web site (http://www.molec.com) for further
details about the company and research.

E-mail (no attachments) full CV including list of papers or posters and
references to geos@molec.com

Note: if you have html's of your publications, application notes, or
images, also include addresses.
Come talk to us at locations listed on the MI calendar. 
(http://www.molec.com/calendar/index.html)
 
 
 
 


From owner-biophysics@net.bio.net Fri Aug 22 23:00:00 1997
Path: biosci!bcm.tmc.edu!news.msfc.nasa.gov!infeed1.internetmci.com!newsfeed.internetmci.com!192.48.96.126!in2.uu.net!202.82.1.1!bull.hkstar.net!hkstar2!news
From: "Wong Kam Hung" <chdragon@hkstar.com>
Newsgroups: bionet.biophysics
Subject: Centripetal Force
Date: 23 Aug 1997 10:20:42 GMT
Organization: HK & Kln CCPA MCS Sec. Sch.
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           There are two equations about centripetal force. They are
a=(v^2)/r and a=(£s^2)r . Could anyone tell me which of the following
concepts is correct?
        1) By a=(v^2)/r ,  when  r  decreases, a  increases.
        2) By  a=(£s^2)r , when r  decreases, a decreases too.
where  v is the linear velocity and £s is the angular velocity. 
        If you can solve this problem, please send your answer to me.
Thanks!

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<html><head></head><BODY bgcolor=3D"#FFFFFF"><p><font size=3D2 =
color=3D"#000000" face=3D"=B2=D3=A9=FA=C5=E9"> =
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;There are =
two equations about centripetal force. They are a=3D(v^2)/r and =
a=3D(=A3s^2)r . Could anyone tell me which of the following concepts is =
correct?<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;1) By a=3D(v^2)/r =
, &nbsp;when &nbsp;r &nbsp;decreases, a &nbsp;increases.<br> =
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;2) By &nbsp;a=3D(=A3s^2)r , =
when r &nbsp;decreases, a decreases too.<br>where &nbsp;v is the linear =
velocity and =A3s is the angular velocity. <br> =
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;If you can solve this problem, =
please send your answer to me. Thanks!</p>
</font></body></html>
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From owner-biophysics@net.bio.net Sat Aug 23 23:00:00 1997
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From: Pascal_Bochet@brown.edu (Pascal_Bochet)
Newsgroups: bionet.biophysics
Subject: Re: Centripetal Force
Date: 24 Aug 1997 15:00:05 GMT
Organization: Brown University, Providence, RI -- USA
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In article <01bcafae$133a7620$ec1752ca@default>, chdragon@hkstar.com says...
>
>This is a multi-part message in MIME format.
>
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>
>           There are two equations about centripetal force. They are
>a=(v^2)/r and a=(£s^2)r . Could anyone tell me which of the following
>concepts is correct?
>        1) By a=(v^2)/r ,  when  r  decreases, a  increases.
>        2) By  a=(£s^2)r , when r  decreases, a decreases too.
>where  v is the linear velocity and £s is the angular velocity. 
>        If you can solve this problem, please send your answer to me.
>Thanks!
>
With this notations:
 v=£s*r and both expressions are the same.
v is the speed and £s the angulkar velocity.
That 's it.

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><html><head></head><BODY bgcolor=3D"#FFFFFF"><p><font size=3D2 =
>color=3D"#000000" face=3D"=B2=D3=A9=FA=C5=E9"> =
>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;There are =
>two equations about centripetal force. They are a=3D(v^2)/r and =
>a=3D(=A3s^2)r . Could anyone tell me which of the following concepts is =
>correct?<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;1) By a=3D(v^2)/r =
>, &nbsp;when &nbsp;r &nbsp;decreases, a &nbsp;increases.<br> =
>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;2) By &nbsp;a=3D(=A3s^2)r , =
>when r &nbsp;decreases, a decreases too.<br>where &nbsp;v is the linear =
>velocity and =A3s is the angular velocity. <br> =
>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;If you can solve this problem, =
>please send your answer to me. Thanks!</p>
></font></body></html>
>------=_NextPart_000_01BCAFF1.215DB620--
>


From owner-biophysics@net.bio.net Sun Aug 24 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!howland.erols.net!torn!garnet.nbnet.nb.ca!news.unb.ca!coranto.ucs.mun.ca!plato.ucs.mun.ca!wmfry
From: Mark Fry <wmfry@morgan.ucs.mun.ca>
Newsgroups: bionet.biophysics
Subject: neuron simulators
Date: Mon, 25 Aug 1997 17:53:39 -0230
Organization: Memorial University of Newfoundland
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can anybody tell me what neuron simulation software packages are avaiable.
I want to run some simulations, and found that 'Neuron" from yale looks to
be the most complete, but it is not very user friendly.

I am looking for the simplest package that will allow me to insert my own
channels, and determine their spatial distribution.

thanks in advance

Mark Fry                                    ribit    @..@         
4th floor BMS Fac of Med.                        \  (----)                  
Memorial University of NFLD                        ( >**< )             
A1B 3V6                                           ^^^""""^^^
wmfry@plato.ucs.mun.ca                          (ASCII Xenopus)


From owner-biophysics@net.bio.net Mon Aug 25 23:00:00 1997
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From: simon <mariapi@mbox.vol.it>
Newsgroups: bionet.biophysics
Subject: HELP!!!!
Date: Fri, 22 Aug 1997 20:01:22 +0200
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I must find some document about energy and mass balance.
Is there someone that can tell me where i can find it on internet?

Thank you.




From owner-biophysics@net.bio.net Mon Aug 25 23:00:00 1997
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From: bali@necker.fr (Moez BALI)
Newsgroups: bionet.biophysics
Subject: Re: HELP!!!!
Date: Tue, 26 Aug 1997 18:41:36 +0100
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In article <33FDD3F1.1428D7B9@mbox.vol.it>, simon <mariapi@mbox.vol.it> wrote:

> I must find some document about energy and mass balance.
> Is there someone that can tell me where i can find it on internet?
> 
> Thank you.

try this link : http://lenti.med.umn.edu/~mwd/courses.html

From owner-biophysics@net.bio.net Tue Aug 26 23:00:00 1997
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From: tivol@news.wadsworth.org (William Tivol)
Newsgroups: bionet.biophysics
Subject: Re: Centripetal Force
Date: 27 Aug 1997 21:26:41 GMT
Organization: Wadsworth Center, NY Health Dept.
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Wong Kam Hung (chdragon@hkstar.com) wrote:

:            There are two equations about centripetal force. They are
: a=(v^2)/r and a=(omega^2)r . Could anyone tell me which of the following
: concepts is correct?
:         1) By a=(v^2)/r ,  when  r  decreases, a  increases.
:         2) By  a=(omega^2)r , when r  decreases, a decreases too.
: where  v is the linear velocity and omega is the angular velocity. 
:         If you can solve this problem, please send your answer to me.
: Thanks!

	No problem.  Since the angular velocity for circular motion is
just v/r, the two formulas are equivalent.  For other motion, you need
the tangential component of the velocity (not the radial component),
and the two are still equivalent.
				Yours,
				Bill Tivol







































From owner-biophysics@net.bio.net Thu Aug 28 23:00:00 1997
Path: biosci!QM.YALE.EDU!Hui-Zhang
From: Hui-Zhang@QM.YALE.EDU (hui zhang)
Newsgroups: bionet.biophysics
Subject: http://www.bio.net/hypermail/BIOPHYSICS/
Date: 29 Aug 1997 15:10:48 -0700
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Postdoctoral Position in Mammalian Cell Cycle Regulation.

Available immediately to investigate the molecular basis of mammalian 
cell cycle regulation and the consequences of its alteration during 
tumorigenesis (references: Genes & Devel. 8, 1750-1758; Cell 82, 
915-925).  We are particularly interested in the mechanisms of G1/S and 
G2/M checkpoint control, DNA damage response, apoptosis, and cellular 
senescence/immortalization.  Candidates must have a Ph. D. and/or M. D. 
degree and experience in genetics, biochemistry, molecular or cell 
biology is required for the position.  

Please send the curriculum vitae and the names of three references to:

Dr. Hui Zhang
Department of Genetics
Yale University School of Medicine
333 Cedar Street
New Haven, CT 06520



From owner-biophysics@net.bio.net Sat Aug 30 23:00:00 1997
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From: Petr Kuzmic <pkuzmic@biokin.com>
Newsgroups: bionet.biophysics
Subject: Software update: Enzyme kinetics and equilibria
Date: Sat, 30 Aug 1997 20:53:33 -0500
Organization: BioKin Consulting
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==========================================================
                     PUBLIC DOMAIN PROGRAM DYNAFIT UPDATED

Program DYNAFIT for the analysis and simulation of enzyme
kinetic and receptor binding data was updated to version
2.17.2 (08/29/97).  
__________________________________________________________
               NOTATION FOR ANALYSIS OF COMPLEX EQUILIBRIA 

The notation for the regression analysis of equilibrium 
data was simplified.  We no longer have to specify both 
rate constants for a reversible step, A+B <===> AB : k1 k2,
but instead we can use the shorthand notation A + B  <===> 
AB : K  equil, where K is an equilibrium constant and 
'equil' (or 'equilibrium') is a new keyword.
__________________________________________________________
     ON-LINE TUTORIAL: NONSPECIFIC LIGAND/RECEPTOR BINDING

The new features of DYNAFIT are illustrated on complex 
equilibria that include two-site co-operative ligand binding,
accompanied by nonspecific interactions.  The same data 
(due to Gary Knott of Civilized Software Inc.) are featured
in the "Software Solution" column of the most recent 
"HMS Beagle" newsletter (August 14).

__________________________________________________________
                                                     LINKS

http://www.biokin.com/dynafit/index.shtml ... DYNAFIT home
http://www.biokin.com/dynafit/tutorial/index.shtml 
http://www.biokin.com/dynafit/tutorial/nonspec.shtml
http://www.biokin.com/dynafit/manual/userman.shtml 
http://www.biokin.com/home/whatsnew.shtml
http://biomednet.com/hmsbeagle/1997/14/booksoft/softsol.htm

_____________________________________________________________
Petr Kuzmic Ph.D. * BioKin Ltd. * Madison, WI 53708-8336, USA
pkuzmic@biokin.com * http://www.biokin.com * 608.256.1269 fax

From owner-biophysics@net.bio.net Sat Aug 30 23:00:00 1997
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From: pPouard.laennec@invivo.edu
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Newsgroups: bionet.biophysics
Distribution: world
Subject: Platelets biomechanic
Date: Sun, 31 Aug 1997 11:51:32 GMT
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who knows where I could find references about thr biomechanic of platelets? 



From owner-biophysics@net.bio.net Sun Aug 31 23:00:00 1997
Path: biosci!KITTEN.CHEM.UH.EDU!gao
From: gao@KITTEN.CHEM.UH.EDU (Xiaolian Gao)
Newsgroups: bionet.biophysics
Subject: NMR/Computation postdoctoral position
Date: 1 Sep 1997 10:14:08 -0700
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Applications are invited for an NMR/Computation postdoctoral position in
the Chemistry Department at the University of Houston.  Experiences in high
resolution structural NMR and/or molecular modeling areas are highly
desirable.  Houston has seen a rapid growth in development of
biotechnology.  Our NMR Laboratory is a member of the Institute for
Molecular Design and the joint biophysical training programs involving
several Universities in the area.  Strong candidates may also be considered
for the NIH postdoctoral fellowship (citizenship or permanent residence is
required).  The position offers an excellent opportunity for scientific
excitement and career advancement.  Salary is highly competitive and
commensurate with experience.  Please send resume and three letters of
reference to Dr. Xiaolian Gao, Department of Chemistry, University of
Houston, Houston, TX  77204-5641.  
Email: gao@kitten.chem.uh.edu
Web sites:
http://www.chem.uh.edu/www/gao/intro.html
http://www.bioc.rice.edu
http://condor.bcm.tmc.edu/SCBMB/scbmb.html

Xiaolian (pronounce as Shao-lin) Gao
Dept. Chemistry
University of Houston
Houston, TX 77204-5641
Tel: 713 743-2805, 2806   Fax: 713 743-2709
gao@kitten.chem.uh.edu  or xgao@uh.edu

