From owner-biotechniques@net.bio.net Mon Mar 03 22:00:00 1997
Path: biosci!biosci!not-for-mail
From: John Brennand <john.brennand@gbapr.zeneca.com>
Newsgroups: bionet.journals.letters.biotechniques
Subject: Re: 96-well amino coated microtitre plates
Date: 4 Mar 1997 13:42:48 -0800
Organization: Zeneca Pharmaceuticals
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derek

costar (01494 471207) have a range of plates with different surface
chemistrys.

john

From owner-biotechniques@net.bio.net Mon Mar 03 22:00:00 1997
Path: biosci!biosci!not-for-mail
From: Mail@scri.sari.ac.uk
Newsgroups: bionet.journals.letters.biotechniques
Subject: 96-well amino coated microtitre plates
Date: 4 Mar 1997 05:54:58 -0800
Organization: Scottish Crop Research Institute
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Hello

I am looking for a supplier of 96-well amino coated microtitre plates.  Can 
any one help?

Cheers

Dr Derek Stewart

d.stewart@scri.sari.ac.uk

From owner-biotechniques@net.bio.net Mon Mar 03 22:00:00 1997
Path: biosci!biosci!not-for-mail
From: Keld Sorensen <KeldS@uic.edu>
Newsgroups: bionet.journals.letters.biotechniques
Subject: Re: 96-well amino coated microtitre plates
Date: 4 Mar 1997 13:44:32 -0800
Organization: University of Illinois, College of Medicine
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Nunc used to carry plates coated with secondary amines. Lately I have
received a flyer saying that they now carry ones coated with primary
amines which theoretically should be advantageous.

Corning-Costar carries various plates (NHS coated, i.e. NH2 reactive),
COOH, and some additional ones.

Pierce carries a long list of "activated" and "coated" plates
maleic anhydride (NH2 reactive), NeutrAvidin, Streptavidin, Protein A,
Protein G, Goat anti Mouse, Glutathione, Metal Chelate, Dextrin and
more.

From owner-biotechniques@net.bio.net Thu Mar 13 22:00:00 1997
Path: biosci!biosci!not-for-mail
From: Neuronal Virus <inseong@plaza.snu.ac.kr>
Newsgroups: bionet.journals.letters.biotechniques
Subject: How can I solubilize my protein for FPLC injection?
Date: 14 Mar 1997 05:37:19 -0800
Organization: Dondamoa Co., Ltd.
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Keywords: Protein solubilizing

This is a multi-part message in MIME format.

------=_NextPart_000_01BC3070.D08E7A40
Content-Type: text/plain; charset=EUC-KR
Content-Transfer-Encoding: 7bit

I am trying to solubilize my protein which was desalted and lyophilized for
further purification by FPLC.
But it defied to be solved in small amount of solvent (e.g., water). 
Injection solution should be, as you well know, as small amount as
possible.
  Maybe the protein has hydrophobic patches outside and aggregates each
other or its concentration is too high to be dissolved in.  But whenever I
diluted it enough, its peak was hard to recognize.  Have you experienced
this type of dilemma? 
Any suggestions and opinions will be a great help!

------=_NextPart_000_01BC3070.D08E7A40
Content-Type: text/html; charset=ISO-2022-KR
Content-Transfer-Encoding: quoted-printable

=1B$)C<html><head></head><BODY bgcolor=3D"#FFFFFF"><p><font size=3D2 =
color=3D"#000000" face=3D"Arial">I am trying to solubilize my protein =
which was desalted and lyophilized for further purification by =
FPLC.<br>But it defied to be solved in small amount of solvent (e.g., =
water). &nbsp;Injection solution should be, as you well know, as small =
amount as possible.<br> &nbsp;Maybe the protein has hydrophobic patches =
outside and aggregates each other or its concentration is too high to be =
dissolved in. &nbsp;But whenever I diluted it enough, its peak was hard =
to recognize. &nbsp;Have you experienced this type of dilemma? <br>Any =
suggestions and opinions will be a great help!<br><br></p>
</font></body></html>
------=_NextPart_000_01BC3070.D08E7A40--


From owner-biotechniques@net.bio.net Fri Mar 14 22:00:00 1997
Path: biosci!biosci!not-for-mail
From: MMCCARTHY@biotechnet.com
Newsgroups: bionet.journals.letters.biotechniques
Subject: BioTechniques 22(4), April 1997
Date: 15 Mar 1997 09:30:13 -0800
Organization: BIOSCI International Newsgroups for Molecular Biology
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BioTechniques 22(4), April 1997
Table of Contents

BENCHMARKS

Chemiluminescent detection of protein
molecular weight markers in Western blot
techniques
     Liu R.H., J. Jacob and B. Tennant

Southern blotting of long-term preserved DNA
     Laniel M.-A., M. El-Amine, G. Boire and
     H.-A. Menard

Low-power vacuum apparatus for blotting
     Passey R.J.

Increased 32P-SSCP sensitivity by combining
restriction enzyme-digestion and extended
X-ray film exposures
     Lovlie R. and H.G. Eiken

Separation of DNA strands facilitates
detection of point mutations by PCR-SSCP
     Selvakumar N., B.-C. Ding and S.M.
     Wilson
     
Improved resolution of asymmetric-PCR SSCP
products
     Pokorny R.M., A.B. Dietz, S. Galandiuk
     and H.L. Neibergs

DNA template as a source of artifact in the
detection of p53 gene mutations using
archived tissue
     Shiao Y.-H., G.S. Buzard, C.M. Weghorst
     and J.M. Rice

Easy method for the cloning of mammalian cell
colonies
     Thompson J.A. and G. Ioli

Two-layer gradient isolation of rat
peritoneal mast cells
     Price J.A.

Micropreparation of cultured cells for in
situ reverse transcription PCR
     Zhang H. and S. Wadler

Site-directed mutagenesis using a PCR-based
staggered re-annealing method without
restriction enzymes
     Ailenberg M. and M. Silverman


Semiquantitative RT-PCR: Enhancement of assay
accuracy and reproducibility
     Saric T. and S.A. Shain

Direct PCR from paraffin-embedded tissue
     Burns W.C., Y.S. Liu, C. Dow, R.J.S.
     Thomas and W.A. Phillips

Bandstab: a PCR-based alternative to
cloning PCR products
     Wilton S., L. Lim, D. Dye and N. Laing

Sequential extraction of DNA and DNA-binding
proteins from low cell numbers
     El-Osta S., P. Kantharidis and J.R.
     Zalcberg

Non-radioisotopic identification of
endonucleases involved in apoptosis
     Boone D.L. and B.K. Tsang

Easy gene walking
     Harrison R.W., J.C. Miller, M.J. D'Souza
     and G. Kampo

Automated fluorescent DNA sequencing by a
simplified solid-phase chemical sequencing
method
     Ohara R., A. Tanaka and O. Ohara

Microassay for the assessment of low
levels of hydroxyproline
     Creemers L.B., D.C. Jansen, A. van
     Veen-Reurings, T. van den Bos and V.
     Everts


THE INTERNET ON-RAMP
     Cyberspace for Biologists


SHORT TECHNICAL REPORTS

Northern blotting of RNA denatured in glyoxal
without buffer recirculation
     Burnett W.V.

Identification of recombinant baculoviruses
using green fluorescent protein as a
selectable marker
     Wilson L.E., N. Wilkinson, S.A. Marlow,
     R.D. Possee and L.A. King

Determination of human NAT2 acetylator
genotype by oligonucleotide ligation assay
     Bigler J., C. Chen and J.D. Potter

Detection of DNA polymorphisms by fluorescent
RAPD analysis
     Corley-Smith G.E., C.J. Lim, G.B. Kalmar
     and B.P. Brandhorst

Quantitative analysis of 16S rDNA using
competitive PCR and the QPCR System 5000
     Blok H.J., A.M. Gohlke and A.D.L.
     Akkermans

Analysis of 3H-proline-labeled protein
by rapid filtration in multiwell plates for
the study of collagen metabolism
     Koyano Y., H. Hammerle and J.
     Mollenhauer


RESEARCH REPORTS

Recombinant HMG1 protein produced in Pichia
pastoris: a non-viral gene delivery agent
     Mistry A.R., L. Falciola, L. Monaco, R.
     Tagliabue, G. Acerbis, A. Knight, R.P.
     Harbottle, M. Soria, M.E. Bianchi, C.
     Coutelle and S.L. Hart

Expression of foreign proteins on the surface
of Autographa californica nuclear
polyhedrosis virus
     Grabherr R., W. Ernst, O. Doblhoff-Dier,
     M. Sara and H. Katinger

High sensitivity of laser-induced
fluorescence detection in capillary gel
electrophoresis for accurate apolipoprotein
E-genotyping
     Schlenk A., K. Bohnet, D. Aguillon, C.
     Lafaurie, G. Siest and S. Visvikis

Heat-mediated activation of
affinity-immobilized Taq DNA polymerase
     Nilsson J., M. Bosnes, F. Larsen, P.-A.
     Nygren, M. Uhlen and J. Lundeberg


PRODUCT APPLICATION FOCUS

Rainbow Universal CPG: a versatile solid
support for oligonucleotide synthesis
     Nelson P.S., S. Muthini, M. Vierra, L.
     Acosta and T.H. Smith

ThermoSequenase DNA Polymerase and T.
acidophilum pyrophosphatase:  New
thermostable enzymes for DNA sequencing
     Vander Horn P.B., M.C. Davis, J.J.
     Cunniff, C. Ruan, B.F. McArdle, S.B.
     Samols, J. Szasz, G. Hu, K.M. Hujer,
     S.T. Domke, S.R. Brummet, R.B. Moffett
     and C.W. Fuller


NEW PRODUCTS
INDEX TO ADVERTISERS

From owner-biotechniques@net.bio.net Mon Mar 17 22:00:00 1997
Path: biosci!biosci!not-for-mail
From: Jan Marten de Jong <j.m.dejong@student.utwente.nl>
Newsgroups: bionet.journals.letters.biotechniques
Subject: philosophy paper
Date: 18 Mar 1997 06:23:01 -0800
Organization: Universiteit Twente
Lines: 22
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L.S.,

My name is Jan Marten de Jong. I'm a student of the university of Twente
(netherlands) and I'm studying applied communications.

This trimester I have to make an essay for Philosophy. I'd like to do it
about bio-technology. More specificly, about identification (DNA
fingerprinting for crime, insurance issues, screening of large populations,
etc.)

Now I wondered if maybe anyone had written about this subject. Maybe there
is some information on the net about it. Or someone has an article about
it. It doesn't matter what it is, I can use (almost) everything.

If you have something for me, you can mail me
(j.m.dejong@student.utwente.nl) or you can post it in this newsgroup.

Thanks already!



Jan Marten de Jong

From owner-biotechniques@net.bio.net Wed Mar 19 22:00:00 1997
Path: biosci!biosci!not-for-mail
From: BIOSCI Administrator <biohelp@net.bio.net>
Newsgroups: bionet.journals.letters.biotechniques
Subject: BIOSCI/bionet miniFAQ & Fundraiser
Date: 20 Mar 1997 06:00:46 -0800
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 239
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(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.

				Sincerely,

				Dave Kristofferson
				BIOSCI/bionet Manager

				biosci-help@net.bio.net

From owner-biotechniques@net.bio.net Thu Mar 27 22:00:00 1997
Path: biosci!biosci!not-for-mail
From: John Brandt <jbrandt@ngi.com>
Newsgroups: bionet.journals.letters.biotechniques
Subject: Non-radioactive labelling
Date: 28 Mar 1997 13:55:39 -0800
Organization: National Genetics Institute
Lines: 6
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I currently use digoxigenin-labelled probes and a colorimetric detection
assay using anti-DIG antibodies (NBT/BCIP). I want to incorporate
fluorescent detection. I would like feedback on anti-DIG-fluorescein,
-rhodamine, -AMCA, or other detection methods.

Thank you, in advance, for any suggestions.

From owner-biotechniques@net.bio.net Mon Mar 31 23:00:00 1997
Path: biosci!biosci!not-for-mail
From: Rolf Kocherhans <rolfk@vetvir.unizh.ch>
Newsgroups: bionet.journals.letters.biotechniques
Subject: Free molbio prg. available here !
Date: 1 Apr 1997 05:37:21 -0800
Organization: University of Zurich
Lines: 42
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Hi there

I am presently looking for molecular biologists willing to test some
programs I made aimed to speeding up the daily lab work !

- This is how it works:

The programs are accessible over the WWW, all you have to do is download
a free plugin to enhance the browser you are using (Netscape 2.x or
Internet Explorer 2.x or higher) on your Mac or Windows computer !

- What you have to do first:

Download the appropriate plugin and install it on your computer, here is
the URL:

http://www.unizh.ch/vetvir/plugin.html

- Then connect to:

http://www.unizh.ch/vetvir/programs.html


These are the programs which make your live as a molecular biologist
easier !

a. Digest Preview enter the size(s) of your DNA fragment(s) and see
their migration pattern in a virtual gel in comparison to a 1 kb ladder.

b. Dilution Calculator does all the calculations when you have to make
up solutions.

c. Adaptor Design helps to create adaptors in order to link incompatible
DNA ends together,in frame !

there many others: Oligo Tm,Compatible ends etc.


Please have a look and comment !

Regards
Rolf Kocherhans   mailto:rolfk@vetvir.unizh.ch

