From owner-diagnostics@net.bio.net Tue Jun 02 23:00:00 1998
Path: biosci!biosci!not-for-mail
From: BIOSCI Administrator <biohelp@net.bio.net>
Newsgroups: bionet.diagnostics
Subject: BIOSCI/bionet miniFAQ & Fundraiser
Date: 3 Jun 1998 02:27:15 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
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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.


From owner-diagnostics@net.bio.net Wed Jun 03 23:00:00 1998
Path: biosci!biosci!not-for-mail
From: Mark Cauchi <Mark.Cauchi@med.monash.edu.au>
Newsgroups: bionet.diagnostics
Subject: Recombinant DNA Techniques Course
Date: 4 Jun 1998 01:29:11 -0700
Organization: Monash University
Lines: 8
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The Micromon Unit at the Department of Microbiology, Monash University
in Melbourne, Australia will be running its Recombinant DNA Techniques
Course between the 15-20 November, 1998.  This is an
introductory-intermediate level course which offers a skills-based
training package.  If you would like further information, details can be
found on our web page at

http://www.med.monash.edu.au/micro/department/dnacorse.htm

From owner-diagnostics@net.bio.net Thu Jun 18 23:00:00 1998
Path: biosci!biosci!not-for-mail
From: Shammas <shammas@online.no>
Newsgroups: bionet.diagnostics
Subject: mRNA and Taq polymerase
Date: 19 Jun 1998 02:33:41 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 1
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Why does Taq polymerase work only on cDNA and not mRNA?

From owner-diagnostics@net.bio.net Thu Jun 18 23:00:00 1998
Path: biosci!biosci!not-for-mail
From: RSA <rathbun@sedona.net>
Newsgroups: bionet.diagnostics
Subject: POSITION: Statistician/Systems Scientist
Date: 19 Jun 1998 03:19:18 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 37
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Statistician/Systems Scientist

Position Description:  We are seeking a statistician for the
characterization and evaluation of sophisticated instrument systems in
the medical diagnostics industry. 

Responsibilities:
=B7 Work with engineers and scientists to develop and execute
sophisticated designed experiments.
=B7 Creation and maintenance of a SAS Macro library
=B7 Design experiments that quantify sources of variability and lead to
improvements in system performance.

Qualifications
=B7 Read/convert data from various sources (text files, Oracle
databases, ODBC).
=B7 Ideally, familiar with the characterization and evaluation of
sophisticated instrument systems in the diagnostics industry.
=B7 Familiar with statistical analysis and interpretation of complex
data sets.
=B7 Solid working knowledge and experience in the application of
statistical techniques (t-tests, ANOVA, Design of Experiments,
Boot-strapping, etc.)

If you have an interest in this or other opportunities, please send us
your resume/CV as an Attached File to an email or send by mail/FAX to
RS&A to the attention of Ann Rathbun, Managing Director. All
correspondence is held in strict confidence.


Rathbun, Sapir & Associates
P.O. Box 2337  
Sedona, AZ 86339-2337 * USA
(520) 203-0074 Office  (520) 203-0075 FAX 
E-mail: rathbun@sedona.net



From owner-diagnostics@net.bio.net Thu Jun 18 23:00:00 1998
Path: biosci!biosci!not-for-mail
From: Shammas <shammas@online.no>
Newsgroups: bionet.diagnostics
Subject: amplitagold Taq polymerase
Date: 19 Jun 1998 02:33:22 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 3
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I noticed that using amplitagold Taq polymerase in PCR gives a double 
band of the amplicon but not with ordinary Taq polymerase. Has anybody 
experienced anything similar and what may be the explanation ?

From owner-diagnostics@net.bio.net Sun Jun 21 23:00:00 1998
Path: biosci!biosci!not-for-mail
From: Gunnaporn Veerachato <vgunnapo@chula.ac.th>
Newsgroups: bionet.diagnostics
Subject: Q:The eradication program of CSFV?
Date: 22 Jun 1998 01:01:38 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 9
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Dear all
    I have heard that Denmark is one of the classical swine fever virus
(CSFV) free area. Could anyone please tell me the diagnostic
methods and eradication program of CSFV in Denmark?

Thanks in advance

Gunnaporn  Veerachato


From owner-diagnostics@net.bio.net Sun Jun 21 23:00:00 1998
Path: biosci!biosci!not-for-mail
From: naimi secretary <naimi@ssmain.uniss.it>
Newsgroups: bionet.diagnostics
Subject: NAIMI congress
Date: 22 Jun 1998 08:47:25 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 47
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<html>
<font face="Times New Roman, Times">Dear, <br>
<br>
The University of Sassari, Sardinia, Italy, supports initiatives centred
around the theme of scientific research in the framework of EU policies
promoting transnational scientific co-operation among European and other
countries. In particular, the University of Sassari is organising a round
table entitled: <br>
<br>
<i><div align="center">
Scientific research in Mediterranean Countries in the framework of EU
programmes:<br>
current status and perspectives<br>
<br>
</i></div>
The round table will take place on September 5th at the &quot;Porto Conte
Ricerche&quot; centre, (Alghero, SS, Sardinia), as part of the NAIMI
symposium (Nucleic Acids and their Interactions with Metal Ions), a
satellite symposium of the ICCC Congress (International Conference on
Coordination Chemistry - Florence). <br>
<br>
We would be very glad if a representative of your Agency/Organisation
would be interested in participating in the round table; we believe that
this event will provide a good opportunity to exchange information on EU
policies for the support of international research projects, and possibly
offer some ideas on forms of co-operation between EU and non EU
countries.<br>
<br>
In order to further promote closer links between the world of research
and Public Support Agencies, we are also forwarding an invitation to main
Universities/Research Institutes from various countries to submit
applications by a young scientist (under 35 years of age)to participate
in the works of the NAIMI symposium. <br>
<br>
We are looking forward to your kind reply, and are at your disposal for
any further information you may request.<br>
<br>
Yours sincerely<br>
<br>
 Prof. Maria Luisa Ganadu<br>
<br>
<br>
For further information about NAIMI Congress, please contact
</font><font color="#0000FF"><u>naimi@ssmain.uniss.it</font></u><font color="#000000">
<br>
</font></html>


From owner-diagnostics@net.bio.net Mon Jun 22 23:00:00 1998
Path: biosci!biosci!not-for-mail
From: Cramoy <cramoy@aol.com>
Newsgroups: bionet.diagnostics
Subject: Accuracy of T-cell stimulation test
Date: 23 Jun 1998 01:37:41 -0700
Organization: AOL http://www.aol.com
Lines: 29
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I am looking for information on the accuracy, or lack thereof, of T-cell
stimulation tests (mitogen stimulation tests) specifically for the detection of
Borrelia burgdorferi (causal agent in Lyme disease).  I have done a literature
search of the abstracts, but am looking for specific info on 
	1.  Cross-reactivity with other spirochetes (With which spirochetes is it
likely to cross-react?  How frequent is this cross-reactivity, etc.), 
	2.  Does test cross-react with non-spirochetal bacteria, (if so which ones and
any theories on why)? 
	3.  What are estimated numbers for the occurrence of other spirochetes in the
general population?  
	4.  Are there specific antigen tests to rule out infection by other
spirochetes that may cross-react?  And, if so, are these antigen tests anymore
reliable than the ones currently available for Borrelia burgdorferi?  
	5.  What are the chances that a test result more than 3 standard deviations
above the norm for Borrelia burgdorferi is really due to cross-reactivity and
has no significance in diagnosing Lyme disease?  Does the usual meaning of
standard deviations get thrown out the window due to cross-reactivity in this
case?

I would appreciate personal insights from researchers and laboratory personnel
familiar with this topic, literature references that are worth reading in their
entirety rather than as abstracts, references for textbooks or monographs that
will contain detailed information that will help to sort out these questions.

Thank you,

	Carolyn Cramoy, M. S.



From owner-diagnostics@net.bio.net Wed Jun 24 23:00:00 1998
Path: biosci!biosci!not-for-mail
From: Yokhom Shasketper <wis_useco@gnwmail.com>
Newsgroups: bionet.diagnostics
Subject: Chlamydia/S.abortusovis antibodies
Date: 25 Jun 1998 08:03:01 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 27
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Hi!

 We are going to collect ovine sera from different animals vaccinated with an ovine  Chlamydia  - Salmonella abortusovis vaccine for  a practice work on  immunological responses. Although our old bi
liographic protocols suggest the complement fixation test to discover antibody levels in vaccinated-sheep, we don't know a supplier for ovine sera (positive control) against Chlamydia or S.abortusov
s (to be used in complement fixation test).  Moreover, these protocols need  antigen standardisation.

We believe ELISA test in routine will be the best assay to replace the CF' test for Chlamydia antibody  (there are several ELISA kits in the market). Are there any  correlation between the CF' titre
and the ELISA titre?.

Our decision about  S.abortus is more difficult. Tube or slide agglutination test are very easy to do, but what kind of purified antigen we have to use on routine tests (the antigenic formulae of  S
abortusovis is 4,12:c:1,6). Moreover, Have these tests enough sensibility to quantify an inmunological  response by vaccination?. Is it possible to establish an titre of inmunological status?
 Could anyone suggest us any test for our investigation?. 


We would appreciate any comment. 
Thanks a lot in advance,


Yokhom Shasketper




__________________________________________________________
Get Your FREE Email address at http://www.GNWmail.com/
GNWmail.com - International free e-mail in your language

From owner-diagnostics@net.bio.net Thu Jun 25 23:00:00 1998
Path: biosci!biosci!not-for-mail
From: wis-useco@usa.net
Newsgroups: bionet.diagnostics
Subject: Chlamydia/S.abortusovis antibodies
Date: 26 Jun 1998 01:30:36 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 24
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Approved: odonnell@sasa.gov.uk
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NNTP-Posting-Host: net.bio.net

Hi!

 We are going to collect ovine sera from different animals vaccinated with an ovine  Chlamydia  - Salmonella abortusovis vaccine for  a practice work on  immunological responses. Although our old bi
liographic protocols suggest the complement fixation test to discover antibody levels in vaccinated-sheep, we don't know a supplier for ovine sera (positive control) against Chlamydia or S.abortusov
s (to be used in complement fixation test).  Moreover, these protocols need  antigen standardisation.

We believe ELISA test in routine will be the best assay to replace the CF' test for Chlamydia antibody  (there are several ELISA kits in the market). Are there any  correlation between the CF' titre
and the ELISA titre?.

Our decision about  S.abortus is more difficult. Tube or slide agglutination test are very easy to do, but what kind of purified antigen we have to use on routine tests (the antigenic formulae of  S
abortusovis is 4,12:c:1,6). Moreover, Have these tests enough sensibility to quantify an inmunological  response by vaccination?. Is it possible to establish an titre of inmunological status?
 Could anyone suggest us any test for our investigation?. 


We would appreciate any comment. 
Thanks a lot in advance,


Yokhom Shasketper



____________________________________________________________________
Get free e-mail and a permanent address at http://www.netaddress.com/?N=1

From owner-diagnostics@net.bio.net Thu Jun 25 23:00:00 1998
Path: biosci!biosci!not-for-mail
From: Wjd4u <wjd4u@aol.com>
Newsgroups: bionet.diagnostics
Subject: EKG
Date: 26 Jun 1998 01:31:04 -0700
Organization: AOL http://www.aol.com
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I need information on the absence of R-wave on an EKG.

From owner-diagnostics@net.bio.net Thu Jun 25 23:00:00 1998
Path: biosci!biosci!not-for-mail
From: mylove502@my-dejanews.com
Newsgroups: bionet.diagnostics
Subject: Re: mRNA and Taq polymerase
Date: 26 Jun 1998 02:39:21 -0700
Organization: Deja News - The Leader in Internet Discussion
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You have to use Reverse Transcriptase because it is the only enzyme to
synthesize cDNA from mRNA. If you want to amplify DNA from mRNA, you will use
two step reactions. First, you will get cDNA from reverstranscription using
RTase and then you can amplify numerous DNA molecules using PCR. Taq DNA
polymerase is used in this step.


From: Shammas <shammas@online.no>
Newsgroup: bionet.diagnostics
Date: 1998? 6? 19? ??? PM 6:33
Subject: mRNA and Taq polymerase


>Why does Taq polymerase work only on cDNA and not mRNA?

-----== Posted via Deja News, The Leader in Internet Discussion ==-----
http://www.dejanews.com/   Now offering spam-free web-based newsreading

From owner-diagnostics@net.bio.net Thu Jun 25 23:00:00 1998
Path: biosci!biosci!not-for-mail
From: AMBID <m.miles@lshtm.ac.uk>
Newsgroups: bionet.diagnostics
Subject: M.Sc. Applied Molecular Biology of Infectious Diseases
Date: 26 Jun 1998 02:38:52 -0700
Organization: LSHTM
Lines: 27
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MSc in the Applied Molecular Biology of Infectious Diseases

London School of Hygiene and Tropical Medicine


Applications are invited for entry to this course in September 1998.
Minimal entry requirements are of a class 2:2 degree or appropriate
training and experience.  The course provides a thorough understanding
and practical experience of molecular biology for students who wish to
use this approach in clinical diagnosis, epidemiological investigations,
or laboratory research on infectious diseases.  A high proportion of
students subsequently enter PhD programmes.

For more information and an application form contact:

The Deputy Registrar, London School of Hygiene & Tropical Medicine,
Keppel Street, London WC1E 7HT.  Telephone: +44 (0) 171 927 2239.  Fax:
+44 (0) 171 323 0638.  Email: registry@lshtm.ac.uk

Enquiries for course organiser: Email: m.miles@lshtm.ac.uk; Telephone:
+44 (0) 171 927 2249/2639; Fax: +44 (0) 171 636 8739. M. A. Miles

The School is an exempt charity dedicated to providing excellence in
teaching, learning and research for the benefit of health worldwide, and
is an equal opportunities employer



From owner-diagnostics@net.bio.net Sun Jun 28 23:00:00 1998
Path: biosci!biosci!not-for-mail
From: Pieter van Santen <santen.roemers@wxs.nl>
Newsgroups: bionet.diagnostics
Subject: The Main Metabolic Pathways
Date: 29 Jun 1998 00:47:35 -0700
Organization: World Access
Lines: 11
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Dear colleague,

If you are interested in The Main Metabolic Pathways on the Internet, visit:
http://home.wxs.nl/~pvsanten/mmp/mmp.html

Good luck Pieter






From owner-diagnostics@net.bio.net Sun Jun 28 23:00:00 1998
Path: biosci!biosci!not-for-mail
From: Cole Owen <cowen@electriciti.com>
Newsgroups: bionet.diagnostics
Subject: RNA Probes
Date: 29 Jun 1998 08:45:31 -0700
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snip . . .from Howie Rose:
>Has anybody had experience of using RNA probes for the detection of
pathogenic bacteria without an amplification system? 
------------
Isn't that the basis of the initial (and currently available) GenProbe
manufactured commercial "DNA" probe tests - going for RNA of the subject
pathogens rather than DNA?  Their combination GC/Chlamydia test has been
well accepted in clinical lab settings, along with other probe-based assays
that they make using a similar "RNA" test principle, I believe.  No
amplification is used other than the "natural" application for those
assays.  (They do have an amplifications system, but amplification is not
utilized for the subject assays.)

Cole Owen


Owen & Associates, Inc.
Consultants to the Healthcare Industry
1233 Camino Del Mar
Del Mar, California, USA

phone (vox) 619-481-5991
phone (fax) 619-481-1741
email:  cowen@electriciti.com

From owner-diagnostics@net.bio.net Sun Jun 28 23:00:00 1998
Path: biosci!biosci!not-for-mail
From: Howie Rose <hj.r@virgin.net>
Newsgroups: bionet.diagnostics
Subject: RNA Probes
Date: 29 Jun 1998 00:39:05 -0700
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Hi,

Has anybody had experience of using RNA probes for the detection of
pathogenic bacteria without an amplification system? As there are many
copies of RNA floating around a cell, I would have thought that a detection
system with the appropriate sensitivity highlight these without having to
amplify as is necessary with DNA.

Thanks
Howie



From owner-diagnostics@net.bio.net Tue Jun 30 23:00:00 1998
Path: biosci!biosci!not-for-mail
From: Robert Negm <negm@caesarsoftware.com>
Newsgroups: bionet.diagnostics
Subject: StrainMan
Date: 1 Jul 1998 01:19:08 -0700
Organization: Caesar Software, LLC
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Hello,

I am eager to receive feedback regarding our microbial database, called
StrainMan 1.0, from www.caesarsoftware.com. Can you please post your
comments about our database on our on-line forum at
http://www.caesarsoftware.com/forum_frm.htm. Feel free to post any
gripes, praise, or constructive criticisms. At Caesar Software, we are
trying to make the best microbial database ever developed. Thanks again
for everyone's support.

Sincerely,

Robert Negm, PhD
Scientific Advisor,
Caesar Software LLC
negm@caesarsoftware.com
http://www.caesarsoftware.com







