From owner-rapd@net.bio.net Wed Sep 01 01:46:00 1999
Path: biosci!ICOM.ICOM.IT!qeeriotu44
From: qeeriotu44@ICOM.ICOM.IT (covmserh)
Newsgroups: bionet.molbio.rapd
Subject: Tibetan mushroom increases lung capacity and energy.
Date: 31 Aug 1999 19:46:04 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 22
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199908312366TAA4388@leuisoe.ser.co.kr>
NNTP-Posting-Host: net.bio.net

Athletes, work-out devotees and cholesterol-compromised people take
note:  The active ingredient of a rare mushroom that grows at 14,000
feet in Tibet and was reserved only for Chinese royalty has been
synthesized.  Cordyceps sinensis has been clinically tested to improve
lung capacity and increase stamina and energy.  In most cases it will
also increase the HDL (good) cholesterol level.  No side effects.
Not sold in stores.  $24.95 for month's supply.  Also, we have
standardized green tea capsules equivalent to four cups of green tea.
One hundred times more  potent an antioxidant than vitamin C, green
tea polyphenols are the only antioxidants that penetrate the cell
membrane and protect the DNA.  Studies show they kill prostate cancer
cells (Mayo Clinic) and prevent or alleviate rheumatoid arthritis
( Proceedings of the National Academy of Sciences).  Our product has
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far.  Only $16.95 for month's supply.  For info on how to buy or sell:
email  north34@bigfoot.com   with the subject  "energy" or send a
fax to :  603-537-0753

To be deleted from the list, email north34@bigfoot.com  with the
subject line as  "remove" Have a nice day

OVER--

From owner-rapd@net.bio.net Wed Sep 01 04:20:00 1999
Path: biosci!WSUNIX.WSU.EDU!arthurr
From: arthurr@WSUNIX.WSU.EDU (art roberts)
Newsgroups: bionet.molbio.rapd
Subject: Site with many molecular biology and genetics links!!!
Date: 31 Aug 1999 22:20:19 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 45
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <37CCB670.7C9031EF@wsunix.wsu.edu>
NNTP-Posting-Host: net.bio.net

Great, innovative, and expanding site found at

http://www.biotech-resource.com


Features
--------

Bioethics/ Legal Issues - What are the ethical and legal issues in
biotechnology today?
Best sites in Biotechnology - It is a list of the Best Biotechnology
Sites in the World.
Employment opportunities - Employment opportunities in the
Biotechnology/Biology field.
Search Engine - this simple search engine allows access to all links and
the information
                in the site.
Add-A-Link - add your favorite link to my website.
Book Reviews - it is a small list of books that I thought would be of a
general interest.

This site provides a wide range of information and links for the
biochemist, biophysicist,
molecular biologist, and science educator.  There is also an extensive
list of software
resources that are free and available over the internet.  This site is
non-commercial and it
is available for your enjoyment.  I appreciate your comments and
suggestions, and I will
reply to all emails (email: arthurr@wsunix.wsu.edu).

Coming Soon
-----------
I also plan to have stock information available about biotechnology
companies in the near
future.

        Sincerely,
        Art Roberts
        (web designer)

(P.S. This site can also be accessed by http://biotech.iscool.net or
http://www.ahpcc.unm.edu/~aroberts ,
if you have trouble accessing it by http://www.biotech-resource.com .)


From owner-rapd@net.bio.net Thu Sep 02 08:58:00 1999
Path: biosci!rz.uni-jena.de!Johannes.Woestemeyer
From: Johannes.Woestemeyer@rz.uni-jena.de (Johannes Woestemeyer)
Newsgroups: bionet.molbio.rapd
Subject: Fungal Phylogeny for PhD students
Date: 2 Sep 1999 02:57:55 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 62
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <3.0.3.32.19990902114941.006c10c4@pop3.uni-jena.de>
NNTP-Posting-Host: net.bio.net

Dear colleagues!

Please forward this job offer to all those in your vicinity who could be
interested in working on molecular phylogeny of fungi: 

In a project financed by 'Deutsche Forschungsgemeinschaft' we work on
family and order structure of zygomycetes. Based on sequences of protein
coding genes from the cellular functions 'cell cycle control',
'cytoskeleton' and 'translational apparatus' we want to add the
phylogenetic dimension to a wealth of taxonomic knowledge and expertise in
this important fungal group. 

The position is to be filled beginning of October at the earliest and end
of the Winter term at the latest. Knowledge of German language is not
required. 

Experimental working conditions are good. We are technically well equipped
and have sound expertise at all levels of cloning and sequencing. Primers
for the required genes have been developed and checked in screening
experiments.  

Research is institutionally linked to an independent group at the institute
of General Microbiology and Microbial Genetics, the 'Fungal Reference
Centre' (FRC). The PhD candidate will be supervised by the FRC leader, Dr.
Kerstin Voigt and by myself in close cooperation. Both supervisors have
their experimental skills in this and other fields and perform experiments
themselves within the project.  

We expect a highly motivated young colleague, integration into a vivid
multidisciplinary institute, some expertise in Genetics and Molecular
Biology as well as a feeling for evolutionary biology. Special taxonomic
knowledge of fungi is not requested at the beginning. 

If interested, please send your details to Dr. Voigt or to me:

Friedrich-Schiller-Universitaet Jena
Lehrstuhl fuer Allgemeine Mikrobiologie und Mikrobengenetik
Neugasse 24
D-07743 Jena

Email applications are also possible: please direct to b5wojo@rz.uni-jena.de 

I will call back for further details or in order to make appointments for a
personal date, ideally beginning of October.

Best wishes,
Johannes Woestemeyer


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

Prof. Dr. Johannes Woestemeyer
Institute of General Microbiology and Microbe Genetics
Friedrich-Schiller-University Jena
Neugasse 24
D-07743 Jena - Germany
Tel.    : +49 (0)3641 949310/1
Fax     : +49 (0)3641 949312
E-Mail  : b5wojo@rz.uni-jena.de  
Homepage: http://www.uni-jena.de/biologie/mikrobio/

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

From owner-rapd@net.bio.net Thu Sep 02 09:03:00 1999
Path: biosci!rz.uni-jena.de!Johannes.Woestemeyer
From: Johannes.Woestemeyer@rz.uni-jena.de (Johannes Woestemeyer)
Newsgroups: bionet.molbio.rapd
Subject: Doktorandenstelle: Phylogenie der Pilze
Date: 2 Sep 1999 03:03:07 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 66
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <3.0.3.32.19990902115456.006c10c4@pop3.uni-jena.de>
NNTP-Posting-Host: net.bio.net

Liebe Kolleginnen und Kollegen sowie alle Interessentinnen an einer Arbeit
im Bereich Molekulare Phylogenie!


Mit der Bitte um Weitergabe an Interessierte schicke ich Ihnen die folgende
Ausschreibung:


Die DFG foerdert uns ein Projekt, in dem es um die Neubewertung der
Familien- und Ordnungsstruktur in einer grossen Gruppe von Pilzen
(Zygomyceten) geht. Anhand der Sequenzen Protein-kodierender Gene aus
'Zellzyklus-Steuerung', 'Translationsapparat' und 'Cytoskelett' soll
endlich das nicht geringe taxonomische Wissen ueber diese Pilze in einen
phylogenetischen Kontext gebracht werden.

Wir wollen die Stelle fruehestens zum 1. Oktober und (aller)spaetestens zum
Ende des Wintersemesters besetzen. Bezahlung wie ueblich nach BAT IIa/2.
Die experimentellen Voraussetzungen sind
gut, da wir fuer alle benoetigten Gene passende Primerpaare erprobt haben.
Apparativ sind wir im Hinblick auf PCR und Sequenzierung gut ausgestattet.
Experimentell-technisches know-how ist bei allen Mitarbeitern im Haus
vorhanden. Die Arbeit ist angesiedelt an einer selbstaendigen Abteilung am
Institut, dem 'Pilz-Referenz-Zentrum Jena' (PRZ), das auf der
Forschungsseite den Schwerpunkt auf der Molekularen Phylogenie der Pilze
hat. Die Arbeit wird in enger Abstimmung von mir und Dr. Kerstin Voigt als
Leiterin des PRZ betreut. Beide Betreuer/innen experimentieren auch selbst
innerhalb des Projektrahmens.

Wir erwarten von der Neuen oder dem Neuen hohe Motivation, Integration in
ein reges, wissenschaftlich vielschichtiges Institut, Vorkenntnisse in
Genetik und  Molekularbiologie, sowie ein Feeling fuer Evolutionsbiologie.
Spezielle taxonomische Kenntnisse sind erst einmal nicht erforderlich.

Wenn Sie Interesse haben, bitte ich um Ihre Bewebungsunterlagen an Dr.
Voigt oder mich unter der Adresse:

Friedrich-Schiller-Universitaet Jena
Lehrstuhl fuer Allgemeine Mikrobiologie und Mikrobengenetik
Neugasse 24
D-07743 Jena

Email-Berwerbungen an b5wojo@rz.uni-jena.de sind ebenfalls moeglich. Ich
melde mich dann bei Ihnen wegen weiterer Auskuenfte oder eines
Gespraechstermins, der im Idealfall Anfang Oktober stattfinden sollte, bei
Ihnen zurueck.

Mit freundlichem Gruss,

Joh.  Woestemeyer




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

Prof. Dr. Johannes Woestemeyer
Institute of General Microbiology and Microbe Genetics
Friedrich-Schiller-University Jena
Neugasse 24
D-07743 Jena - Germany
Tel.    : +49 (0)3641 949310/1
Fax     : +49 (0)3641 949312
E-Mail  : b5wojo@rz.uni-jena.de  
Homepage: http://www.uni-jena.de/biologie/mikrobio/

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

From owner-rapd@net.bio.net Thu Sep 02 11:00:00 1999
Path: biosci!rz.uni-jena.de!Johannes.Woestemeyer
From: Johannes.Woestemeyer@rz.uni-jena.de (Johannes Woestemeyer)
Newsgroups: bionet.molbio.rapd
Subject: Assi-Stelle in Jena: Cell cycle
Date: 2 Sep 1999 05:00:01 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 58
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <3.0.3.32.19990902135153.006d0c18@pop3.uni-jena.de>
NNTP-Posting-Host: net.bio.net

Liebe Kolleginnen,

ich bitte um Bekanntgabe der folgenden Stellenausschreibung (auch
erschienen in 'Die Zeit' vom 19. August) in Ihrem Umfeld.

Mit herzlichem Dank,
Johannes Woestemeyer



Friedrich-Schiller-Universitaet Jena

Zum naechstmoeglichen Termin, fruehestens zum 1.10.1999, ist die Stelle
eines/einer

Wissenschaftlichen Mitarbeiters/-in
am Lehrstuhl fuer Allgemeine Mikrobiologie und Mikrobengenetik zu besetzen.

Schwerpunktaufgaben: Uebernahme mikrobiologischer Grundkurse fuer den
Studiengang Diplom-Biologie; Beteiligung am Grosspraktikum im Hauptstudium
mit Schwerpunkten im Bereich Molekularbiologie und Genetik von pilzen.
Forschungsthema ist die Klonierung und Charakterisierung von
Zellcyclus-Genen endogener Mykorrhiza-Pilze. Die Einbindung in das
Schwerpunktprogramm 'Mykorrhiza' der DFG wird angestrebt. 

Qualifikation: Promotion in Biologie oder Chemie/Biochemie

Gewuenschte Expertise: Interesse fuer Pilz/Pflanze-Interaktionen; PCR- und
Klonierungskenntnisse.

Verguetung gemaess BAT-O/IIa; die Stelle ist zunaechst fuer zwei Jahre
befristet.

Bewerbungen von Frauen werden ausdruecklich begruesst. Schwerbehinderte
werden bei gleicher Eignung bevorzugt beruecksichtigt.

Bewerbungen mit vollstaendigen Bewerbungsunterlagen unter Angabe der
Reg-No. 88/99 richten Sie bitte an:

FSU Jena
Lehrstuhl fuer Allg. Mikrobiologie und Mikrobengenetik
Prof. J. Woestemeyer
Neugasse 24
D-07743 Jena

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

Prof. Dr. Johannes Woestemeyer
Institute of General Microbiology and Microbe Genetics
Friedrich-Schiller-University Jena
Neugasse 24
D-07743 Jena - Germany
Tel.    : +49 (0)3641 949310/1
Fax     : +49 (0)3641 949312
E-Mail  : b5wojo@rz.uni-jena.de  
Homepage: http://www.uni-jena.de/biologie/mikrobio/

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

From owner-rapd@net.bio.net Thu Sep 02 11:10:00 1999
Path: biosci!newshost.lanl.gov!logbridge.uoregon.edu!newsfeed.icl.net!newsfeed.icl.net!newscore.gigabell.net!newscore.ipf.de!news-fra1.dfn.de!news.man.poznan.pl!news.task.gda.pl!orion.cst.tpsa.pl!news.tpnet.pl!not-for-mail
From: "michael" <mrwojcie@key.net.pl>
Newsgroups: bionet.molbio.rapd
Subject: DNA polymerases wanted
Lines: 21
X-Newsreader: Microsoft Outlook Express 4.72.3110.1
X-MimeOLE: Produced By Microsoft MimeOLE V4.72.3110.3
Message-ID: <UJtz3.18171$Qh1.261494@news.tpnet.pl>
Date: Thu, 02 Sep 1999 12:05:08 GMT
NNTP-Posting-Host: 212.160.46.95
X-Complaints-To: abuse@tpsa.pl
X-Trace: news.tpnet.pl 936273908 212.160.46.95 (Thu, 02 Sep 1999 14:05:08 MET DST)
NNTP-Posting-Date: Thu, 02 Sep 1999 14:05:08 MET DST
Organization: TPNET - http://www.tpnet.pl

Hello,
I'm looking for polymerases, in particular, would you know of or have a
source for the following
enzymes:

1.    Pfu     DNA polymerase,
2.    Tli      DNA polymerase,
3.    Vent   DNA polymerase,
4.    T4      DNA polymerase,
5. Other    room temperature stable DNA polymerase

If you could help me, please reply to priv
mrwojcie@key.net.pl

Thank you in advance

Michael R. Wojciechowski





From owner-rapd@net.bio.net Sat Sep 04 07:53:00 1999
Path: biosci!ssivvmefhvf.alpha1.rhbnc.ac.uk!tgrffr
From: tgrffr@ssivvmefhvf.alpha1.rhbnc.ac.uk
Newsgroups: bionet.molbio.rapd
Subject: Men-Learn How You Can Greatly Improve Your Sex Life -hfibgs
Date: 4 Sep 1999 01:53:04 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 50
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <wwthuuh.pbognuaplminl@bookstore>
NNTP-Posting-Host: net.bio.net

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From owner-rapd@net.bio.net Sun Sep 05 10:53:00 1999
Path: biosci!DOLORES.SE!zejozie25
From: zejozie25@DOLORES.SE (Fine Tuning)
Newsgroups: bionet.molbio.rapd
Subject: CABLE TV  Premium Channels....No extra charge
Date: 5 Sep 1999 04:53:10 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 175
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <19990905549BAA15359@hoblyyodlydew.portquebec.ca>
NNTP-Posting-Host: net.bio.net

                   

This is really COOL!


ENHANCE Your Cable TV!

EASY to assemble plans for only $7.00 !

GET THE MOST out of your cable TV by using this 
SIMPLE "Fine Tuning" device!  YOU WILL HAVE GREAT RESULTS! 
YOU will be enjoying enhanced cable viewing in just a few days!

This Cable TV FINE TUNING DEVICE will make your 
viewing experince MUCH MORE ENJOYABLE! 

There is one problem though. It may accidentally receive stations that 
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This would include:

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 271-1325                       2.2k ohm resistor 
 278-212                        chasis connectors
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From owner-rapd@net.bio.net Sun Sep 05 16:51:00 1999
Path: biosci!BWORLD.COM.PH!listserver09
From: listserver09@BWORLD.COM.PH
Newsgroups: bionet.molbio.rapd
Subject: Don't Get Ripped Off With A $15 or $22 Program...
Date: 5 Sep 1999 10:51:19 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 211
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199909051749.AA08406@ns.hanjung.co.kr>
Reply-To: listserver09@bworld.com.ph
NNTP-Posting-Host: net.bio.net

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From owner-rapd@net.bio.net Mon Sep 06 14:49:00 1999
Path: biosci!163.NET!jiayun98
From: jiayun98@163.NET
Newsgroups: bionet.molbio.rapd
Subject: Need E.coli J5
Date: 6 Sep 1999 08:49:24 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 14
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <19990906151813.17675.fmail@163.net>
Reply-To: jiayun98@163.net
NNTP-Posting-Host: net.bio.net

Dear colleagues!
  I'm a medical student of Xijing Hospital. I need Escherichia coli J5 strain urgently in my experiments,unfortunately it is not available from our resources. 
  Could anyone give me some Escherichia coli J5 strain? Any help would be greatly appreciated!
  My email: jiayun98@163.net
  Address:  Department of Clinical Laboratory,
            Xijing Hospital, 710032
            Xi'an, China.
                                             Jiayun Liu
                                              1999.09.06

________________________________________________
»¶Ó­ÄúÊ¹ÓÃ163µç×ÓÓÊ¾ÖÃâ·Ñ·þÎñ http://www.163.net
163³¬¼¶¿áÈ«¹ú×î´óµÄÃâ·Ñ¸öÈËÖ÷Ò³»ùµØhttp://cool.163.net


From owner-rapd@net.bio.net Mon Sep 06 14:49:00 1999
Path: biosci!163.NET!jiayun98
From: jiayun98@163.NET
Newsgroups: bionet.molbio.rapd
Subject: Need E.coli J5
Date: 6 Sep 1999 08:49:08 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 14
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <19990906151756.17549.fmail@163.net>
Reply-To: jiayun98@163.net
NNTP-Posting-Host: net.bio.net

Dear colleagues!
  I'm a medical student of Xijing Hospital. I need Escherichia coli J5 strain urgently in my experiments,unfortunately it is not available from our resources. 
  Could anyone give me some Escherichia coli J5 strain? Any help would be greatly appreciated!
  My email: jiayun98@163.net
  Address:  Department of Clinical Laboratory,
            Xijing Hospital, 710032
            Xi'an, China.
                                             Jiayun Liu
                                              1999.09.06

________________________________________________
»¶Ó­ÄúÊ¹ÓÃ163µç×ÓÓÊ¾ÖÃâ·Ñ·þÎñ http://www.163.net
163³¬¼¶¿áÈ«¹ú×î´óµÄÃâ·Ñ¸öÈËÖ÷Ò³»ùµØhttp://cool.163.net


From owner-rapd@net.bio.net Tue Sep 07 01:12:00 1999
Path: biosci!GNWMAIL.COM!cybermarket
From: cybermarket@GNWMAIL.COM
Newsgroups: bionet.molbio.rapd
Subject: Home loans even if you have bad credit!
Date: 6 Sep 1999 19:12:07 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 40
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199909070219.KAA03845@ionet.net.tw>
Reply-To: dplewis@gnwmail.com
NNTP-Posting-Host: net.bio.net

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From owner-rapd@net.bio.net Thu Sep 09 01:12:00 1999
Path: biosci!TUSK.EDU!prakash
From: prakash@TUSK.EDU ("C. S. Prakash")
Newsgroups: bionet.molbio.rapd
Subject: POSITION: ICRISAT: HEAD, APPLIED GENOMICS LABORATORY
Date: 8 Sep 1999 19:11:51 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 71
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <v04003a0bb3fcc04c67db@[208.253.16.70]>
NNTP-Posting-Host: net.bio.net


POSITION: ICRISAT - HEAD, APPLIED GENOMICS LABORATORY
[CODE :  IC-02/99- C]

The International Crops Research Institute for the Semi-Arid Tropics
(ICRISAT) is a nonprofit, autonomous, scientific research and training
institute receiving support from donors through the Consultative Group for
International Agricultural Research (CGIAR). ICRISAT undertakes global
research into the improvement of six crops (sorghum, pearl millet, finger
millet, groundnut, chickpea and pigeonpea) and into resource management
technologies to alleviate rural poverty in the semi-arid tropics which is
home to one-sixth of the world's population.

ICRISAT needs a Head, Applied Genomics Laboratory  (AGL) to be based at
Patancheru, Andhra Pradesh, India, who will provide technical leadership and
innovation in indentification, testing and implementation of molecular
strategies, techniques and analyses to enhance the conservation and
utilization of crop germplasm and investigage pathogens. The Head, (AGL)
reports to the Program Director- Genetic Resources and Enhancement Program
(GREP).

The appointee will a) support curatorial needs for the Gene Bank by
describing genomic variation and monitor changes in allele frequencies; b)
strengthen genetic enhancement via gene mapping and marker identification
for assisted-selection and aided-introgression using both the wild relatives
of crop plants as well as landrace germplasm.

The appointee's specific duties include a) developing linkages and
collaborative research projects with advanced research organizations,
national agricultural research systems and universities in the semi-arid
tropics; b)  co-ordinate grant proposals jointly with other research
partners and submit them for funding; d) coordinate the operations of
laboratory to perform automated DNA sequencing and fragment analysis,
automated DNA synthesis and DNA amplification; e) coordinate DNA and RNA
extraction, genomic and cDNA library construction, data analysis,
dissemination and documentation, presentation of results in scientific
journals and at meetings; and f) train graduate students and research
fellows and supervise laboratory technical staff and students.

Applicants should have a PhD degree in Plant Biology, Plant Breeding,
Genetics or any other related field with  at least 5 years of post-doctoral
experience in molecular genetics, molecular biology or molecular breeding,
including international exposure in genetic resources or genetic enhancement
research and development.  A record of achievement with academic
publications, successful grants management and leadership abilities is
essential. Experience in effective operation of a genetic analysis
laboratory, and ability to work well with staff, visiting scientists and
students are prerequisites. International experience in
co-ordinating/conducting research, education or development programs is
desirable.  Fluency in spoken and written English is essential and knowledge
of French is desirable. Sensitivity in working in a multicultural
environment will be given priority.

ICRISAT is an equal opportunity employer and strives for staff diversity in
gender and nationality. ICRISAT Headquarters is located at Patancheru near
Hyderabad, India with regional centers and teams in Asia and Africa.  The
Center's salaries and benefits are competitive with those of other
international institutions.  Further information about ICRISAT and the CGIAR
can be obtained via the internet at <http://www.cgiar.org/icrisat or
http://www.cgiar.org. ICRISAT welcomes enquiries from persons interested in
working while on secondment.

The appointment will be initially for THREE years with the possibility of
further extension. Please send nominations or cover letter with curriculum
vitae, including contact information of three references to N.P.
Rajasekharan, Director, Human Resources, ICRISAT, Patancheru, Andhra Pradesh
502 324, India (Phone No +91-040-3296161; fax +91-040-241239 or
+91-8455-40348), email: N.Rajasekh@cgnet.com by 31 October 1999.




From owner-rapd@net.bio.net Sat Sep 11 12:46:00 1999
Path: biosci!ANDROMEDA.TECTEL.COM.MX!bolodo31
From: bolodo31@ANDROMEDA.TECTEL.COM.MX (koplosw)
Newsgroups: bionet.molbio.rapd
Subject: eLectronic mktg & software....an Internet Goldmine!
Date: 11 Sep 1999 06:45:56 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 37
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199909114085CAA15826@werseryn.polito.it>
NNTP-Posting-Host: net.bio.net

  ELECTRONIC MARKETING 

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 SUCCESSFUL ITEMS FOUND IN CYBERSPACE

 The existence of the Information Superhighway narrows down to one
 important factor; information. It's been proven repeatedly that the
 ideal cyberspace products are are books, software, computer related
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 PRODUCTION COSTS

 Regardless of the product/service, most experts agree you must be
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From owner-rapd@net.bio.net Wed Sep 15 11:55:00 1999
Path: biosci!pharma-transfer.com!lisa
From: lisa@pharma-transfer.com ("Lisa Whiting")
Newsgroups: bionet.molbio.rapd
Subject: funding opportunities
Date: 15 Sep 1999 05:55:07 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 156
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <000301beff78$0fdc3240$66654180@user2>
Reply-To: <lisa@pharma-transfer.com>
NNTP-Posting-Host: net.bio.net

The information below outlines the service that we provide to researchers
looking for funding for their projects.
If you could please indicate whether this proposal is of interest to you, it
would help.
I thank you in advance for your time and I look forward to hearing from you.

Kind Regards

Lisa


                     FUNDING OPPORTUNITIES FOR RESEARCH

Our company Ballantyne Ross Ltd. specialises in medical publishing. We
produce a journal called 'Pharma-Transfer'. This journal (and its
corresponding web-site) contain summaries of current scientific research
from all over the world that has not been published anywhere else.

We have 250 subscribing clients worldwide including Glaxo-Wellcome,
SmithKline-Beecham, Eli Lilly and Bayer, who have access to this
information, as they are actively seeking the newest projects to invest in.
They obviously have an advantage over their non-subscribing competitors, as
they are the first to be aware of the research that could lead to the
discovery of new drugs in the future.

We ask researchers to submit to us a summary (300 words) on their current
research (one abstract per project if you have several). We then publish
this in our journal and its corresponding website and we highlight this
information to our clients. If interested, the industry would contact the
researcher directly and offer funding.

The entire service we provide is free of charge and because any information
you provide is appended with your contact details, any subsequent
negotiations are between yourselves and the contacting party.

I have included information that outlines the service we provide. I hope
this information is of help and I look forward to your comments on this
proposal.

Warmest Regards

Lisa Whiting
Technology Transfer Officer
Ballantyne Ross Ltd.

Tel. 44 171 724 5444
Fax 44 171 724 2632
E-mail Lisa @Pharma-Transfer.com


                    FUNDING OPPORTUNITIES FOR RESEARCHERS

What sort of research are we looking for?

We publish a diverse range - ageing, analgesia, connective tissue,
dermatology, endocrinology/cytokines, obesity, ophthalmology, urogenital,
basic science, drug screening, support services (including bioinformatics),
cardiovascular, gastroenterology, gene therapy, growth, development,
immunology, infectious diseases, neuroscience, oncology, phytotherapeutics,
reproduction, respiratory disease, transplantation and drug delivery. It is
important to realise the medium to long-term importance of regular basic
research in biomedicine. We are not looking for a drug candidate so even if
your research is not pharmaceutical, it will still undoubtedly have
applications that may be relevant.

What can we do for you?

We specialise in medical publishing and can facilitate funding opportunities
for researchers such as yourself. We will highlight your work in our journal
and on our web-site, to pharmaceutical and biotechnology companies
worldwide. They specifically subscribe to us in order to find projects to
fund. Therefore, if they are interested in your research they would then
contact you directly; clearly a powerful mechanism for potential funds.

Why should we use your service?

We are the only publishers in the world to publish research at all stages,
from early stage to patent granted to outlicencing opportunities from
companies and institutes.
Our web-site benefits from one of the most advanced search engines ever
developed. The industries that use the web-site as their working tool, put
in key words of interest and then walk away. When a new abstract appears on
the web-site (updated daily), if it matches their search enquiry, an e-mail
will automatically be sent to them. This ensures that not only does your
research achieve instant global exposure, but also that it is targeted to
the companies most likely to offer you funding. There is no other company in
the world that uses this system.

What do I have to do?

Simply e-mail (in a word document - PC format) or fax us a short summary
(250-300 words), for each project you are seeking funding for, including the
amount of funding required, and that's it! After acknowledging receipt, we
will publish your work on the web-site within 48 hrs and in the monthly
update of our next issue.


At what stage of my research should I submit an abstract?

We publish abstracts at various stages, from early research through to more
developed projects where patents may have been filed or even granted. You
may feel you have not progressed far enough in your research to publish
anything, but even a broad-based summary of your aims will attract
industries to your work for funding opportunities.

So how much does this cost?

Nothing!!! The service we provide is FREE of charge.

How much time will this take?

We do appreciate that you are busy but we estimate this will take no more
than 25 minutes of your time, which could provide funding for your whole
project.

Could someone try to exploit the information I provide?

If your research is in the early stages or at a later stage, but you do not
wish to provide too much information, then we suggest your abstract
highlights the general aspects of your research, giving an overview as
opposed to specific details. This will therefore not jeopardize any future
patent application and will also serve to protect any delicate information
from being exploited by others.

What if I am already receiving funding?

Most of the major grant-awarding bodies have no objection to recipients
receiving supplemental funding from industry. We advise you to contact your
awarding body if you are unsure of any restrictions connected to your grant.

If I submit an abstract for your journal, I cannot write for another journal
can I?

As long as the information you provide for our journal, and any other
journal in the future is in a different format and reflects the most recent
developments in your research, publishing in our journal will not affect
publishing your work at a later stage, in another journal.

What format should my abstract be in?

We are happy to format your abstract for you with your appended contact
details.

How do I get further information?

Visit our web-site!! http://www.pharma-transfer.com

If you would like to discuss this further or submit abstracts please do not
hesitate to contact me:

Contact Person:	Lisa Whiting
Address:	Ballantyne Ross Ltd
Tel:	+44 (0)171 724 5444
Fax:	+44 (0)171 724 2632
E-mail:	lisa@pharma-transfer.com


From owner-rapd@net.bio.net Wed Sep 15 17:15:00 1999
Path: biosci!att.net!tyss
From: tyss@att.net
Newsgroups: bionet.molbio.rapd
Subject: Homeworkers needed!
Date: 15 Sep 1999 11:15:13 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 124
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <846.761756.198612@ns.bigbear.com>
NNTP-Posting-Host: net.bio.net


The information in this message is private and confidential and is intended for the addressed 
recipient only. You are receiving this special offer because your address was provided as someone 
who might be interested in receiving investment news and opportunities. If you wish to be 
excluded from any future mailings and/or not interested in the offer or you think you received it 
by an error*, simply erase this message. 

______________________________________________________


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* residents of Washington State
 
 
 
 
 
 

From owner-rapd@net.bio.net Thu Sep 16 06:24:00 1999
Path: biosci!pw.nl!hey88
From: hey88@pw.nl (byo90)
Newsgroups: bionet.molbio.rapd
Subject: Make 10K A Month, Famous Private-Eye Tells All
Date: 16 Sep 1999 00:23:56 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 106
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199909162062EAA1997@2i83wood39ij.pvnet.com.mx>
NNTP-Posting-Host: net.bio.net

Oprah, Nightline, Maria Shriver, 48 Hours, 20/20 and more have all 
interviewed this famous Private Investigator. Now, you too can make 
substantial income using Schweitzers highly sought- after SECRETS.




Thank you for your interest in our training Course! Judgment Acquisition 
& Recovery, Inc.  offers an extensive training course in "How to Collect 
Judicial Judgments".

If you are like many people, you are not even sure what a Judicial Judgment 
is and why processing Judicial Judgments can earn you very substantial 
income.
When one person or business files suit against another person or business 
and wins, then winner than has a Judicial Judgment. You are happy you won 
but you will soon find out the shocking fact: "Its now up to you to Collect 
on the Judgment". The court will not even help you. In fact, employees of 
the court are forbidden by law from telling you how to collect your judgment. Basically, the winner has a piece of paper. You must trace the loser down, find their assets; their employment, bank accounts, real estate, stocks and bonds, etc.

Very few people know how to find these assets or what to do when they are 
found. The result is that millions of Judgments are just sitting in files 
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A little over 5 1/2 years ago after more than a decade and a half of locating
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Al Schweitzer discovered this powerful wealth building opportunity. 
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"In more than 70% of the cases the winner of a Judgment never sees a dime."

Right now in the United States there is between 200 and 300 billion dollars 
of uncollected Judicial Judgment debt. For every Judgment that is paid, 5 
or more Judgments take its place.

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Matt in Bakersfield, Ca. Writes, " on my very first judgment, working a 
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After only having this course for four months, Larry S. in area code 314 
stated to us- 1 am now making $2,000.00 per week and expect this to grow 
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From the above information and actual results YOU can see why we can state
the following:

With our course you can own your own successful business. A business which 
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So, if you've ever dreamed of the financial freedom that owning your own 
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directly (between the hours of 9:00am - 5:00pm, Mountain Time)
Thank you for your time and interest.


ddm34@mailcity.com


++


From owner-rapd@net.bio.net Fri Sep 17 02:19:00 1999
Path: biosci!SMTP.NJAU.EDU.CN!zhanglei
From: zhanglei@SMTP.NJAU.EDU.CN (Zhang Lei)
Newsgroups: bionet.molbio.rapd
Subject: Can random primers be used to produce genus-specific fingerprinting?
Date: 16 Sep 1999 20:19:09 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 16
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <002c01bf00ba$ba1f6540$6ff2c3ca@nn.njau.edu.cn>
NNTP-Posting-Host: net.bio.net

Dear colleagues!
    I am a postgraduate studying in Nanjing Agriculture University of China
. I want to use RAPD to distinguish  bifidobacteria from other microbiol.
But I doubt whether RAPD primers can produce bifidobacteria genus-specific
fingerprinting .For example , if there are some fragments moved in same
distance in the fingerprinting of bifidobacteria and E.coil , these
fragments must be homogenous??

    Please forgive my poor English and any help would be greatly
appreciated!

    my mail:zhanglei@smpt.njau.edu.cn

    1999.9.17



From owner-rapd@net.bio.net Fri Sep 17 02:26:00 1999
Path: biosci!SMTP.NJAU.EDU.CN!zhanglei
From: zhanglei@SMTP.NJAU.EDU.CN (Zhang Lei)
Newsgroups: bionet.molbio.rapd
Subject: Can random primers be used to produce genus-specific fingerprinting?(my right e-mail is zhanglei@smtp.njau.edu.cn)
Date: 16 Sep 1999 20:25:57 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 16
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <003a01bf00bb$b7499380$6ff2c3ca@nn.njau.edu.cn>
NNTP-Posting-Host: net.bio.net

Dear colleagues!
    I am a postgraduate studying in Nanjing Agriculture University of China
. I want to use RAPD to distinguish  bifidobacteria from other microbiol.
But I doubt whether RAPD primers can produce bifidobacteria genus-specific
fingerprinting .For example , if there are some fragments moved in same
distance in the fingerprinting of bifidobacteria and E.coil , these
fragments must be homogenous??

    Please forgive my poor English and any help would be greatly
appreciated!

    my mail:zhanglei@smtp.njau.edu.cn 

    1999.9.17



From owner-rapd@net.bio.net Fri Sep 17 08:01:00 1999
Path: biosci!internet!biosci!not-for-mail
From: biohelp (BIOSCI Administrator)
Newsgroups: bionet.molbio.rapd
Subject: BIOSCI/bionet miniFAQ & Fundraiser
Date: 17 Sep 1999 02:00:41 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 239
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199909170900.CAA02969@net.bio.net>
NNTP-Posting-Host: net.bio.net


(LAST REVISION: 14-AUG-99)

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.
--------------------------------------------------------
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
--------------------------------------------------------------------
the UK-HGMP-Resource Centre (known as hgmp.mrc.ac.uk):
-----------------------------------------------------

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@hgmp.mrc.ac.uk.  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
   majordomo@hgmp.mrc.ac.uk.  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

   Please ask for help at biosci@hgmp.mrc.ac.uk 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.


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-rapd@net.bio.net Sat Sep 18 15:21:00 1999
Path: biosci!rz.uni-jena.de!Johannes.Woestemeyer
From: Johannes.Woestemeyer@rz.uni-jena.de (Johannes Woestemeyer)
Newsgroups: bionet.molbio.rapd
Subject: Re: Can random primers be used to produce genus-specific
  fingerprinting?
Date: 18 Sep 1999 09:21:13 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 67
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <3.0.3.32.19990918181255.006c5214@pop3.uni-jena.de>
NNTP-Posting-Host: net.bio.net

Dear colleague,

we have done a lot of research on developing taxon-specific probes based on
RAPDs for fungal plant pathogens. This works fine at the pathotype level
and at the level of species. This holds true if you don't relay on single
bands or patterns of bands, but are willing to derive sequence information
from diagnostically informative bands and procede by developing
conventional PCR primers based on this sequence information. Alternatively,
but less elegant, you may use diagnostic bands for hybridization studies.
In fungi, we had little problems with cross-hybridization. At the genus
level, there is also some chance in fungi. But looking for appropriate
primers is harder.

The situation is certainly different with the more streamlined bacteria. I
could imagine that you will have to check much more primers in order to
find something reliable. Another problem is that for most bacteria, the
species definition s much broader than for fungi. (Think about the 70%
hybridization rule!). This means that your relevant fragments must be
checked very carefuly against a collection of isolates from your taxon,
which is as large as ever possible.

Some literature for fungi:

SCHÄFER, C. & WÖSTEMEYER, J. (1992). Random primer dependent PCR
differentiates aggressive from non-aggressive isolates of the oilseed rape
pathogen Phoma lingam (Lepto sphaeria maculans). Journal of Phytopathology
136, 124-136.

BURMESTER, A. & WÖSTEMEYER, J. (1994). Variability in genome organization
of the zygomycete 	Parasitella parasitica. Current Genetics 26, 456-460.

VOIGT, K. & WÖSTEMEYER, J. (1995). The combination of Gilbert/Maxam
chemical  sequencing and the dideoxynucleotide chain termination
approach facilitates the construction of species specific PCR-primers
based on diagnostic RAPD bands. Microbiological Research  150,  373-377.


SCHLEIER, S., VOIGT, K. & WÖSTEMEYER, J. (1996). RAPD-based molecular
diagnosis of mixed fungal infections in the blackleg complex of oilseed
rape (Brassica napus): evidence for genus- and 	 species-specific sequences
in the fungal genomes. Journal of Phytopathology 145, 81-87.

VOIGT, K., SCHLEIER, S. & WÖSTEMEYER, J. (1996). Molecular diagnosis
of rape seed pathogens: An experimental strategy for the development
of taxon-specific genetic markers. In: 	 Developments in Plant Pathology
11: Diagnosis and identification of plant pathogens. (H.-W. 	 Dehne
et al., eds)  Kluwer Acad. Publishers, pp 195-198.

VOIGT, K., SCHLEIER, S. & WÖSTEMYER, J. (1998). RAPD-based molecular probes
for the blackleg fungus  Leptosphaeria maculans (Phoma lingam): evidence
for pathotype-specific sequences in the  genome. Journal of Phytopathology
146, 567-576.


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

Prof. Dr. Johannes Woestemeyer
Institute of General Microbiology and Microbe Genetics
Friedrich-Schiller-University Jena
Neugasse 24
D-07743 Jena - Germany
Tel.    : +49 (0)3641 949310/1
Fax     : +49 (0)3641 949312
E-Mail  : b5wojo@rz.uni-jena.de  
Homepage: http://www.uni-jena.de/biologie/mikrobio/

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

From owner-rapd@net.bio.net Sun Sep 19 08:53:00 1999
Path: biosci!rz.uni-jena.de!Johannes.Woestemeyer
From: Johannes.Woestemeyer@rz.uni-jena.de (Johannes Woestemeyer)
Newsgroups: bionet.molbio.rapd
Subject: Re: Can random primers be used to produce genus-specific
  fingerprinting?
Date: 19 Sep 1999 02:52:58 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 67
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <3.0.3.32.19990919114432.006c77fc@pop3.uni-jena.de>
NNTP-Posting-Host: net.bio.net

Dear colleague,

we have done a lot of research on developing taxon-specific probes based on
RAPDs for fungal plant pathogens. This works fine at the pathotype level
and at the level of species. This holds true if you don't relay on single
bands or patterns of bands, but are willing to derive sequence information
from diagnostically informative bands and procede by developing
conventional PCR primers based on this sequence information. Alternatively,
but less elegant, you may use diagnostic bands for hybridization studies.
In fungi, we had little problems with cross-hybridization. At the genus
level, there is also some chance in fungi. But looking for appropriate
primers is harder.

The situation is certainly different with the more streamlined bacteria. I
could imagine that you will have to check much more primers in order to
find something reliable. Another problem is that for most bacteria, the
species definition s much broader than for fungi. (Think about the 70%
hybridization rule!). This means that your relevant fragments must be
checked very carefuly against a collection of isolates from your taxon,
which is as large as ever possible.

Some literature for fungi:

SCHÄFER, C. & WÖSTEMEYER, J. (1992). Random primer dependent PCR
differentiates aggressive from non-aggressive isolates of the oilseed rape
pathogen Phoma lingam (Lepto sphaeria maculans). Journal of Phytopathology
136, 124-136.

BURMESTER, A. & WÖSTEMEYER, J. (1994). Variability in genome organization
of the zygomycete 	Parasitella parasitica. Current Genetics 26, 456-460.

VOIGT, K. & WÖSTEMEYER, J. (1995). The combination of Gilbert/Maxam
chemical  sequencing and the dideoxynucleotide chain termination
approach facilitates the construction of species specific PCR-primers
based on diagnostic RAPD bands. Microbiological Research  150,  373-377.


SCHLEIER, S., VOIGT, K. & WÖSTEMEYER, J. (1996). RAPD-based molecular
diagnosis of mixed fungal infections in the blackleg complex of oilseed
rape (Brassica napus): evidence for genus- and 	 species-specific sequences
in the fungal genomes. Journal of Phytopathology 145, 81-87.

VOIGT, K., SCHLEIER, S. & WÖSTEMEYER, J. (1996). Molecular diagnosis
of rape seed pathogens: An experimental strategy for the development
of taxon-specific genetic markers. In: 	 Developments in Plant Pathology
11: Diagnosis and identification of plant pathogens. (H.-W. 	 Dehne
et al., eds)  Kluwer Acad. Publishers, pp 195-198.

VOIGT, K., SCHLEIER, S. & WÖSTEMYER, J. (1998). RAPD-based molecular probes
for the blackleg fungus  Leptosphaeria maculans (Phoma lingam): evidence
for pathotype-specific sequences in the  genome. Journal of Phytopathology
146, 567-576.


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

Prof. Dr. Johannes Woestemeyer
Institute of General Microbiology and Microbe Genetics
Friedrich-Schiller-University Jena
Neugasse 24
D-07743 Jena - Germany
Tel.    : +49 (0)3641 949310/1
Fax     : +49 (0)3641 949312
E-Mail  : b5wojo@rz.uni-jena.de  
Homepage: http://www.uni-jena.de/biologie/mikrobio/

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

From owner-rapd@net.bio.net Mon Sep 20 01:48:00 1999
Path: biosci!sprint.ca!suehan
From: suehan@sprint.ca ("SUE HAN")
Newsgroups: bionet.molbio.rapd
Subject: PROTEIN EXPRESSION
Date: 19 Sep 1999 19:47:12 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 92
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <02ad01bd7fc4$144f49a0$039294d1@hqian>
NNTP-Posting-Host: net.bio.net

This is a multi-part message in MIME format.

------=_NextPart_000_02AA_01BD7F89.64CC4E40
Content-Type: text/plain;
	charset="gb2312"
Content-Transfer-Encoding: quoted-printable

Do you have too many projects and limited time? If high level protein =
expression is one of your goals, C&P Biotech is ready to help you with =
sub-cloning and protein purification in E. coli.

    1.. Sub-cloning, site-directed mutagenesis, large deletion and =
insertion mutation.
    PRICE: US$ 500.00 per sample.

    2.. Protein expression and purification based on GST or =
histidine-tag fusion.
PRICE: US$ 900.00, 5.0 mg electrophoresis pure protein is guaranteed.

Give yourself the chances to concentrate on other important projects =
with knowing that professionals are handling your expression and =
purification work.=20

NO CHARGE IF WE FAILED.

CONTACT ADDRESS:

Sue Han

C&P Biotech

3 Hampton Way

Thornhill, Ontario

Canada, L3T 5C8

Email: suehan@sprint.ca

Tel: 416 992 3089

Fax: 905 886 1898


------=_NextPart_000_02AA_01BD7F89.64CC4E40
Content-Type: text/html;
	charset="gb2312"
Content-Transfer-Encoding: quoted-printable

<!DOCTYPE HTML PUBLIC "-//W3C//DTD W3 HTML//EN">
<HTML>
<HEAD>

<META content=3Dtext/html;charset=3Dgb2312 http-equiv=3DContent-Type>
<META content=3D'"MSHTML 4.72.3110.7"' name=3DGENERATOR>
</HEAD>
<BODY bgColor=3D#ffffff>
<DIV>
<P>Do you have too many projects and limited time? If high level protein =

expression is one of your goals, C&amp;P Biotech is ready to help you =
with=20
sub-cloning and protein purification in E. coli.</P>
<OL>
    <LI>Sub-cloning, site-directed mutagenesis, large deletion and =
insertion=20
    mutation.</LI>
    <P>PRICE: US$ 500.00 per sample.</P>
    <LI>Protein expression and purification based on GST or =
histidine-tag=20
    fusion.</LI></OL>
<P>PRICE: US$ 900.00, 5.0 mg electrophoresis pure protein is =
guaranteed.</P>
<P>Give yourself the chances to concentrate on other important projects =
with=20
knowing that professionals are handling your expression and purification =
work.=20
</P>
<P>NO CHARGE IF WE FAILED.</P>
<P>CONTACT ADDRESS:</P>
<P>Sue Han</P>
<P>C&amp;P Biotech</P>
<P>3 Hampton Way</P>
<P>Thornhill, Ontario</P>
<P>Canada, L3T 5C8</P>
<P>Email: <A href=3D"mailto:cathyhan66@hotmail.com"><FONT=20
size=3D2>suehan@sprint.ca</FONT></A></P>
<P>Tel: 416 992 3089</P>
<P>Fax: 905 886 1898</P></DIV></BODY></HTML>

------=_NextPart_000_02AA_01BD7F89.64CC4E40--


From owner-rapd@net.bio.net Mon Sep 20 07:08:00 1999
Path: biosci!COMPUSERVE.COM!hyg63
From: hyg63@COMPUSERVE.COM
Newsgroups: bionet.molbio.rapd
Subject: Take Control of Your Life
Date: 20 Sep 1999 01:08:42 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 31
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199909200759.QAA09697@mail.jomon.ne.jp>
NNTP-Posting-Host: net.bio.net



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From owner-rapd@net.bio.net Tue Sep 21 20:30:00 1999
Path: biosci!ROCKETMAIL.COM!albulb
From: albulb@ROCKETMAIL.COM (alberto donayre)
Newsgroups: bionet.molbio.rapd
Subject: scoring RAPD  bands
Date: 21 Sep 1999 14:29:57 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 34
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <19990921212243.3253.rocketmail@web4.rocketmail.com>
NNTP-Posting-Host: net.bio.net

Dear Sirs:

I am trying to do quite biodiversity diagnosis in
Andean Roots  using RAPD. The band scoring is a
really trouble!!! some people in the lab can see
bands I could not. How can I calculate an error
percentage for this?
Weeks ago I finished a 100 primer screening 
but the test failed in most of the primers because
the poor RERODUCIBILITY between the 3 repetitions per
primer. Should I use all the 20 DNA samples mixed for
the screening? or choose only one, ramdomly?

Thanking in advance for the asistance,

Alberto Donayre 
Universidad San Marcos
www.unmsm.edu.pe/biologia
Lima PERU
*****personal address***************
Av. Du Petit Thouars 3841, Of.101
Lima 027
PERU
***************************************






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Get your free @yahoo.com address at http://mail.yahoo.com


From owner-rapd@net.bio.net Tue Sep 21 21:01:00 1999
Path: biosci!ROCKETMAIL.COM!albulb
From: albulb@ROCKETMAIL.COM (alberto donayre)
Newsgroups: bionet.molbio.rapd
Subject: RAPD
Date: 21 Sep 1999 15:01:29 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 32
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <19990921213532.2359.rocketmail@web1.rocketmail.com>
NNTP-Posting-Host: net.bio.net

Hi All

I recently developed a research in plant biodiversity
using RAPD. In the most of the PCR reactions the
negative control (PRIMER + water) amplified some
strange bands.
We used comercial a Taq polimerase!!!, the DNA was
dilute to 5ng/µL The water was 3dd and filtered !!!
We could not find the contaminant source we supose
the enzyme sometimes amplified over the primer in the
control . Could it be possible?

Thanking any comment

Alberto Donayre
Universidad San Marcos
www.unmsm.edu.pe/biologia
PERU
****personal address********
Av. Du Petit Thouars 3841
Of. 101
Lima 027
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From owner-rapd@net.bio.net Wed Sep 22 11:39:00 1999
Path: biosci!nunhems.com!S_van_Lier
From: S_van_Lier@nunhems.com ("Stefan van Lier")
Newsgroups: bionet.molbio.rapd
Subject: DNA Proscan
Date: 22 Sep 1999 05:39:51 -0700
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Greetings,

Does anyone have experience with the gel analysis program called pro-SCORE form the company DNA ProScan?
I would be interested in your impressions of this software. I could not receive any information from this company sofar.

The Software is for Rapid Scoring of Agricultural RFLPs and RAPDs.
The software has been optimized for high volume, high accuracy agricultural genetics labs.
It helps users read and accurately score the presence or absence of particular bands of interest on multi-lane RFLP or RAPD or AFLP 1-D images. 

Thanks in advance for your help,

Stefan van Lier
The Netherlands

Nunhems Zaden
Department Research
P.O. Box 4005
6080 AA Haelen
Telephone: +31 (0)475 599304
Telefax: +31 (0)475 591361
E-mail: S_van_Lier@nunhems.com


From owner-rapd@net.bio.net Wed Sep 22 14:49:00 1999
Path: biosci!newshost.lanl.gov!logbridge.uoregon.edu!news.nero.net!not-for-mail
From: xero33@email.NOSPAM.com (Jack)
Newsgroups: bionet.molbio.rapd
Subject: Re: scoring RAPD  bands
Date: Wed, 22 Sep 1999 15:42:31 GMT
Organization: Network for Education and Research in Oregon
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We need more information on your project design and objectives.  

RAPDs are KNOWN to have low levels of reproducibility due to the low
annelaing temperatures and small size of the primers.

One way to improve your study at the outset is to have only ONE person
score your gels to maintain the highest level of consistency.
Multiple people scoring RAPD gels is a nightmare.

- Jack -

On 21 Sep 1999 14:29:57 -0700, albulb@ROCKETMAIL.COM (alberto donayre)
wrote:

:Dear Sirs:
:
:I am trying to do quite biodiversity diagnosis in
:Andean Roots  using RAPD. The band scoring is a
:really trouble!!! some people in the lab can see
:bands I could not. How can I calculate an error
:percentage for this?
:Weeks ago I finished a 100 primer screening 
:but the test failed in most of the primers because
:the poor RERODUCIBILITY between the 3 repetitions per
:primer. Should I use all the 20 DNA samples mixed for
:the screening? or choose only one, ramdomly?
:
:Thanking in advance for the asistance,
:
:Alberto Donayre 
:Universidad San Marcos
:www.unmsm.edu.pe/biologia
:Lima PERU
:*****personal address***************
:Av. Du Petit Thouars 3841, Of.101
:Lima 027
:PERU
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From owner-rapd@net.bio.net Thu Sep 23 08:07:00 1999
Path: biosci!newshost.lanl.gov!awabi.library.ucla.edu!128.32.206.55!newsfeed.berkeley.edu!skynet.be!news.belnet.be!news.rediris.es!News.cica.es!""!no
From: "Manuel G. CLAROS" <no@spam.me>
Newsgroups: bionet.molbio.rapd
Subject: Re: RAPD
Date: Thu, 23 Sep 1999 10:50:32 +0200
Organization: C.I.C.A.
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In article <19990921213532.2359.rocketmail@web1.rocketmail.com>,
alberto donayre <albulb@ROCKETMAIL.COM> wrote:

 > We could not find the contaminant source we supose
 > the enzyme sometimes amplified over the primer in the
 > control . Could it be possible?

Have you tried to change pipettors? You can have your contamination
there

Gonzalo
claros @ uma . es

From owner-rapd@net.bio.net Thu Sep 23 11:56:00 1999
Path: biosci!PIGLET.OTAGO.AC.NZ!cei32
From: cei32@PIGLET.OTAGO.AC.NZ (koplosw)
Newsgroups: bionet.molbio.rapd
Subject: New e-leads: targeted and general internet leads
Date: 23 Sep 1999 05:55:23 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 37
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NNTP-Posting-Host: net.bio.net


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From owner-rapd@net.bio.net Thu Sep 23 14:13:00 1999
Path: biosci!SCIENCEWEEK.COM!prismx
From: prismx@SCIENCEWEEK.COM ("Science-Week")
Newsgroups: bionet.molbio.rapd
Subject: FYI - Please Post
Date: 23 Sep 1999 08:13:21 -0700
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From owner-rapd@net.bio.net Thu Sep 23 15:38:00 1999
Path: biosci!newshost.lanl.gov!awabi.library.ucla.edu!142.231.112.2!cyclone.bc.net!feed.newsfeeds.com!newsfeeds.com!newsfeed.icl.net!newsfeed.icl.net!newspeer.clara.net!news.clara.net!btnet-peer!btnet!news5-gui.server.ntli.net!ntli.net!server4.netnews.ja.net!qmw!greenwich!usenet
From: THWAITES RICHARD <trg21@greenwich.ac.uk>
Newsgroups: bionet.molbio.rapd
Subject: Re: RAPD
Date: Thu, 23 Sep 1999 17:17:31 +0100
Organization: the University of Greenwich
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alberto donayre wrote:

> Hi All
>
> I recently developed a research in plant biodiversity
> using RAPD. In the most of the PCR reactions the
> negative control (PRIMER + water) amplified some
> strange bands.
> We used comercial a Taq polimerase!!!, the DNA was
> dilute to 5ng/µL The water was 3dd and filtered !!!
> We could not find the contaminant source we supose
> the enzyme sometimes amplified over the primer in the
> control . Could it be possible?
>
> Thanking any comment
>

Dear Alberto,

A common problem I'm afraid.  We often see contaminating bands in our
RAPD controls, and they can prove quite difficult to cure.  The
contamination could be coming from any one of your reaction components.
Have you tried treating the water with UV light?  Leaving it on a
transilluminator or in a crosslinker for a few minutes is usually enough
to destroy most contaminating DNA, although make sure the container the
water is in is UV transparent of course!  Actually, you can UV treat the
whole reaction mix (except for the enzyme and template, of course) if
things get really bad.  If UV treating the water doesn't work, try using
a new stock of each of the reaction components.  Contaminating DNA can
be found in some Taqs, even commercially produced varieties, and some
manufacturers have a worse reputation than others.  Primers too can be a
possible source of contamination, although most commercially-produced
oligos are uncontaminated.

Finally, are the bands in the control the same sizes as those amplified
in your samples?  If they are, then you need to be extra careful in
setting up your RAPD reactions.  Aerosols from sample DNA can easily
spread to stocks of dNTPs, buffer etc.  One tip is to finish making the
PCR master mix and put away all of the stocks (or at least make sure the
tubes are closed) before even touching the tubes containing your
samples.  If you must touch the sample tubes before making the master
mix, then change your gloves for new ones afterwards.

Don't give up, the contamination will go away in the end.  Do let me
know how you get on.

Regards, and good luck,
Richard Thwaites
Natural Resources Institute
University of Greenwich


From owner-rapd@net.bio.net Fri Sep 24 00:17:00 1999
Path: biosci!newshost.lanl.gov!logbridge.uoregon.edu!news.indiana.edu!dewolf
From: dewolf@soybean.bio.indiana.edu (Diana E. Wolf)
Newsgroups: bionet.molbio.rapd
Subject: Re: RAPD
Date: 24 Sep 1999 01:10:56 GMT
Organization: Indiana University, Bloomington
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If the bands in your no-DNA control are not the same size as in the
reactions with samples, why should you worry about them?  Small
amounts of contaminating DNA shouldn't influence the results in the
reactions with DNA added.  I read a study in which someone wanted to
see if fungus on the leaves might be influincing their RAPD results.
They extracted pure leaf and pure fungus DNA and looked at the RAPD
banding profiles. Then they mixed the two DNAs together in different
concentrations, and looked at the RAPD banding patterns.  The
concentration of the fungus DNA had to be pretty high (relative to the
plant DNA) before it influenced the banding pattern at all.  Thus, low
levels of contamination are unlikely to influency the baning pattern
of your samples when you have put a template into the mix.  I see no
reason to worry about a bit of DNA contamination in the taq, or to
worry about bands in the no-DNA control if they don't match any of the
bands in your lanes with template.

Diana

<snip>

>
>Finally, are the bands in the control the same sizes as those amplified
>in your samples?  If they are, then you need to be extra careful in
>setting up your RAPD reactions.  Aerosols from sample DNA can easily
>spread to stocks of dNTPs, buffer etc.  One tip is to finish making the
>PCR master mix and put away all of the stocks (or at least make sure the
>tubes are closed) before even touching the tubes containing your
>samples.  If you must touch the sample tubes before making the master
>mix, then change your gloves for new ones afterwards.
>

From owner-rapd@net.bio.net Sat Sep 25 03:39:00 1999
Path: biosci!AOL.COM!new6245
From: new6245@AOL.COM
Newsgroups: bionet.molbio.rapd
Subject: Play to WIN !!!
Date: 24 Sep 1999 21:39:12 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
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Sender: daemon@net.bio.net
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From owner-rapd@net.bio.net Mon Sep 27 11:35:00 1999
Path: biosci!newshost.lanl.gov!logbridge.uoregon.edu!news.maxwell.syr.edu!tank.news.pipex.net!pipex!server1.netnews.ja.net!hgmp.mrc.ac.uk!biosci
From: crismoniz@isa.utl.pt (Cristina Oliveira)
Newsgroups: bionet.molbio.rapd
Subject: ISSR gels
Date: 27 Sep 1999 13:29:09 +0100
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Dear colleagues:
Recently we began to use ISSR in diploid plums but we have some problems

with the gels and we would be very grateful if someone could give us
some suggestions and help.
When we use non denaturing gels to separate fragments one
of two situations occur:
- If we treat the gel plates with Repel-Silane, the bands (and molecular

weight marker) appeared smeared (however if the gel is denaturing, as we

use in AFLP markers we have great results, but ISSR in denaturing gels
don't work);
- If we dry the Repel-Silane, we cannot separate the glass plates apart.

We are using 6% polyaclylamide 3M urea under non denaturing conditions
as well as using Bassan (1991) silver staining protocol.
Your help is very important for us, since we think that ISSR markers
have great potential due to its high reproducibility and multiplex
ratio.
Thanking in advance for any suggestion or advice.
Your sincerely,
Luis Goulao and Cristina Oliveira




---

From owner-rapd@net.bio.net Tue Sep 28 00:56:00 1999
Path: biosci!BIGFOOT.COM!getamoreasales1
From: getamoreasales1@BIGFOOT.COM
Newsgroups: bionet.molbio.rapd
Subject: Don't Get Left Behind!
Date: 27 Sep 1999 18:56:20 -0700
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From owner-rapd@net.bio.net Wed Sep 29 00:38:00 1999
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From: madQ <madq968@djeksta.comNOSPAM>
Newsgroups: bionet.molbio.rapd
Subject: Download Ia.n.i.!!! It's free!
Date: 26 Sep 1999 18:13:47 GMT
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From owner-rapd@net.bio.net Thu Sep 30 06:54:00 1999
Path: biosci!263.NET!deng.qw
From: deng.qw@263.NET ("deng.qw")
Newsgroups: bionet.molbio.rapd
Subject: Who can give me the article named "Identification of microorganisms using Random Primed PCR "?
Date: 30 Sep 1999 00:54:47 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 25
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 Dear colleague:

      Last week , I found an abstract in Chemical Abstracts. This is an
article named "Identification of microorganisms using Random Primed
PCR". It come from the magzine ---"Mol. Biotechnol"(the whole name is
Molecular Biotechnology ,published by Humana Press .ISSN
1073-6085):1997.8(2),139-145(ENG).  But I can't find this magzine in our
school library . It is important for me to get it . Can anyone mail it
to me ?


      Thanks a lot!

     my mail:   zhanglei@smtp.njau.edu.cn

    zhanglei

    Nanjing Agriculture University in China
    1999.9.30 PM 4:00







From owner-rapd@net.bio.net Thu Sep 30 07:40:00 1999
Path: biosci!263.NET!deng.qw
From: deng.qw@263.NET ("deng.qw")
Newsgroups: bionet.molbio.rapd
Subject: Can boiled bacteria culture be used as template DNA in RAPD directly?
Date: 30 Sep 1999 01:40:08 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 33
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <37F320EC.312830BD@263.net>
NNTP-Posting-Host: net.bio.net

I have done some research on this subject. My steps are as follows:

 1.suspending the bacteria (bifidobacteria) culture in 200ul TE(PH 8.0)

 2.using lysozyme (the ultimate concentration is 1mg/ml) to remove the
call wall of bifidobacteria at 45 degree  for 30 minutes .

 3.freezing at -20 degree for 10 minutes

 4.boiling at 100 degree for 20 minutes

 5.centrifugating right now ,get the liquid above.

6.using Rnase to get rid of RNA

7.mixing the liquid above with EB solution to calculate the
concentration of  DNA according to the brightness of the fluorescence .

But I found there is faint fluorescent . Does the genomic DNA deposit?

please help me to solve this problem,thanks a lot!!!


zhanglei
                                                               a
postgraduate of Nanjing Agricultre University in China
                                                               mail:
smtp.njau.edu.cn
                                                               99.9.30
pm 4:00




