From owner-immunology@net.bio.net Thu Oct 01 23:00:00 1998
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From: "Asher" <rubens@riviera-isp.com>
Newsgroups: bionet.immunology
Subject: Re: Brain lesions
Date: Fri, 2 Oct 1998 12:01:48 +0200
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We just sent you a message,

Please accept our best encouragements

Best regards
biocareworld




PASSAUTO a écrit dans le message
<19980929125317.10309.00003490@ng16.aol.com>...
>
>Looking for information regarding multiple brain lesions related to
autoimmune
>disorders.
>
>Any help greatly appreciated.



From owner-immunology@net.bio.net Thu Oct 01 23:00:00 1998
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From: "Asher" <rubens@riviera-isp.com>
Newsgroups: bionet.immunology
Subject: Re: Brain lesions
Date: Fri, 2 Oct 1998 11:54:49 +0200
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Good morning,dear PASSAUTO
We can really help you,  if you send us further informations, thanks to the"
TRADITIONAL CHINESE DIAGNOSTIC" and the "CHINESE  FARMACOPEE".
See our Web site: http://biocareworld-riviera.com


PASSAUTO a écrit dans le message
<19980929125317.10309.00003490@ng16.aol.com>...
>
>Looking for information regarding multiple brain lesions related to
autoimmune
>disorders.
>
>Any help greatly appreciated.



From owner-immunology@net.bio.net Thu Oct 01 23:00:00 1998
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From: fm.raaphorst@azvu.nl
Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
Subject: Re: HIV/AIDS and the Perth Group. Was:"AIDS Treatment News"...
Date: Fri, 02 Oct 1998 08:34:33 GMT
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In article <3614289A.5A26@ix.netcom.com>,
  todd33@ix.netcom.com wrote:
> Leonard Pattenden wrote:
>
> > I have shown the
> > Virology 230 papers were not about "non-isolation" or it's
> > "impossibility". It was about microvesicle contamination.
>
> Leonard, maybe you can help me with a question I've never gotten
> a good answer to.  With all this microvesicle contamination that
> comes along with "HIV" when it is purified on sucrose gradients
> (at least until recently, when a paper you know about found that
> protease treatment of the gradient fraction containing "HIV"
> could remove up to 95% of the contaminants, mostly actin), how
> did Dr Gallo generate antibodies to "HIV" in a rabbit back in
> 1984 in the _Science_ papers that made him so famous?  There is
> no information about what was used as an antigen, but I think
> it is probably safe to assume that it was density gradient
> purified material, which as one of those recent _Virology_ papers
> shows, is at best half "HIV" and half cellular proteins.  The
> coomassie stained PAGE in this paper of the gradient purified
> material is not very impressive either, as far as using this as
> an antigen -- there are proteins that run the entire gamut of
> molecular weights!
>
> How could he claim that the antibodies from the rabbit were
> specific for "HIV" given that the antigen could not possibly
> have been pure "HIV" and that apparently, at that time, no one
> had really investigated methods of trying to further purfiy
> "HIV"?
>

It doesn't matter at all whether the vaccination happens with a pure isolate
- it all depends on the selection method that's used to characterize the
resulting antibodies. Immunization with something that 'is at best half
"HIV"', and the rest consisting of cellular material from a human cell line,
will work just fine. Of course you'll generate a lot of B-cell lines
producing antibodies specific for common, cellular, proteins. But in addition
there will be B-cell lines that produce an antibody against HIV-proteins.
Even if these proteins haven't been characterized by molecular cloning, you
can identify the antibodies that recognize them. For instance, you screen the
collection of antibodies you generated against uninfected cells and infected
cells. Immunofluorescence will do the trick. Antibodies specific for common
cellular antigens will bind to both infected and uninfected cell lines.
Antibodies specific for an HIV-encoded protein, for instance the envelope
proteins, will only bind to the infected cell lines.



Frank Raaphorst

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From owner-immunology@net.bio.net Thu Oct 01 23:00:00 1998
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From: "David Smith" <pharmacon@cyberus.ca>
Newsgroups: bionet.immunology
Subject: PSA antibodies
Date: 1 Oct 1998 12:53:06 GMT
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I am looking for a source of anti-PSA antibody for use in an ELISA .

From owner-immunology@net.bio.net Thu Oct 01 23:00:00 1998
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Date: Fri, 02 Oct 1998 00:34:36 -0700
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Xref: biosci bionet.immunology:14787 bionet.molbio.hiv:4953

Serological responses of cats to feline immunodeficiency virus. 
     
Hosie MJ; Jarrett O 
Department of Veterinary Pathology, University of Glasgow, UK. 
AIDS, 1990 Mar, 4:3, 215-20 
     
The proteins of feline immunodeficiency virus (FIV) were identified 
by sodium dodecylsulphate poly-acrylamide gel electrophoresis 
(SDS-PAGE) and immunoblotting.  Purified [35S]methionine/cysteine-
labelled virus contained proteins of Mr 120, 24, 17, and 10kD, of which
the most prominent were p24 and p17, and minor components of 62, 54, 
52, 41 and 32kD. Sera from FIV-infected cats precipitated two 
glycoproteins (gp) of Mr 120kD (gp120) and 41kD (gp41) from lysates
of  [14C]glucosamine-labelled infected cells. Purified virus contained
very 
little or no detectable glycoproteins. The serological response to
individual 
viral proteins was followed in experimentally infected cats by
immunoblotting. 
Since purified virus was a poor source of gp120, a method using
FIV-infected 
cell lysates was developed. Cats produced antibodies to gp120, p55, p24
and 
p17.  (The p55 was presumed to be a precursor of p24 and p17.) Following 
infection, antibodies developed first to p24 and subsequently to p17,
p55 and 
gp120. Sera from cats infected with three separate isolates of FIV, two
from 
the UK and one from the USA, had cross-reacting antibodies to all of
these
viral proteins. The criteria for identification of seropositive cats
were 
defined. 

The minimum requirement for a positive immunoblot was antibody to gp120 
or to at least three core proteins (p55, p24 and p17). Comparison of two 
commercial enzyme-linked immunosorbent assay (ELISA) kits and 
immunoblotting indicated that false-positive results occurred as a 
result of non-specific reactions in the ELISA systems.

From owner-immunology@net.bio.net Thu Oct 01 23:00:00 1998
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From: Todd Miller <todd33@ix.netcom.com>
Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
Subject: Re: HIV/AIDS and the Perth Group. Was:"AIDS Treatment News"...
Date: Thu, 01 Oct 1998 21:12:58 -0400
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Leonard Pattenden wrote:

> I have shown the
> Virology 230 papers were not about "non-isolation" or it's
> "impossibility". It was about microvesicle contamination.

Leonard, maybe you can help me with a question I've never gotten
a good answer to.  With all this microvesicle contamination that
comes along with "HIV" when it is purified on sucrose gradients
(at least until recently, when a paper you know about found that
protease treatment of the gradient fraction containing "HIV"
could remove up to 95% of the contaminants, mostly actin), how
did Dr Gallo generate antibodies to "HIV" in a rabbit back in
1984 in the _Science_ papers that made him so famous?  There is
no information about what was used as an antigen, but I think
it is probably safe to assume that it was density gradient
purified material, which as one of those recent _Virology_ papers
shows, is at best half "HIV" and half cellular proteins.  The
coomassie stained PAGE in this paper of the gradient purified
material is not very impressive either, as far as using this as
an antigen -- there are proteins that run the entire gamut of
molecular weights!

How could he claim that the antibodies from the rabbit were 
specific for "HIV" given that the antigen could not possibly
have been pure "HIV" and that apparently, at that time, no one
had really investigated methods of trying to further purfiy
"HIV"?

Todd Miller, PhD

From owner-immunology@net.bio.net Thu Oct 01 23:00:00 1998
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From: asheat@my-dejanews.com
Newsgroups: bionet.immunology
Subject: TNF production from THP-1
Date: Fri, 02 Oct 1998 15:09:59 GMT
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Dear Members

Iam finding some difficulty in getting TNF from THP-1 after stimulating with
LPS  10 ng-10,000 ng/ml(ELISA and Bioassay). Please help me in this matter.
What might be the reason for this failure.

-----------== Posted via Deja News, The Discussion Network ==----------
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From owner-immunology@net.bio.net Thu Oct 01 23:00:00 1998
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From: "Susanne Holthausen" <susanne.holthausen@mail.sg.uunet.de>
Newsgroups: bionet.immunology
Subject: C5a und Thrombozyten
Date: Fri, 2 Oct 1998 15:13:46 +0200
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Ich beschäftige mich mit der Komplementaktivierung bei Kindern mit soliden
Tumoren während IL-2 Therapie mit Kapillarlecksyndrom.
Wer kann mir allgemein über Zusammenhänge von C5a und Thrombozyten
berichten?






From owner-immunology@net.bio.net Thu Oct 01 23:00:00 1998
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From: marnix@u.washington.edu (Marnix L. Bosch)
Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
Subject: Re: "AIDS Treatment News" online * New Issue #302 (searchable/indexed)
Date: Fri, 02 Oct 1998 14:46:51 -0700
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In article <361545cd.83282293@netnews.worldnet.att.net>,
johnburgin@worldnet.att.net wrote:


> >If you knew anything about the field that you blather on about,
> >you would know that proteases are virtually never prescribed without 
> >*2* drugs from AZT's class (nucleoside analogue reverse transcriptase
> >inhibitors) The most commonly prescribed protease-containing regimens
> >consist of AZT, 3TC, and a protease. That is one thing I have never 
> >seen any "dissident" be able to explain. If AZT is so toxic, how come
> >combining it with another drug in it's class, and a protease causes
> >death rates to drop in clinical endpoint trials?

> The short answer or the long one?  I prefer the short.  Less AZT
> combined with anything else in the PI category means less toxicity.
> Why is that so confusing?  Am I missing something, do you contend that
> the same amounts of AZT are given "with" PI "therapy" as "recommended"
> alone?  There you have it, a "dissident "explains".jb

Thanks for this testimony of ignorance. I'll give you a chance to correct
it though. Please post data showing that AZT in combo therapy is given in
lower doses than used in monotherapy. If those data show the doses are no
different, then please address the question again.

Marnix Bosch

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From: johnburgin@worldnet.att.net
Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
Subject: Re: "AIDS Treatment News" online * New Issue #302 (searchable/indexed)
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On Fri, 02 Oct 1998 14:46:51 -0700, marnix@u.washington.edu (Marnix L.
Bosch) wrote:

>In article <361545cd.83282293@netnews.worldnet.att.net>,
>johnburgin@worldnet.att.net wrote:
>
>
>> >If you knew anything about the field that you blather on about,
>> >you would know that proteases are virtually never prescribed without 
>> >*2* drugs from AZT's class (nucleoside analogue reverse transcriptase
>> >inhibitors) The most commonly prescribed protease-containing regimens
>> >consist of AZT, 3TC, and a protease. That is one thing I have never 
>> >seen any "dissident" be able to explain. If AZT is so toxic, how come
>> >combining it with another drug in it's class, and a protease causes
>> >death rates to drop in clinical endpoint trials?
>
>> The short answer or the long one?  I prefer the short.  Less AZT
>> combined with anything else in the PI category means less toxicity.
>> Why is that so confusing?  Am I missing something, do you contend that
>> the same amounts of AZT are given "with" PI "therapy" as "recommended"
>> alone?  There you have it, a "dissident "explains".jb
>
>Thanks for this testimony of ignorance. I'll give you a chance to correct
>it though. Please post data showing that AZT in combo therapy is given in
>lower doses than used in monotherapy. If those data show the doses are no
>different, then please address the question again.
Marnix,  people are living longer without the dosages of AZT as before
the era of the PI's for "AIDS" therapy.  Just check out the declining
death rates,  your choice, CDC, NIH, whatever.  Answer the question,
are AZT dosages less in combined therapy than when AZT was prescribed
alone?  Can't handle this one, Herr Marnix?  jb
>
>Marnix Bosch


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Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
Subject: Re: "AIDS Treatment News" online * New Issue #302 (searchable/indexed)
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On 1 Oct 1998 17:14:56 GMT, carlton@walleye.ccbr.umn.edu (Carlton
Hogan) wrote:

>In article <3611441e.663553911@netnews.worldnet.att.net>,
> <johnburgin@worldnet.att.net> wrote:
>>On 28 Sep 1998 16:48:29 GMT, carlton@walleye.ccbr.umn.edu (Carlton
>>Hogan) wrote:
>>
>>>In article <360c04a9.319577014@netnews.worldnet.att.net>,
>>> <johnburgin@worldnet.att.net> wrote:
>>>>On 25 Sep 1998 20:52:04 GMT, carlton@walleye.ccbr.umn.edu (Carlton
>>>>Hogan) wrote:
>>>>
>>>>>In article <360bfe32.317922269@netnews.worldnet.att.net>,
>>>>> <johnburgin@worldnet.att.net> wrote:
>>>>>>On 25 Sep 1998 16:40:29 GMT, carlton@walleye.ccbr.umn.edu (Carlton
>>>>>>Hogan) wrote:
>>>>>>
>>>>>>>>johnburgin@worldnet.att.net wrote:
>>>>>>>>
>>>>>>>>
>>>>>>>>>I have spoken to AIDS patients that I have treated
>>>>>>>>>that don't know why they are taking chemotherapy medication.  
>>>>>>>
>>>>>>>Please name a prescribed drug that is *not* chemotherapy. If you treat
>>>>>>>patients, I will eat my hat.
>>>>>>Are you hungry? Dose makes the poison, I said that before.  Aspirin,
>>>>>>is a chemotherapy drug.  Now, just be sure that our laiety isn't
>>>>>>confused, and without any Clintonesque problems with defining terms,
>>>>>>ask any person who has been through "chemotherapy" what a chemotherapy
>>>>>>drug is.  You won't need to put stars around their responses. jb
>>>>>
>>>>>No stars necessary. Sure, the poison is in the dose: enough salt
>>>>>or water can kill somebody. Yet we don't advise against salt or 
>>>>>water. I'll say it again, slowly so that you can grasp it:
>>>>>dissidents commonly use the term "chemotherapy" when talking
>>>>>about HIV antivirals specifically and intentionally to confuse 
>>>>>people by making them think that cytotoxic cancer chemotherapy 
>>>
>>>>well, imagine how confused those "people" must be when you, you dumb
>>>>ass, cannot even understand that AZT is a DNA chain terminator. 
>>>
>>>Actually, although some low-level interference may occur, and cause
>>>side-effects, AZT was initially chosen as a potential HIV therapy
>>>because it is fairly specific, with much higher viral inhibition
>>>that cellular. The data is in the AZT package insert and PDR
>>>entry. If you have contrary data, please post it.
>>>
>>>> That
>>>>was probably the most ignorant statement that you have made thus far.
>>>>>is being discussed. Although AZT was screened as a candidate 
>>>>>molecule for anti-neoplastic drugs, it failed, in great degree 
>>>>>because it was not cytotoxic enough
>>>>Oh contrare, it was cytotoxic enough to be dc'd as a chemotherapy drug
>>>>when first developed at the Detroit Cancer Foundation, 1964, Jerome
>>>>Horwitz, head of the lab,  because more lab rats DIED with AZT than
>>>>without it when treated for tumors.  I guess that's not factual enough
>>>>for you either, eh? jb
>>>
>>>In the context of anti-neoplastics, an increased death rate does
>>>*not* neccesarily reflect cytotoxicity. A higher death rate can mean
>>>dozens of thing, ranging from just an ineffective treatment, to 
>>>a wide range of toxicities that are not all cytotoxic. If you have 
>>>evidence that 1. the mice died of cytotoxic effects, and 2. the dosages
>>>were (weight adjusted) roughly equivalent to prescribed human dosages
>>>please post them.
>>>
>>>Remember: you brought up up the "poison is in the dose" argument.
>>>There are many pharaceutical compounds, and even food stuffs that 
>>>are well tolerated in humans, yet will kill laboratory rates in 
>>>high enough dosages.
>>>
>>>If there is any data that supports your claims, I am eager to see it.
>>
>>The package insert, now that's interesting.  I'm really getting
>>confused by the argument that you are presenting.  You keep trying to
>>protect the assumption that AZT is not an immune depressive chemical
>>but assert that it is not a good drug for the treatment of AIDS(Why
>>isn't it, I mean, if it's so safe and so specific?) 
>
>I never said it was totally safe. AZT is fairly toxic. But it is
>not immunesuppressive in any way that resembles AIDS. The chief 
>problem is that the virus mutates so frequently, it quickly escapes
>AZT monotherapy. However, in combination with a protease, or other 
>nucleosides, AZT can be part of a very effective, and relatively 
>enduring regimen.
>
>>.  I am, and have
>>been, asserting that AZT is a bad drug for the treatment of anything
>>except those wishing to kill every living cell in their body, which,
>>it does quite well in the proper amounts and if consumed for a long
>>enough period of time.
>
>Evidence?
>
>  Protease inhibitors do not appear to be as
>>toxic from the latest info that I have seen.
>
>If you knew anything about the field that you blather on about,
>you would know that proteases are virtually never prescribed without 
>*2* drugs from AZT's class (nucleoside analogue reverse transcriptase
>inhibitors) The most commonly prescribed protease-containing regimens
>consist of AZT, 3TC, and a protease. That is one thing I have never 
>seen any "dissident" be able to explain. If AZT is so toxic, how come
>combining it with another drug in it's class, and a protease causes
>death rates to drop in clinical endpoint trials?
The short answer or the long one?  I prefer the short.  Less AZT
combined with anything else in the PI category means less toxicity.
Why is that so confusing?  Am I missing something, do you contend that
the same amounts of AZT are given "with" PI "therapy" as "recommended"
alone?  There you have it, a "dissident "explains".jb
 There are now at least
>a dozen well-conducted, randomized trials that show that combination
>therapy reduces morbidity and mortality compared to AZT montherapy.
>
>>  Maybe if you tried
>>something a little less toxic, like a placebo, the humps and Crix
>>bellys would disappear also. 
>
>Is that a lame attempt at a personal attack?
>
>Carlton


From owner-immunology@net.bio.net Fri Oct 02 23:00:00 1998
Path: biosci!news.stanford.edu!Cabal.CESspool!bofh.vszbr.cz!howland.erols.net!panix!news.columbia.edu!ciao.cc.columbia.edu!it8
From: Ilya Trakht <it8@columbia.edu>
Newsgroups: bionet.immunology
Subject: postdoctoral at columbia university
Date: Sat, 3 Oct 1998 12:47:19 -0400
Organization: Columbia University
Lines: 23
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Postdoctoral Position available now for recent graduates trained in cell
biology, molecular biology and immunology, with interests in developing
totally human monoclonal antibodies to cancer-associated antigens and
infections agents with a potential for application in clinical medicine.
An extensive expetise in cell culture, immunoassays, immunohistochemistry,
molecular biology techniques is mostly preferred.

Interested individuals should forward Curriculum Vitae, description
research experience, brief statement of research interests and three
letters of recomendation to:

Dr. Ilya Trakht
Department of Medicine, Columbia University
650W, 168th Street, BB-1011
New York, NY 10032

E-mail: it8@columbia.edu







From owner-immunology@net.bio.net Fri Oct 02 23:00:00 1998
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From: johnburgin@worldnet.att.net
Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
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On Sat, 03 Oct 1998 12:29:21 GMT, f.raaphorst@worldonline.nl wrote:

>In article <36155a63.88553199@netnews.worldnet.att.net>,
>  johnburgin@worldnet.att.net wrote:
>> On Fri, 02 Oct 1998 14:46:51 -0700, marnix@u.washington.edu (Marnix L.
>> Bosch) wrote:
>>
>> >In article <361545cd.83282293@netnews.worldnet.att.net>,
>> >johnburgin@worldnet.att.net wrote:
>> >
>> >
>> >> >If you knew anything about the field that you blather on about,
>> >> >you would know that proteases are virtually never prescribed without
>> >> >*2* drugs from AZT's class (nucleoside analogue reverse transcriptase
>> >> >inhibitors) The most commonly prescribed protease-containing regimens
>> >> >consist of AZT, 3TC, and a protease. That is one thing I have never
>> >> >seen any "dissident" be able to explain. If AZT is so toxic, how come
>> >> >combining it with another drug in it's class, and a protease causes
>> >> >death rates to drop in clinical endpoint trials?
>> >
>> >> The short answer or the long one?  I prefer the short.  Less AZT
>> >> combined with anything else in the PI category means less toxicity.
>> >> Why is that so confusing?  Am I missing something, do you contend that
>> >> the same amounts of AZT are given "with" PI "therapy" as "recommended"
>> >> alone?  There you have it, a "dissident "explains".jb
>> >
>> >Thanks for this testimony of ignorance. I'll give you a chance to correct
>> >it though. Please post data showing that AZT in combo therapy is given in
>> >lower doses than used in monotherapy. If those data show the doses are no
>> >different, then please address the question again.
>> Marnix,  people are living longer without the dosages of AZT as before
>> the era of the PI's for "AIDS" therapy.  Just check out the declining
>> death rates,  your choice, CDC, NIH, whatever.  Answer the question,
>> are AZT dosages less in combined therapy than when AZT was prescribed
>> alone?  Can't handle this one, Herr Marnix?  jb
>
>Just answer the question jb, not this evasive stuff.
>Come on, we're waiting.
you first.  It's the same kind of question, a trap.  All you have to
do is answer "yes or no".   jb
>
>Frank Raaphorst
>
>-----------== Posted via Deja News, The Discussion Network ==----------
>http://www.dejanews.com/       Search, Read, Discuss, or Start Your Own    


From owner-immunology@net.bio.net Fri Oct 02 23:00:00 1998
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From: f.raaphorst@worldonline.nl
Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
Subject: Re: HIV/AIDS and the Perth Group. Was:"AIDS Treatment News"...
Date: Sat, 03 Oct 1998 15:56:31 GMT
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In article <361626C9.1FF8@ix.netcom.com>,
  todd33@ix.netcom.com wrote:
> fm.raaphorst@azvu.nl wrote:
> >
> > In article <3614289A.5A26@ix.netcom.com>,
> >   todd33@ix.netcom.com wrote:
>
> > > How could he claim that the antibodies from the rabbit were
> > > specific for "HIV" given that the antigen could not possibly
> > > have been pure "HIV" and that apparently, at that time, no one
> > > had really investigated methods of trying to further purfiy
> > > "HIV"?
> > >
> >
> > It doesn't matter at all whether the vaccination happens with a pure
> > isolate - it all depends on the selection method that's used to
> > characterize the resulting antibodies.
>
> There was no information about this in the Gallo papers, but I
> agree this is one way to deal with the problem.
>
> > Immunization with something that 'is at best half "HIV"', and the
> > rest consisting of cellular material from a human cell line, will
> > work just fine. Of course you'll generate a lot of B-cell lines
> > producing antibodies specific for common, cellular, proteins. But
> > in addition there will be B-cell lines that produce an antibody
> > against HIV-proteins. Even if these proteins haven't been
> > characterized by molecular cloning, you can identify the antibodies
> > that recognize them. For instance, you screen the collection of
> > antibodies you generated against uninfected cells and infected
> > cells. Immunofluorescence will do the trick. Antibodies specific
> > for common cellular antigens will bind to both infected and
> > uninfected cell lines. Antibodies specific for an HIV-encoded
> > protein, for instance the envelope proteins, will only bind to
> > the infected cell lines.
>
> This could be done, although some experiments would have to be
> performed to show that antigens unique to the infected cell line
> were truly viral, and not some endogenous protein induced by the
> experiment/infection.

Granted, but we're not talking about a single protein here. Would you really
expect an epidemic of people mounting an immunological response to a
multitude of 'self' antigens? I think the size of the response, and the
repeated isolation of typical retroviral genes and proteins points to an
infection with a retrovirus.

I guess there are also methods to use such
> Western blots preparatively, so that the antibodies binding to
> specifically induced antigens could be purified.  The following
> link shows the proteins that are purified from 2 different lines
> of infected cells (lanes B and C), compared to uninfected cells
> (lane A).  I wouldn't want the task of trying to purify polyclonal
> antibodies from a rabbit that were specific for "infected" vs
> "uninfected" cells in this situation.

Why not? It's quite simple if the pathogen has been isolated and its genes
have been cloned (which to my mind has been done). One way to screen the
antibodies would be through phage-display libraries, and even such
experiments have been done.

Gallo does show the
> blots for uninfected vs infected, but selects only serum that
> was shown to be "positive" on infected at a 1:100 dilution,
> and then instead uses a 1:500 dilution for the blots with
> infected and uninfected extracts.  Frankly, even in the original
> _Science_ paper, it is extremely difficult to see anything,
> probably because of the highly diluted antibody.
>
> http://www.virusmyth.com/aids/perthgroup/geneva/slide23.htm
>
> Thanks for your response Frank.
>
> Todd Miller

I still fail to grasp why the shortcomings of the original Gallo paper refute
the current results from independent labs all over the world.

have a good weekend,

Frank

-----------== Posted via Deja News, The Discussion Network ==----------
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From owner-immunology@net.bio.net Fri Oct 02 23:00:00 1998
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From: f.raaphorst@worldonline.nl
Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
Subject: Re: "AIDS Treatment News" online * New Issue #302 (searchable/indexed)
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In article <36155a63.88553199@netnews.worldnet.att.net>,
  johnburgin@worldnet.att.net wrote:
> On Fri, 02 Oct 1998 14:46:51 -0700, marnix@u.washington.edu (Marnix L.
> Bosch) wrote:
>
> >In article <361545cd.83282293@netnews.worldnet.att.net>,
> >johnburgin@worldnet.att.net wrote:
> >
> >
> >> >If you knew anything about the field that you blather on about,
> >> >you would know that proteases are virtually never prescribed without
> >> >*2* drugs from AZT's class (nucleoside analogue reverse transcriptase
> >> >inhibitors) The most commonly prescribed protease-containing regimens
> >> >consist of AZT, 3TC, and a protease. That is one thing I have never
> >> >seen any "dissident" be able to explain. If AZT is so toxic, how come
> >> >combining it with another drug in it's class, and a protease causes
> >> >death rates to drop in clinical endpoint trials?
> >
> >> The short answer or the long one?  I prefer the short.  Less AZT
> >> combined with anything else in the PI category means less toxicity.
> >> Why is that so confusing?  Am I missing something, do you contend that
> >> the same amounts of AZT are given "with" PI "therapy" as "recommended"
> >> alone?  There you have it, a "dissident "explains".jb
> >
> >Thanks for this testimony of ignorance. I'll give you a chance to correct
> >it though. Please post data showing that AZT in combo therapy is given in
> >lower doses than used in monotherapy. If those data show the doses are no
> >different, then please address the question again.
> Marnix,  people are living longer without the dosages of AZT as before
> the era of the PI's for "AIDS" therapy.  Just check out the declining
> death rates,  your choice, CDC, NIH, whatever.  Answer the question,
> are AZT dosages less in combined therapy than when AZT was prescribed
> alone?  Can't handle this one, Herr Marnix?  jb

Just answer the question jb, not this evasive stuff.
Come on, we're waiting.

Frank Raaphorst

-----------== Posted via Deja News, The Discussion Network ==----------
http://www.dejanews.com/       Search, Read, Discuss, or Start Your Own    

From owner-immunology@net.bio.net Fri Oct 02 23:00:00 1998
Path: biosci!agate!newsfeed.berkeley.edu!howland.erols.net!netnews.com!news.internetsat.com!not-for-mail
From: tim <tim@besancon.net>
Newsgroups: bionet.immunology
Subject: Lipid and T-cell viability
Date: Sat, 03 Oct 1998 12:40:04 +0200
Organization: ets de Franche ComtŽ
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I recently tried to recover T-lymphocytes from murine mesenteric lymph
nodes. After gently pressing organs in RPMI medium, spinning 2 mn at
3000 tr/mn, and resuspending the pellet in NaCl 0,9%, I had 100% of dead
cells. I recovered and pressed many fat tissue with the lymph nodes, so
could it have any effect on cell viability ??? (Osmotic or plasmic
membran alteration until ceramide induced apoptosis ?????????) or there
is another reason. 

Thanks for replying me.

From owner-immunology@net.bio.net Fri Oct 02 23:00:00 1998
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From: "Craig W. Reynolds" <cwr@red.com>
Newsgroups: bionet.immunology,comp.ai.genetic
Subject: Re: Simulation of an immune system
Date: Fri, 02 Oct 1998 22:09:35 -0700
Organization: Netcom
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tmarly@email.sjsu.edu wrote:
> Does anyone have heard about simulating an immune system, with insertion of a
> virus ? I found some at http://acoma.santafe.edu/sfi/research/ , but there is
> nothing about the "programming side" and results ...

Look at the work by Stephanie Forrest, et al.:

http://www.cs.unm.edu/~forrest/
http://www.cs.unm.edu/~steveah/research.html





Craig Reynolds
http://hmt.com/cwr/

From owner-immunology@net.bio.net Fri Oct 02 23:00:00 1998
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From: Ilya Trakht <it8@columbia.edu>
Newsgroups: bionet.immunology
Subject: postdoctoral position at columbia university
Date: Sat, 3 Oct 1998 12:43:24 -0400
Organization: Columbia University
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Postdoctoral Position available now for recent graduates trained in cell
biology, molecular biology and immunology, with interests in developing
totally human monoclonal antibodies to cancer-associated antigens and
infectious agents with a potential for application in clinical medicine.
An extensive expetise in cell culture, immunoassays, immunohistochemistry,
molecular biology techniques is mostly preferred.

Interested individuals should forward Curriculum Vitae, description
research experience, brief statement of research interests and three
letters of recomendation to:

Dr. Ilya Trakht
Department of Medicine, Columbia University
650W, 168th Street, BB-1011
New York, NY 10032

E-mail: it8@columbia.edu







From owner-immunology@net.bio.net Fri Oct 02 23:00:00 1998
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From: Ilya Trakht <it8@columbia.edu>
Newsgroups: bionet.immunology
Subject: staff associate position - columbia university
Date: Sat, 3 Oct 1998 12:38:31 -0400
Organization: Columbia University
Lines: 21
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Staff Associate position available to study the repertoire of human
antibodies to cancer-associated antigens and infectious agents. The
ongoing project is dealing with the development of totally human
monoclonal antibodies using hybridoma methodology and lymph tissues from
human subjects. The application of such antibodies in clinical medicine is
an ultimate goal of the project.

Position requires a degree in biological science and knowledge in this
field. Candidates with extensive experience in cell biology, molecular
biology, immunohistochemistry and immunology are encouraged to send their
curriculum vitae and three references to:

Ilya Trakht, Ph.D.
Department of Medicine, Columbia University
630 W 168 Street BB-1011
New York NY 10032

E-mail: it8@columbia.edu



From owner-immunology@net.bio.net Fri Oct 02 23:00:00 1998
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References: <6tm101$9p8$4@nnrp02.primenet.com> <6ubd93$sp9$1@news1.tc.umn.edu> <36096dc3.149849333@netnews.worldnet.att.net> <Pine.A41.3.95L.980923213817.130648C-100000@login3.isis.unc.edu> <6ue2ve$95g$1@news1.tc.umn.edu> <360acf8a.240430063@netnews.worldnet.att.net> <Pine.OSF.3.95.980925110026.3344D-100000@dingo.cc.uq.edu.au> <360bf798.316232381@netnews.worldnet.att.net> <Pine.OSF.3.95.980927131545.25508A-100000@dingo.cc.uq.edu.au> <6un1ub$7la$1@nnrp1.dejanews.com> <Pine.OSF.3.95.980928145956.30700B-100000@dingo.cc.uq.edu.au> <3614289A.5A26@ix.netcom.com> <6v236p$gls$1@nnrp1.dejanews.com> <361626C9.1FF8@ix.netcom.com> <6v5hfe$d92$1@nnrp1.dejanews.com>
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Xref: biosci bionet.immunology:14810 bionet.molbio.hiv:4972

f.raaphorst@worldonline.nl wrote:
> 
> In article <361626C9.1FF8@ix.netcom.com>,
>   todd33@ix.netcom.com wrote:
> > fm.raaphorst@azvu.nl wrote:

> > > you can identify the antibodies
> > > that recognize them. For instance, you screen the collection of
> > > antibodies you generated against uninfected cells and infected
> > > cells. Immunofluorescence will do the trick. Antibodies specific
> > > for common cellular antigens will bind to both infected and
> > > uninfected cell lines. Antibodies specific for an HIV-encoded
> > > protein, for instance the envelope proteins, will only bind to
> > > the infected cell lines.
> >
> > This could be done, although some experiments would have to be
> > performed to show that antigens unique to the infected cell line
> > were truly viral, and not some endogenous protein induced by the
> > experiment/infection.
 
Todd is a fucking idiot.

Endogenous protein induced by the experiment was
ruled out by the technique described above.

Endogenous protein induced by infection is what
has been proven.  Viral proteins are produced
within the host.  It doesn't get any more 
endogenous than that.

Your continued trolling and dancing your
incompetence and incontinent, incomplete
education from a dimestore doctorate
program reflects an ego-dystonic
condition beyond repair.

Are you sure one of your Miami hookers
hasn't infected you?

Only denial would explain your continued
disregard for the lives of others for
your self-satisfaction.

PANDOC

From owner-immunology@net.bio.net Fri Oct 02 23:00:00 1998
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From: Todd Miller <todd33@ix.netcom.com>
Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
Subject: Re: HIV/AIDS and the Perth Group. Was:"AIDS Treatment News"...
Date: Sat, 03 Oct 1998 09:29:45 -0400
Organization: ICGNetcom
Lines: 57
Message-ID: <361626C9.1FF8@ix.netcom.com>
References: <6tm101$9p8$4@nnrp02.primenet.com> <6ubd93$sp9$1@news1.tc.umn.edu> <36096dc3.149849333@netnews.worldnet.att.net> <Pine.A41.3.95L.980923213817.130648C-100000@login3.isis.unc.edu> <6ue2ve$95g$1@news1.tc.umn.edu> <360acf8a.240430063@netnews.worldnet.att.net> <Pine.OSF.3.95.980925110026.3344D-100000@dingo.cc.uq.edu.au> <360bf798.316232381@netnews.worldnet.att.net> <Pine.OSF.3.95.980927131545.25508A-100000@dingo.cc.uq.edu.au> <6un1ub$7la$1@nnrp1.dejanews.com> <Pine.OSF.3.95.980928145956.30700B-100000@dingo.cc.uq.edu.au> <3614289A.5A26@ix.netcom.com> <6v236p$gls$1@nnrp1.dejanews.com>
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Xref: biosci bionet.immunology:14801 bionet.molbio.hiv:4963

fm.raaphorst@azvu.nl wrote:
> 
> In article <3614289A.5A26@ix.netcom.com>,
>   todd33@ix.netcom.com wrote:

> > How could he claim that the antibodies from the rabbit were
> > specific for "HIV" given that the antigen could not possibly
> > have been pure "HIV" and that apparently, at that time, no one
> > had really investigated methods of trying to further purfiy
> > "HIV"?
> >
> 
> It doesn't matter at all whether the vaccination happens with a pure
> isolate - it all depends on the selection method that's used to
> characterize the resulting antibodies.

There was no information about this in the Gallo papers, but I
agree this is one way to deal with the problem.

> Immunization with something that 'is at best half "HIV"', and the
> rest consisting of cellular material from a human cell line, will
> work just fine. Of course you'll generate a lot of B-cell lines
> producing antibodies specific for common, cellular, proteins. But
> in addition there will be B-cell lines that produce an antibody
> against HIV-proteins. Even if these proteins haven't been
> characterized by molecular cloning, you can identify the antibodies
> that recognize them. For instance, you screen the collection of
> antibodies you generated against uninfected cells and infected
> cells. Immunofluorescence will do the trick. Antibodies specific
> for common cellular antigens will bind to both infected and
> uninfected cell lines. Antibodies specific for an HIV-encoded
> protein, for instance the envelope proteins, will only bind to
> the infected cell lines.

This could be done, although some experiments would have to be
performed to show that antigens unique to the infected cell line
were truly viral, and not some endogenous protein induced by the
experiment/infection.  I guess there are also methods to use such
Western blots preparatively, so that the antibodies binding to
specifically induced antigens could be purified.  The following
link shows the proteins that are purified from 2 different lines
of infected cells (lanes B and C), compared to uninfected cells
(lane A).  I wouldn't want the task of trying to purify polyclonal
antibodies from a rabbit that were specific for "infected" vs
"uninfected" cells in this situation.  Gallo does show the
blots for uninfected vs infected, but selects only serum that
was shown to be "positive" on infected at a 1:100 dilution,
and then instead uses a 1:500 dilution for the blots with
infected and uninfected extracts.  Frankly, even in the original
_Science_ paper, it is extremely difficult to see anything,
probably because of the highly diluted antibody.

http://www.virusmyth.com/aids/perthgroup/geneva/slide23.htm

Thanks for your response Frank.

Todd Miller

From owner-immunology@net.bio.net Fri Oct 02 23:00:00 1998
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From: f.raaphorst@worldonline.nl
Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
Subject: Re: "AIDS Treatment News" online * New Issue #302 (searchable/indexed)
Date: Sat, 03 Oct 1998 20:39:26 GMT
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Xref: biosci bionet.immunology:14808 bionet.molbio.hiv:4970

In article <6v5q3u$98j@sjx-ixn10.ix.netcom.com>,
  gmc0@ix.netcom.com wrote:
> johnburgin@worldnet.att.net wrote:
>

> Hey dipshit!!  Get a clue!!  The dose of AZT started at 1200 mg.  Way
> too much.  People died at that dose.  It was cut to 600 mg very
> quickly.  This was in the late 80s early 90s.  That was the
> monotherapy dose.  (300 mg probably works as well).  The reality is,
> though, people today are STILL taking 600 mg a day.  Same dose.
>
> So you're just fucking dead cold wrong and dumb as a post.  And you
> claim to be in the medical field.  Jesus.  You're the type it makes it
> easy for alternative medicine people to point to and say "my god, look
> at the doctors these days."
>
> 		George M. Carter
>
Exactly. Some example.

Frank


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From owner-immunology@net.bio.net Fri Oct 02 23:00:00 1998
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From: f.raaphorst@worldonline.nl
Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
Subject: Re: "AIDS Treatment News" online * New Issue #302 (searchable/indexed)
Date: Sat, 03 Oct 1998 20:42:58 GMT
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In article <361669aa.158010084@netnews.worldnet.att.net>,
  johnburgin@worldnet.att.net wrote:
> On Sat, 03 Oct 1998 12:29:21 GMT, f.raaphorst@worldonline.nl wrote:
>

> >Just answer the question jb, not this evasive stuff.
> >Come on, we're waiting.
> you first.  It's the same kind of question, a trap.  All you have to
> do is answer "yes or no".   jb

Me first? I wasn't asked a question. You're talking nonsense. Wonderful job
you're doing here, jb. Answer the question.


Frank

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From owner-immunology@net.bio.net Sat Oct 03 23:00:00 1998
Path: biosci!news.stanford.edu!su-news-feed2.bbnplanet.com!su-news-hub1.bbnplanet.com!news.bbnplanet.com!logbridge.uoregon.edu!news.maxwell.syr.edu!newsfeed.cwix.com!139.130.250.2!intgwpad.nntp.telstra.net!nsw.nnrp.telstra.net!nsw.nntp.telstra.net!ozemail!ozemail.com.au!ozreader
From: Gary Lum <glum@ozemail.com.au>
Newsgroups: bionet.immunology
Subject: Re: PCR based diagnostik kit for Hepatitis
Date: Sun, 04 Oct 1998 14:31:32 +0930
Organization: http://www.ozemail.com.au/~glum/Gary%20Lum%20Frames.html
Lines: 22
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To: vinsin@my-dejanews.com

vinsin@my-dejanews.com wrote:

> Please help me out in finding a suitable kit for PCR diagnosis of HBV, HCV and
> HEV.

Roche Diagnostics for HCV

Regards

Gary

--
**************************************************** 
Dr Gary Lum
Director of Pathology (and Director of Microbiology)
Royal Darwin Hospital

Microbiologists do it with culture and sensitivity
http://www.ozemail.com.au/~glum/
mailto:glum@ozemail.com.au
****************************************************


From owner-immunology@net.bio.net Sat Oct 03 23:00:00 1998
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From: gmc0@ix.netcom.com (George M. Carter)
Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
Subject: Re: "AIDS Treatment News" online * New Issue #302 (searchable/indexed)
Date: Sun, 04 Oct 1998 19:51:51 GMT
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f.raaphorst@worldonline.nl wrote:

>In article <6v5q3u$98j@sjx-ixn10.ix.netcom.com>,
>  gmc0@ix.netcom.com wrote:
>> johnburgin@worldnet.att.net wrote:
>>

>> Hey dipshit!!  Get a clue!!  The dose of AZT started at 1200 mg.  Way
>> too much.  People died at that dose.  It was cut to 600 mg very
>> quickly.  This was in the late 80s early 90s.  That was the
>> monotherapy dose.  (300 mg probably works as well).  The reality is,
>> though, people today are STILL taking 600 mg a day.  Same dose.
>>
>> So you're just fucking dead cold wrong and dumb as a post.  And you
>> claim to be in the medical field.  Jesus.  You're the type it makes it
>> easy for alternative medicine people to point to and say "my god, look
>> at the doctors these days."
>>
>> 		George M. Carter
>>
>Exactly. Some example.

Thank god they're in the minority.

George



From owner-immunology@net.bio.net Sat Oct 03 23:00:00 1998
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From: asheat@my-dejanews.com
Newsgroups: bionet.immunology
Subject: Re: X International Immunology Conference program..?
Date: Sun, 04 Oct 1998 14:28:05 GMT
Organization: Deja News - The Leader in Internet Discussion
Lines: 39
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Dear Chetan Patil,

Here is the address for the site for information regrading conference
www.afl.co.in/indtravels/confer.htm

Just come to India.
Ashutosh


In article <3612ED1B.7F4E@xcancermed.leeds.ac.uk>,
  rmrmjg@cancermed.leeds.ac.uk (Michael Gough) wrote:
> Chetan Patil wrote:
> >
> > Dear Netters,
> > I am trying to find the satellite conference speakers for the Xth
> > International Immunology Conference in India, specifically for
> > (a) the "Autoimmune disease pathogenesis and treatment" in Lucknow and
> > (b) the "Major histocompatibility complexes in Medicine" in New Delhi.
> >
> > I haven't recieved the reg. packet yet and the web site does not have
> > enough information. If anyone has this information, could they PLEASE
> > mail it to me?
> > (I need to buy my ticket to India accordingly.)
> >
> > Thank you in advance!
> >
> > regards,
> > Namrata
>
> I understand those deciding who speaks have only just received the lists
> to chose from. I know how you feel - all is in chaos as far as I can
> see.
>

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From owner-immunology@net.bio.net Sat Oct 03 23:00:00 1998
Path: biosci!news.stanford.edu!newsfeed.berkeley.edu!newshub.northeast.verio.net!news-feeds.jump.net!nntp2.dejanews.com!nnrp1.dejanews.com!not-for-mail
From: asheat@my-dejanews.com
Newsgroups: bionet.immunology
Subject: Re: X International Immunology Conference program..?
Date: Sun, 04 Oct 1998 14:22:37 GMT
Organization: Deja News - The Leader in Internet Discussion
Lines: 31
Message-ID: <6v80bd$3c5$1@nnrp1.dejanews.com>
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Hello Chetan/Namrata,

Found you in problem. I'll try my best to solve your problem in a day or so.
Today is holiday and all the program copies are with our HOD. I'll get them
for you soon. Try contacting Dr. Naik for the purpose at sitanaik@sgpgi.ac.in

See you in Lucknow or in Delhi.

Vinay

In article <36106E77.8B9050D8@stanford.edu>,
  cpatil@home.com (Chetan Patil) wrote:
> Dear Netters,
> I am trying to find the satellite conference speakers for the Xth
> International Immunology Conference in India, specifically for
> (a) the "Autoimmune disease pathogenesis and treatment" in Lucknow and
> (b) the "Major histocompatibility complexes in Medicine" in New Delhi.
>
> I haven't recieved the reg. packet yet and the web site does not have
> enough information. If anyone has this information, could they PLEASE
> mail it to me?
> (I need to buy my ticket to India accordingly.)
>
> Thank you in advance!
>
> regards,
> Namrata
>

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From owner-immunology@net.bio.net Sat Oct 03 23:00:00 1998
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From: asheat@my-dejanews.com
Newsgroups: bionet.immunology
Subject: Re: X International Immunology Conference program..?
Date: Sun, 04 Oct 1998 14:29:08 GMT
Organization: Deja News - The Leader in Internet Discussion
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Dear Namrata,

Here is the address for the site for information regrading conference
www.afl.co.in/indtravels/confer.htm

Just come to India.
Ashutosh


In article <36106E77.8B9050D8@stanford.edu>,
  cpatil@home.com (Chetan Patil) wrote:
> Dear Netters,
> I am trying to find the satellite conference speakers for the Xth
> International Immunology Conference in India, specifically for
> (a) the "Autoimmune disease pathogenesis and treatment" in Lucknow and
> (b) the "Major histocompatibility complexes in Medicine" in New Delhi.
>
> I haven't recieved the reg. packet yet and the web site does not have
> enough information. If anyone has this information, could they PLEASE
> mail it to me?
> (I need to buy my ticket to India accordingly.)
>
> Thank you in advance!
>
> regards,
> Namrata
>

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From owner-immunology@net.bio.net Sat Oct 03 23:00:00 1998
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From: vinsin@my-dejanews.com
Newsgroups: bionet.immunology
Subject: Can I have map of pCMVneo
Date: Sun, 04 Oct 1998 13:24:01 GMT
Organization: Deja News - The Leader in Internet Discussion
Lines: 12
Message-ID: <6v7stg$u46$1@nnrp1.dejanews.com>
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Dear Friends,

Can I have restriction map of pCMVneo expression vector. My study is hung for
some time due to its unavailability. Kindly help me out.

Thanking you in advance

Vinay


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From owner-immunology@net.bio.net Sat Oct 03 23:00:00 1998
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From: johnburgin@worldnet.att.net
Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
Subject: Re: "AIDS Treatment News" online * New Issue #302 (searchable/indexed)
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On Sun, 04 Oct 1998 19:51:51 GMT, gmc0@ix.netcom.com (George M.
Carter) wrote:

>f.raaphorst@worldonline.nl wrote:
>
>>In article <6v5q3u$98j@sjx-ixn10.ix.netcom.com>,
>>  gmc0@ix.netcom.com wrote:
>>> johnburgin@worldnet.att.net wrote:
>>>
>
>>> Hey dipshit!!  Get a clue!!  The dose of AZT started at 1200 mg.  Way
>>> too much.  People died at that dose.  It was cut to 600 mg very
>>> quickly.  This was in the late 80s early 90s.  That was the
>>> monotherapy dose.  (300 mg probably works as well). 
Why not use 300 then?
 The reality is,

that you still haven't answered my question.  What is the dosage with
PI's?  600?  That's 600mg too much.
>>> though, people today are STILL taking 600 mg a day.  Same dose.
>>>
>>> So you're just fucking dead cold wrong and dumb as a post. 
Now you're trying to hurt my feelings again by using your extended
vocabulary(remember, a long time ago we spoke of this, after your
maxim of 100 usable words you start using profanity).  
 And you
>>> claim to be in the medical field. 
No claim, I am, and you're not.
 Jesus.
Somehow, I don't know, it just seems like using "Jesus" so close to
the words "fucking dead" makes me believe that you're getting
frustrated.  It sounds like you're making a cry for help.
  You're the type it makes it
>>> easy for alternative medicine people to point to and say "my god, look
>>> at the doctors these days."

I totally agree.  Most of the doctors that I know who try to
intelligently defend their belief in your horseshit probably should be
practicing alternative medicine.  jb
>>>
>>> 		George M. Carter
>>>
>>Exactly. Some example.
>
>Thank god they're in the minority.
>
>George
>
>


From owner-immunology@net.bio.net Sat Oct 03 23:00:00 1998
Path: biosci!news.stanford.edu!newsfeed.berkeley.edu!news-stock.gip.net!news-peer.gip.net!news.gsl.net!gip.net!newspeer.monmouth.com!nntp2.dejanews.com!nnrp1.dejanews.com!not-for-mail
From: asheat@yahoo.com
Newsgroups: bionet.immunology
Subject: Re: X International Immunology Conference program..?
Date: Sun, 04 Oct 1998 14:19:37 GMT
Organization: Deja News - The Leader in Internet Discussion
Lines: 38
Message-ID: <6v805p$38s$1@nnrp1.dejanews.com>
References: <36106E77.8B9050D8@stanford.edu>
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Dear Chetan/Namrata,

Just saw your message in the newsgroup. I am Ph.D student at Dept. of
Immnology at SGPGIMS, Lucknow. I am sorry we dont have any site for the
conference which are going to have "Autoimmune disease pathogenesis and
treatment" in Lucknow but you can mail me up you postal address I'll send you
hard copies or I'll see if I can get in my next mail to you.

Good Luck for you abck Journey to India.

Looking forward to see you in Lucknow or in International Congress in Delhi.
Just wait for a day i'll  get you all information.

You can also mail to our Chair of the Dept. Dr. Sita Naik at
sitanaik@sgpgi.ac.in

Ashutosh
In article <36106E77.8B9050D8@stanford.edu>,
  cpatil@home.com (Chetan Patil) wrote:
> Dear Netters,
> I am trying to find the satellite conference speakers for the Xth
> International Immunology Conference in India, specifically for
> (a) the "Autoimmune disease pathogenesis and treatment" in Lucknow and
> (b) the "Major histocompatibility complexes in Medicine" in New Delhi.
>
> I haven't recieved the reg. packet yet and the web site does not have
> enough information. If anyone has this information, could they PLEASE
> mail it to me?
> (I need to buy my ticket to India accordingly.)
>
> Thank you in advance!
>
> regards,
> Namrata
>

-----------== Posted via Deja News, The Discussion Network ==----------
http://www.dejanews.com/       Search, Read, Discuss, or Start Your Own    

From owner-immunology@net.bio.net Sun Oct 04 23:00:00 1998
Path: biosci!news.stanford.edu!su-news-feed2.bbnplanet.com!su-news-hub1.bbnplanet.com!cpk-news-hub1.bbnplanet.com!news.bbnplanet.com!newshub.northeast.verio.net!ix.netcom.com!news
From: gmc0@ix.netcom.com (George M. Carter)
Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
Subject: Re: "AIDS Treatment News" online * New Issue #302 (searchable/indexed)
Date: Mon, 05 Oct 1998 15:44:55 GMT
Organization: Free Radical Enterprises
Lines: 56
Message-ID: <6vapc0$s24@sjx-ixn1.ix.netcom.com>
References: <6tm101$9p8$4@nnrp02.primenet.com> <360c04a9.319577014@netnews.worldnet.att.net> <6uoekt$e45$1@news1.tc.umn.edu> <3611441e.663553911@netnews.worldnet.att.net> <6v0dag$j5k$1@news1.tc.umn.edu> <361545cd.83282293@netnews.worldnet.att.net> <marnix-0210981446510001@fae2xx.biostat.washington.edu> <36155a63.88553199@netnews.worldnet.att.net> <6v5q3u$98j@sjx-ixn10.ix.netcom.com> <6v621u$2a8$1@nnrp1.dejanews.com> <6v8jf1$obf@dfw-ixnews5.ix.netcom.com> <3617f386.29105757@netnews.worldnet.att.net>
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johnburgin@worldnet.att.net wrote:

>On Sun, 04 Oct 1998 19:51:51 GMT, gmc0@ix.netcom.com (George M.
>Carter) wrote:

>>f.raaphorst@worldonline.nl wrote:
>>
>>>In article <6v5q3u$98j@sjx-ixn10.ix.netcom.com>,
>>>  gmc0@ix.netcom.com wrote:
>>>> johnburgin@worldnet.att.net wrote:
>>>>
>>
>>>> Hey dipshit!!  Get a clue!!  The dose of AZT started at 1200 mg.  Way
>>>> too much.  People died at that dose.  It was cut to 600 mg very
>>>> quickly.  This was in the late 80s early 90s.  That was the
>>>> monotherapy dose.  (300 mg probably works as well). 
\
>Why not use 300 then?

Good question!  But they don't.

> The reality is,

>that you still haven't answered my question.  What is the dosage with
>PI's?  600?  That's 600mg too much.

They use 600.  Can't you read??  Well, asshole, this completely
contradicts your lame assertion that people aren't dropping dead of
"AZT induced AIDS" because the dosage is less.  It's not.

>>>> though, people today are STILL taking 600 mg a day.  Same dose.
>>>>
>>>> So you're just fucking dead cold wrong and dumb as a post. 
>Now you're trying to hurt my feelings again by using your extended
>vocabulary(remember, a long time ago we spoke of this, after your
>maxim of 100 usable words you start using profanity).  

Your feelings SHOULD be hurt.  You're spreading idiocy and
misinformation that could KILL people.  You don't like my vocabulary,
well tough titties.

> And you
>>>> claim to be in the medical field. 

>No claim, I am, and you're not.

Then god help the medical community.  Say--where are you?

Now:  face it.  You fucked up big time again. As a member of the
medical community, why didn't you bother to find out that people are
taking the same (600 mg) dose of AZT?  You wouldn't have made such a
great wanking fool out of yourself.

		George M. Carter



From owner-immunology@net.bio.net Sun Oct 04 23:00:00 1998
Path: biosci!UDCF.GLA.AC.UK!gqva12
From: gqva12@UDCF.GLA.AC.UK (Dr Grant Gallagher)
Newsgroups: bionet.immunology
Subject: SECOND IL-10 WORKSHOP
Date: 5 Oct 1998 06:47:02 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
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NNTP-Posting-Host: net.bio.net

HI
this message is to inform, and invite, everyone with an interest in IL-10
to take part in the 2nd IL10-Workshop.

The 2nd IL10-Workshop will take place in MILAN from the 27th-29th May, 1999.

The WebSite is at
http://www.gla.ac.uk/IL10-Workshop

and includes details of the programme, costs, etc as well as electronic
registration and abstract submission forms.

So, if you're interested in any aspect of IL-10 or related biology, come to
Milan!!!

Grant Gallagher



From owner-immunology@net.bio.net Sun Oct 04 23:00:00 1998
Path: biosci!news.stanford.edu!newsfeed.berkeley.edu!cyclone.news.idirect.com!island.idirect.com!news1.bellglobal.com!198.235.216.4.POSTED!not-for-mail
From: "Zhixiang Wang" <zxwang@cyberbeach.net>
Newsgroups: bionet.immunology
Subject: Postdoctoral Position in Canada
Lines: 33
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Date: Mon, 05 Oct 1998 11:34:58 GMT
NNTP-Posting-Host: 207.236.41.10
NNTP-Posting-Date: Mon, 05 Oct 1998 07:34:58 EDT
Organization: Bell Solutions

A postdoc position in Molecular Cell Biology is available at Northeastern
Ontario Regional Cancer Centre in Canada. The candidate has to be well
motivated, hard working with strong background in molecular biology, cell
Biology and/or Biochemistry. The successful candidate must bave a history
of productivity.

The research in my lab is focusing on Growth Factor Receptor-Mediated
Signal Transduction and Endocytosis. The current projects, funded by NCRF,
include involvement of SH2 and SH3 containing proteins such
as Grb2, shc, GAP, PI3K and PLCr in growth factors (such as EGF
and PDGF) - induced signal transduction and receptor endocytosis (Science
272,1935-1939, 1996; Mol. Cell. Biol. 18, 590-597, 1998).

For application, please submit your C.V. and three references and their
addresses, email addresses, phone and fax numbers to:

Dr. Zhixiang Wang
Dept. of Tumor Biology
Northeastern Ontario Regional Cancer Centre
41 Ramsey Lake Road
Sudbury, Ontario P3E 5J1
Canada

Tel: (705) 522-6237 ext. 2701
Fax:(705) 523-7326









From owner-immunology@net.bio.net Sun Oct 04 23:00:00 1998
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From: holzmr01@mcrcr6.med.nyu.edu (ROBERT S. HOLZMAN)
Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
Subject: Re: HIV/AIDS and the Perth Group. Was:"AIDS Treatment News"...
Date: 3 Oct 98 18:48:23 EDT
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In article <3614289A.5A26@ix.netcom.com>, Todd Miller <todd33@ix.netcom.com> writes:
> Leonard Pattenden wrote:
> 
>> I have shown the
>> Virology 230 papers were not about "non-isolation" or it's
>> "impossibility". It was about microvesicle contamination.
> 
> Leonard, maybe you can help me with a question I've never gotten
> a good answer to.  With all this microvesicle contamination that
> comes along with "HIV" when it is purified on sucrose gradients
> (at least until recently, when a paper you know about found that
> protease treatment of the gradient fraction containing "HIV"
> could remove up to 95% of the contaminants, mostly actin), how
> did Dr Gallo generate antibodies to "HIV" in a rabbit back in
> 1984 in the _Science_ papers that made him so famous? 

It's really simple todd.  if you inject a rabbit with say, 10 ug of gp120 and
10ug of actin (say 50% contaminants in the material). the rabbit will make
antibodies to both gp120 and actin (if you put it in complete freund's
adjuvant they will also make antibodies to the dead tb bacilli it contains).

The principle you seem to be missing is you don't need pure antgens to produce
antibodies. 

Nor do you need pure antigens to measure the antibodies, although it helps.




From owner-immunology@net.bio.net Sun Oct 04 23:00:00 1998
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From: roxwhsfb@bigfoot.com
Newsgroups: bionet.immunology
Subject: Owning Your Own Adult Interent Business Is Easy
Date: 5 Oct 1998 03:05:16 GMT
Organization: Your Organization
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An unregistered version of Newsgroup AutoPoster PRO
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From owner-immunology@net.bio.net Sun Oct 04 23:00:00 1998
Path: biosci!news.stanford.edu!su-news-feed2.bbnplanet.com!su-news-hub1.bbnplanet.com!cpk-news-hub1.bbnplanet.com!news.bbnplanet.com!news-a.ais.net!ais.net!newshub.tc.umn.edu!news1.tc.umn.edu!walleye.ccbr.umn.edu!carlton
From: carlton@walleye.ccbr.umn.edu (Carlton Hogan)
Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
Subject: Re: "AIDS Treatment News" online * New Issue #302 (searchable/indexed)
Date: 5 Oct 1998 15:46:34 GMT
Organization: Department of Biostatistics, University of Minnesota
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References: <6tm101$9p8$4@nnrp02.primenet.com> <3611441e.663553911@netnews.worldnet.att.net> <6v0dag$j5k$1@news1.tc.umn.edu> <361545cd.83282293@netnews.worldnet.att.net>
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Xref: biosci bionet.immunology:14825 bionet.molbio.hiv:4981

In article <361545cd.83282293@netnews.worldnet.att.net>,
 <johnburgin@worldnet.att.net> wrote:
>>
>>  Protease inhibitors do not appear to be as
>>>toxic from the latest info that I have seen.
>>
>>If you knew anything about the field that you blather on about,
>>you would know that proteases are virtually never prescribed without 
>>*2* drugs from AZT's class (nucleoside analogue reverse transcriptase
>>inhibitors) The most commonly prescribed protease-containing regimens
>>consist of AZT, 3TC, and a protease. That is one thing I have never 
>>seen any "dissident" be able to explain. If AZT is so toxic, how come
>>combining it with another drug in it's class, and a protease causes
>>death rates to drop in clinical endpoint trials?

>The short answer or the long one?  I prefer the short.  Less AZT
>combined with anything else in the PI category means less toxicity.

That *might* make sense, if the doses used in combo with the PIs
were not exactly the same as used in monotherapy.

>Why is that so confusing?  Am I missing something, do you contend that
>the same amounts of AZT are given "with" PI "therapy" as "recommended"
>alone?  There you have it, a "dissident "explains".jb

That is the fact. Before you jump in to the fray, learn the basics.

Carlton

From owner-immunology@net.bio.net Sun Oct 04 23:00:00 1998
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From: johnburgin@worldnet.att.net
Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
Subject: Re: "AIDS Treatment News" online * New Issue #302 (searchable/indexed)
Date: 5 Oct 1998 21:46:52 GMT
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On 5 Oct 1998 15:54:20 GMT, carlton@walleye.ccbr.umn.edu (Carlton
Hogan) wrote:

>In article <3617f386.29105757@netnews.worldnet.att.net>,
> <johnburgin@worldnet.att.net> wrote:
>>On Sun, 04 Oct 1998 19:51:51 GMT, gmc0@ix.netcom.com (George M.
>>Carter) wrote:
>>
>>>f.raaphorst@worldonline.nl wrote:
>>>
>>>>In article <6v5q3u$98j@sjx-ixn10.ix.netcom.com>,
>>>>  gmc0@ix.netcom.com wrote:
>>>>> johnburgin@worldnet.att.net wrote:
>>>>>
>>>
>>>>> Hey dipshit!!  Get a clue!!  The dose of AZT started at 1200 mg.  Way
>>>>> too much.  People died at that dose.  It was cut to 600 mg very
>>>>> quickly.  This was in the late 80s early 90s.  That was the
>>>>> monotherapy dose.  (300 mg probably works as well). 
>
>>Why not use 300 then?
>
>Because of resistance concerns: in vitro work suggests that "trough" levels
> are too low to guarantee continued suppression, although there 
>has not ben clinical endpoint trials over a long enough duration 
>to confirm it.
>
>> The reality is,
>>
>>that you still haven't answered my question.  What is the dosage with
>>PI's?  600?  That's 600mg too much.
>
>OK, let's take this thread back to it's beginning. I have answered your 
>question. Now you explain why, if AZT is so toxic and non-beneficial,
>is a survival benefit seen for AZT + *another* nuke + PI?
>Put up or shut up.
I don't have to do any such thing.  Remember, this is the internet,
cyberspace, we, all of us, can have and express an opinion.  You were
given a nice diatribe by Todd Miller, whom you readily dismissed as
les incompetent.  Why should I expect any different treatment from
you.  Not all are seeing the "survival benefit" from AZT +*another*
nuke + PI.  That's still up for debate.  
>
>Carlton


From owner-immunology@net.bio.net Sun Oct 04 23:00:00 1998
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From: ateasd5941@aol.com (ATeasd5941)
Newsgroups: bionet.immunology
Subject: How Far Does Medicine Go, whose Servant has It Become?
Lines: 31
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When the things that make us unique individuals become
 treatable with pills, where does the new and real sickness
 lie?

If you read, how many times will you have read, 
          " S/he was painfully shy"  ?

Any pain we suffer, in what ever form, helps us to develop
our own self consciousness. It's our consciousness of
life that forms the very essence of our existence. It is
the essence of life in your children, your family, your friends
 and fellow beings that you learn to love. Is it not for the love
of another person that man will die? Without this do we become
 no better than animals without feeling?

If you are a doctor reading this, what have your consciousness’
been treated with, that your voices are so silent on this matter?

How Far Does Medicine Go, whose Servant has It Become?
Does it serve people or does it serve the money makers?

What ' IS' at the route of all evil if the latter is the case? 

I am not saying don't treat pain, I'm saying have the wisdom to
know when pain is a part of humanity.

Think about it!

Carol T

From owner-immunology@net.bio.net Sun Oct 04 23:00:00 1998
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From: johnburgin@worldnet.att.net
Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
Subject: Re: "AIDS Treatment News" online * New Issue #302 (searchable/indexed)
Date: 5 Oct 1998 21:50:21 GMT
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On 5 Oct 1998 15:46:34 GMT, carlton@walleye.ccbr.umn.edu (Carlton
Hogan) wrote:

>In article <361545cd.83282293@netnews.worldnet.att.net>,
> <johnburgin@worldnet.att.net> wrote:
>>>
>>>  Protease inhibitors do not appear to be as
>>>>toxic from the latest info that I have seen.
>>>
>>>If you knew anything about the field that you blather on about,
>>>you would know that proteases are virtually never prescribed without 
>>>*2* drugs from AZT's class (nucleoside analogue reverse transcriptase
>>>inhibitors) The most commonly prescribed protease-containing regimens
>>>consist of AZT, 3TC, and a protease. That is one thing I have never 
>>>seen any "dissident" be able to explain. If AZT is so toxic, how come
>>>combining it with another drug in it's class, and a protease causes
>>>death rates to drop in clinical endpoint trials?
>
>>The short answer or the long one?  I prefer the short.  Less AZT
>>combined with anything else in the PI category means less toxicity.
>
>That *might* make sense, if the doses used in combo with the PIs
>were not exactly the same as used in monotherapy.
>
>>Why is that so confusing?  Am I missing something, do you contend that
>>the same amounts of AZT are given "with" PI "therapy" as "recommended"
>>alone?  There you have it, a "dissident "explains".jb
>
>That is the fact. Before you jump in to the fray, learn the basics.

Basically, as you wish to return to, I have not jumped into anything,
except apparently your face.  I believe that the past history of
Wellcome's misbehavior, and Gallo should be enough to make any
information that you provide concerning AZT and/or HIV suspect.  If
the basics are flawed, which I BELIEVE that they are, the rest should
and must be.  You're a data miner.  Need me to explain that one?  jb
>
>Carlton


From owner-immunology@net.bio.net Sun Oct 04 23:00:00 1998
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From: carlton@walleye.ccbr.umn.edu (Carlton Hogan)
Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
Subject: Re: "AIDS Treatment News" online * New Issue #302 (searchable/indexed)
Date: 5 Oct 1998 15:49:36 GMT
Organization: Department of Biostatistics, University of Minnesota
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In article <361669aa.158010084@netnews.worldnet.att.net>,
 <johnburgin@worldnet.att.net> wrote:
>On Sat, 03 Oct 1998 12:29:21 GMT, f.raaphorst@worldonline.nl wrote:
>
>>> >> The short answer or the long one?  I prefer the short.  Less AZT
>>> >> combined with anything else in the PI category means less toxicity.
>>> >> Why is that so confusing?  Am I missing something, do you contend that
>>> >> the same amounts of AZT are given "with" PI "therapy" as "recommended"
>>> >> alone?  There you have it, a "dissident "explains".jb
>>> >
>>> >Thanks for this testimony of ignorance. I'll give you a chance to correct
>>> >it though. Please post data showing that AZT in combo therapy is given in
>>> >lower doses than used in monotherapy. If those data show the doses are no
>>> >different, then please address the question again.

>>> Marnix,  people are living longer without the dosages of AZT as before
>>> the era of the PI's for "AIDS" therapy.  Just check out the declining
>>> death rates,  your choice, CDC, NIH, whatever.  Answer the question,
>>> are AZT dosages less in combined therapy than when AZT was prescribed
>>> alone?  Can't handle this one, Herr Marnix?  jb
>>
>>Just answer the question jb, not this evasive stuff.
>>Come on, we're waiting.
>you first.  It's the same kind of question, a trap.  All you have to
>do is answer "yes or no".   jb

The answer is "no", AZT is not generally prescribed in reduced dosage
with PIs. FDA approval, package inserts, and "expert panels", like
the IoMs and the IAS's all concur. Come back when you know something.

Carlton

From owner-immunology@net.bio.net Sun Oct 04 23:00:00 1998
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From: carlton@walleye.ccbr.umn.edu (Carlton Hogan)
Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
Subject: Re: "AIDS Treatment News" online * New Issue #302 (searchable/indexed)
Date: 5 Oct 1998 15:54:20 GMT
Organization: Department of Biostatistics, University of Minnesota
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In article <3617f386.29105757@netnews.worldnet.att.net>,
 <johnburgin@worldnet.att.net> wrote:
>On Sun, 04 Oct 1998 19:51:51 GMT, gmc0@ix.netcom.com (George M.
>Carter) wrote:
>
>>f.raaphorst@worldonline.nl wrote:
>>
>>>In article <6v5q3u$98j@sjx-ixn10.ix.netcom.com>,
>>>  gmc0@ix.netcom.com wrote:
>>>> johnburgin@worldnet.att.net wrote:
>>>>
>>
>>>> Hey dipshit!!  Get a clue!!  The dose of AZT started at 1200 mg.  Way
>>>> too much.  People died at that dose.  It was cut to 600 mg very
>>>> quickly.  This was in the late 80s early 90s.  That was the
>>>> monotherapy dose.  (300 mg probably works as well). 

>Why not use 300 then?

Because of resistance concerns: in vitro work suggests that "trough" levels
 are too low to guarantee continued suppression, although there 
has not ben clinical endpoint trials over a long enough duration 
to confirm it.

> The reality is,
>
>that you still haven't answered my question.  What is the dosage with
>PI's?  600?  That's 600mg too much.

OK, let's take this thread back to it's beginning. I have answered your 
question. Now you explain why, if AZT is so toxic and non-beneficial,
is a survival benefit seen for AZT + *another* nuke + PI?
Put up or shut up.

Carlton

From owner-immunology@net.bio.net Sun Oct 04 23:00:00 1998
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From: johnburgin@worldnet.att.net
Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
Subject: Re: "AIDS Treatment News" online * New Issue #302 (searchable/indexed)
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On Mon, 05 Oct 1998 15:44:55 GMT, gmc0@ix.netcom.com (George M.
Carter) wrote:

>johnburgin@worldnet.att.net wrote:
>
>>On Sun, 04 Oct 1998 19:51:51 GMT, gmc0@ix.netcom.com (George M.
>>Carter) wrote:
>
>>>f.raaphorst@worldonline.nl wrote:
>>>
>>>>In article <6v5q3u$98j@sjx-ixn10.ix.netcom.com>,
>>>>  gmc0@ix.netcom.com wrote:
>>>>> johnburgin@worldnet.att.net wrote:
>>>>>
>>>
>>>>> Hey dipshit!!  Get a clue!!  The dose of AZT started at 1200 mg.  Way
>>>>> too much.  People died at that dose.  It was cut to 600 mg very
>>>>> quickly.  This was in the late 80s early 90s.  That was the
>>>>> monotherapy dose.  (300 mg probably works as well). 
>\
>>Why not use 300 then?
>
>Good question!  But they don't.
>
>> The reality is,
>
>>that you still haven't answered my question.  What is the dosage with
>>PI's?  600?  That's 600mg too much.
>
>They use 600.  Can't you read??  Well, asshole, this completely
>contradicts your lame assertion that people aren't dropping dead of
>"AZT induced AIDS" because the dosage is less.  It's not.
And who says they're not dropping dead a little slower, which is my
contention?  Who can tell the difference between a slow death with AZT
and PI's and AIDS?  Why do you keep defending a bad drug?
>
>>>>> though, people today are STILL taking 600 mg a day.  Same dose.
>>>>>
>>>>> So you're just fucking dead cold wrong and dumb as a post. 
>>Now you're trying to hurt my feelings again by using your extended
>>vocabulary(remember, a long time ago we spoke of this, after your
>>maxim of 100 usable words you start using profanity).  
>
>Your feelings SHOULD be hurt.  You're spreading idiocy and
>misinformation that could KILL people.  You don't like my vocabulary,
>well tough titties.
Now you're telling me how I should feel.  Boy, that's really getting
low.  My "misinformation" will only cause people to read more about
alternatives that they have not explored.  If they at the very least
look into HEAL, they will do nothing more to themselves than have
another viewpoint.  If they start with your lunacy, jumping on the
drugs, they'll be sick or dead in most cases depending on who is still
recommending AZT, like you.
>
>> And you
>>>>> claim to be in the medical field. 
>
>>No claim, I am, and you're not.
>
>Then god help the medical community.  Say--where are you?
>
>Now:  face it.  You fucked up big time again. As a member of the
>medical community, why didn't you bother to find out that people are
>taking the same (600 mg) dose of AZT?  You wouldn't have made such a
>great wanking fool out of yourself.
George, a "wanking" fool?  Not in my dictionary.  I still repeat,
600mg is 600 too much without supportive data, which is still wanking.
jb
>
>		George M. Carter
>
>


From owner-immunology@net.bio.net Mon Oct 05 23:00:00 1998
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ROBERT S. HOLZMAN wrote:

> The principle you seem to be missing is you don't need pure antgens to produce
> antibodies.
> 
> Nor do you need pure antigens to measure the antibodies, although it helps.

When talking to todd or other recalcitrant nincompoops, you should
probably speak in purified yiddish...

Rabbidoc

From owner-immunology@net.bio.net Mon Oct 05 23:00:00 1998
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From: carlton@walleye.ccbr.umn.edu (Carlton Hogan)
Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
Subject: Re: "AIDS Treatment News" online * New Issue #302 (searchable/indexed)
Date: 6 Oct 1998 18:35:42 GMT
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In article <36193c02.113210495@netnews.worldnet.att.net>,
 <johnburgin@worldnet.att.net> wrote:
>On Mon, 05 Oct 1998 15:44:55 GMT, gmc0@ix.netcom.com (George M.
>Carter) wrote:

(snip)>
>>> The reality is,
>>
>>>that you still haven't answered my question.  What is the dosage with
>>>PI's?  600?  That's 600mg too much.
>>
>>They use 600.  Can't you read??  Well, asshole, this completely
>>contradicts your lame assertion that people aren't dropping dead of
>>"AZT induced AIDS" because the dosage is less.  It's not.

>And who says they're not dropping dead a little slower, which is my
>contention?  Who can tell the difference between a slow death with AZT
>and PI's and AIDS?  Why do you keep defending a bad drug?

You still haven't explain why there is marked survival benefit for
AZT in combination with ANOTHER nuke + PI compared to AZT alone.
If AZT and AZT-like drugs were so toxic, we would expect the exact 
opposite.
(Snip)
>>
>>Now:  face it.  You fucked up big time again. As a member of the
>>medical community, why didn't you bother to find out that people are
>>taking the same (600 mg) dose of AZT?  You wouldn't have made such a
>>great wanking fool out of yourself.
>George, a "wanking" fool?  Not in my dictionary.  I still repeat,
>600mg is 600 too much without supportive data, which is still wanking.

OK. You claim that the supporting data is not there. Please then offer
meaningful and detailed criticisms of ACTG 320, Abbott 047, the 
CAESAR trial, and the original Erons et al AZT+3tc study. These 
are but a few in the literally dozens of trials looking at combination 
nukes. While you are at it, howabout EACG 017, and the VA cooperative
trial? You claim that there is no supporting data: I claim that 
you are not even minimally familiar with the literature.
If you feel these trials are in error, please list specific flaws,
not just the fact that they contradict your preconceptions.

Carlton
 
 __________________________________________________________________________
 |                                                                        |
 |   Carlton Hogan  (carlton@gopher.ccbr.umn.edu)                         |
 |   Community Programs for Clinical Research on AIDS Statistical Center  |
 |   Coordinating Center for Biometric Research                           |
 |   Division of Biostatistics, School of Public Health                   |
 |   University of Minnesota          http://www.biostat.umn.edu/~carlton |
 |   2221 University Ave SE, Suite 200              Voice: (612) 626 8899 |
 |   Minneapolis  MN 55414                            FAX: (612) 626 8892 |
 |________________________________________________________________________|
   Affilation provided for purpose of identification, not representation.
   

From owner-immunology@net.bio.net Mon Oct 05 23:00:00 1998
Path: biosci!biosci!not-for-mail
From: Ilya Trakht <it8@columbia.edu>
Newsgroups: bionet.immunology
Subject: Postdoctoral Position - Columbia University
Date: 6 Oct 1998 11:37:23 -0700
Organization: Columbia University
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Postdoctoral Position available now for recent graduates trained in cell
biology, molecular biology and immunology, with interests in developing
totally human monoclonal antibodies to cancer-associated antigens and
infectious agents with a potential for application in clinical medicine.
An extensive expetise in cell culture, immunoassays, immunohistochemistry,
molecular biology techniques is mostly preferred.

Interested individuals should forward Curriculum Vitae, description
research experience, brief statement of research interests and three
letters of recomendation to:

Dr. Ilya Trakht
Department of Medicine, Columbia University
650W, 168th Street, BB-1011
New York, NY 10032

E-mail: it8@columbia.edu








From owner-immunology@net.bio.net Mon Oct 05 23:00:00 1998
Path: biosci!PANGAEA-PHARM.COM!gcole
From: gcole@PANGAEA-PHARM.COM (Geoffery Cole)
Newsgroups: bionet.immunology
Subject: x-, versus gamma-irradiation to prepare human PBL as stimulator cells
Date: 6 Oct 1998 05:32:31 -0700
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I'm seeking feedback as to whether x-ray irradiation, rather than gamma-irradiation, is used to prepare PBL stimulator cells for in vitro CTL cultures. Purchase of an x-ray generating unit, as opposed to an irradiator with a sealed gamma source, is less costly and engenders fewer regulatory and safety issues. 

I know of one company (Associated X-Ray Corp in East Haven, CT) which makes a suitable machine.  In fact, I used one of their units in years past when doing mouse T cell culture work.   However, I've never seen any investigator report in the literature that they prepared autologous stimulators for CD8+ T cell cultures by x-irradiation. Comments by anyone who does human T-cell culture work would be appreciated. 

Thanks. 

Geoffrey Cole 





From owner-immunology@net.bio.net Mon Oct 05 23:00:00 1998
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From: pjoseph@osucom-fs02.ocom.okstate.edu (Joseph A. Price, Ph.D.)
Newsgroups: bionet.immunology,sci.med.immunology
Subject: Re: Question about allergic reactions.
Date: 6 Oct 1998 17:07:30 GMT
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In article <AZLQ1.74$Mq1.187445@news.rdc1.on.wave.home.com>, sanyal@home.com 
says...
>
>I am very allergic to cats, ...
>
>When I returned to Canada, I was surprised that I did not display any
>allergic symptoms when I was exposed to cats. 

>However, it has now been 6 months since I returned and I have begun to
>redisplay the exact same symptoms again, 


It is most likely that your immune response to cat allergns waned without 
regular stimulation while you were abroad. Thus you were unreactive or 
subclinically reactive when you first returned. After enough reexposure and 
time, your immune responses to cat allergen were rekindled, and your problems 
returned.
 

Dept. Bioch. & Microbiol., OSU-COM
1111 W. 17th. St., Tulsa OK 74107
Ph. 918-561-8231  FAX 918-561-8414
pjoseph@osucom-fs02.ocom.okstate.edu
http://osu.com.okstate.edu/dept/basic/bio_micro/jprice.htm


From owner-immunology@net.bio.net Mon Oct 05 23:00:00 1998
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From: carlton@walleye.ccbr.umn.edu (Carlton Hogan)
Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
Subject: Re: "AIDS Treatment News" online * New Issue #302 (searchable/indexed)
Date: 6 Oct 1998 18:41:59 GMT
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In article <36193d76.113582531@netnews.worldnet.att.net>,
 <johnburgin@worldnet.att.net> wrote:
>On 5 Oct 1998 15:54:20 GMT, carlton@walleye.ccbr.umn.edu (Carlton
>Hogan) wrote:
>
>>
>>OK, let's take this thread back to it's beginning. I have answered your 
>>question. Now you explain why, if AZT is so toxic and non-beneficial,
>>is a survival benefit seen for AZT + *another* nuke + PI?
>>Put up or shut up.
>I don't have to do any such thing.  Remember, this is the internet,
>cyberspace, we, all of us, can have and express an opinion.  You were
>given a nice diatribe by Todd Miller, whom you readily dismissed as
>les incompetent.  Why should I expect any different treatment from
>you.  Not all are seeing the "survival benefit" from AZT +*another*
>nuke + PI.  That's still up for debate.  

Again, I would suggest that you demonstrate the specific flaws in
the dozen or so clinical trials that have shown an AIDS-free survival
benefit to combination therapy. Todd posted on a molecular biology 
concern, not a clinical one, having to do with phosphorylation
of AZT. What he probably didn't realize when he posted it is that 
arguing that little or no AZT gets phosphorylated pretty much
junks any statements about AZT being a terminater of host DNA.
If not enough gets phosphorylated to interfere with RT, then 
given the relative specificity of AZT, even less is available 
for interfering with host DNA synthesis.

Perhaps you should get a basic familiarity with the field: it would
save you from these embarassing revelations of your ignorance. If 
you like, I can refer you to some basic texts.

Carlton


From owner-immunology@net.bio.net Mon Oct 05 23:00:00 1998
Path: biosci!biosci!not-for-mail
From: Ilya Trakht <it8@columbia.edu>
Newsgroups: bionet.immunology
Subject: Staff Associate - Columbia University
Date: 6 Oct 1998 11:37:17 -0700
Organization: Columbia University
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Staff Associate position available to study the repertoire of human
antibodies to cancer-associated antigens and infectious agents. The
ongoing project is dealing with the development of totally human
monoclonal antibodies using hybridoma methodology and lymph tissues from
human subjects. The application of such antibodies in clinical medicine is
an ultimate goal of the project.

Position requires a degree in biological science and knowledge in this
field. Candidates with extensive experience in cell biology, molecular
biology, immunohistochemistry and immunology are encouraged to send their
curriculum vitae and three references to:

Ilya Trakht, Ph.D.
Department of Medicine, Columbia University
630 W 168 Street BB-1011
New York NY 10032

E-mail: it8@columbia.edu





From owner-immunology@net.bio.net Wed Oct 07 23:00:00 1998
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From: Phil Caskanette <caskanet@mc1adm.uwaterloo.ca>
Newsgroups: bionet.immunology,sci.med.immunology
Subject: Re: Question about allergic reactions.
Date: Tue, 06 Oct 1998 14:18:31 -0400
Organization: Univ. of Waterloo
Lines: 39
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Joseph A. Price, Ph.D. wrote:
> 
> In article <AZLQ1.74$Mq1.187445@news.rdc1.on.wave.home.com>, sanyal@home.com
> says...
> >
> >I am very allergic to cats, ...
> >
> >When I returned to Canada, I was surprised that I did not display any
> >allergic symptoms when I was exposed to cats.
> 
> >However, it has now been 6 months since I returned and I have begun to
> >redisplay the exact same symptoms again,
> 
> It is most likely that your immune response to cat allergns waned without
> regular stimulation while you were abroad. Thus you were unreactive or
> subclinically reactive when you first returned. After enough reexposure and
> time, your immune responses to cat allergen were rekindled, and your problems
> returned.

That sounds right based on my experience, and my allergists'
explanations.  I don't think a 'clean environment' has anything to do
with the phenomonen experienced by Steve.  My allergists said it was
dependent on whether you went somewhere that had sufficiently different
allergens from your normal environment.  I spent 2 years in Northern
Alberta and at first my allergies waned.  Then I developed allergies to
native plants in the region.  I thought it was a cold that wouldn't go
away, but it was allergies.  When I moved back to Ontario, my allergic
reactions waned and I felt fine for about 6 months.  Then the cycle
started again.  

-- 
======================================================================= 
Phil Caskanette                 |  e-mail: caskanet@UWaterloo.ca
Senior Auditor                  |  phone:  (519) 888-4567 x2774
University of Waterloo          |  fax:    
Waterloo, Ont., Canada N2L 3G1  |
======================================================================= 
Disclaimer: All expressed opinions are mine, and are not necessarily 
the views of my employer.

From owner-immunology@net.bio.net Wed Oct 07 23:00:00 1998
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From: govind_pgi@yahoo.com
Newsgroups: bionet.immunology
Subject: Re: PHA action mode help
Date: Wed, 07 Oct 1998 11:37:43 GMT
Organization: Deja News - The Leader in Internet Discussion
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In article <6velhs$pr2$1@nnrp1.dejanews.com>,
  strider@comteco.entelnet.bo wrote:
> Hello, can anybody tell me how the PHA works in the PBMC?
> I'm in Bolivia, and it's close to imposible for me to use
>  such tools as medline...
>
> Thanx 4 your help
>
> Cristina Alonso-Vega

 Hello there,

PHA is a lectin, means it binds to some sugar residues. Most probably it
binds some sugar residues attached to certain molecules on T cells and it
cross links those molecules. This transduces activation signals to T cells.
The important point is that presence of antigen presenting cells is
important.

This is as for as I know. Good luck

Govind
>
> ps please send me e-mail
>
> -----------== Posted via Deja News, The Discussion Network ==----------
> http://www.dejanews.com/       Search, Read, Discuss, or Start Your Own
>

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From owner-immunology@net.bio.net Wed Oct 07 23:00:00 1998
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From: johnburgin@worldnet.att.net
Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
Subject: Re: "AIDS Treatment News" online * New Issue #302 (searchable/indexed)
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On Wed, 07 Oct 1998 18:00:36 GMT, gmc0@ix.netcom.com (George M.
Carter) wrote:

>
>SNip...
>Me.>>
>>>They use 600.  Can't you read??  Well, asshole, this completely
>>>contradicts your lame assertion that people aren't dropping dead of
>>>"AZT induced AIDS" because the dosage is less.  It's not.
>
>The dentist:
>>And who says they're not dropping dead a little slower, which is my
>>contention?  Who can tell the difference between a slow death with AZT
>>and PI's and AIDS?  Why do you keep defending a bad drug?
>
>Well, that makes a lot of sense.  If "drugs cause AIDS" then lets add
>MORE toxic drugs to the mix and people will die more slowly.
If you're the first, sounds good to me.  jb
>
>Your logic is devastating.
>
>		George M. Carter
>
>


From owner-immunology@net.bio.net Wed Oct 07 23:00:00 1998
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From: strider@comteco.entelnet.bo
Newsgroups: bionet.immunology
Subject: PHA action mode help
Date: Wed, 07 Oct 1998 03:01:16 GMT
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Hello, can anybody tell me how the PHA works in the PBMC?
I'm in Bolivia, and it's close to imposible for me to use
 such tools as medline...

Thanx 4 your help

Cristina Alonso-Vega

ps please send me e-mail

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From owner-immunology@net.bio.net Wed Oct 07 23:00:00 1998
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From: astewar2@chat.carleton.ca (Andy Stewart)
Newsgroups: bionet.immunology
Subject: New Job Board / Skills Database for Hitech/Biotech
Date: 7 Oct 1998 18:18:29 GMT
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Check out Biotech Networks new biotech resource. The site offers free job
board access, resume posting and consolidated biotech resources. Check out
this invaluable resource at http://www.bionet.on.ca.




From owner-immunology@net.bio.net Wed Oct 07 23:00:00 1998
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From: andrew.devitt@nottingham.ac.uk (Chut)
Newsgroups: bionet.immunology
Subject: IL-14
Date: Thu, 08 Oct 1998 18:11:51 +0000
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Does anyone know of a supplier for IL-14.  Preferably in the UK or from a
company with a UK supplier.
Many thanks
Andrew

Please reply to:
andrew.devitt@nottingham.ac.uk

From owner-immunology@net.bio.net Wed Oct 07 23:00:00 1998
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From: "Scott Shanes" <sis@diedremoire.com>
Newsgroups: bionet.immunology
Subject: US-CA-RESEARCH ASSOCIATE MOLECULAR BIOLOGY
Date: Wed, 7 Oct 1998 17:28:16 -0000
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I am looking for a person to work in a lab that is identifying secreted
proteins used as therapeutic drug targets. You will utilize molecular
biology skills to perform Cloning, Plasmid and Phage Preparation, PCR,
making CDNA Libraries, Library Screening, Southern and Northern Blot
Analyses, Western Blotting, etc. Good communication and organizational
skills are a plus.
The candidate should possess a B.S., M.S. or MD degree. Our client is a
leading bio-tech company with research facilities in Central California and
can provide excellent benefits (health insurance, dental, and vision plan,
paid vacation and more). A high impact, high profile position with excellent
opportunity for advancement.
Please contact Scott Shanes by phone at 609-584-8733 Ext. 218, fax resume
and cover letter to 609-584-9575 or E-Mail to sis@diedremoire.com




From owner-immunology@net.bio.net Wed Oct 07 23:00:00 1998
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From: carlton@walleye.ccbr.umn.edu (Carlton Hogan)
Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
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In article <361c31dd.121102119@netnews.worldnet.att.net>,
 <johnburgin@worldnet.att.net> wrote:
>On Wed, 07 Oct 1998 18:00:36 GMT, gmc0@ix.netcom.com (George M.
>Carter) wrote:
>
>>
>>SNip...
>>Me.>>
>>>>They use 600.  Can't you read??  Well, asshole, this completely
>>>>contradicts your lame assertion that people aren't dropping dead of
>>>>"AZT induced AIDS" because the dosage is less.  It's not.
>>
>>The dentist:
>>>And who says they're not dropping dead a little slower, which is my
>>>contention?  Who can tell the difference between a slow death with AZT
>>>and PI's and AIDS?  Why do you keep defending a bad drug?
>>
>>Well, that makes a lot of sense.  If "drugs cause AIDS" then lets add
>>MORE toxic drugs to the mix and people will die more slowly.
>
If you're the first, sounds good to me.  jb

Does this mean that you have absolutely no intelligent response, and are 
unable to marshal any facts in this argument so you are resorting to 
personal attack? Brilliant strategy. Helps to confirm your stunning
critical insight, and command of the literature. Wanker.
(by the way, genius boy: you just said you would like George to
be the first to die more slowly - I am sure he is all choked up 
by your warm sentiment)

Carlton

From owner-immunology@net.bio.net Wed Oct 07 23:00:00 1998
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From: da_bruva@hotmail.com
Newsgroups: bionet.immunology
Subject: dentritic cells
Date: Thu, 08 Oct 1998 06:43:23 GMT
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Can anyone assist me with a clear protocol on purifing mouse dendritics
using 50% Percoll gradient....what exactly is 50% percoll gradients etc


much appreciated

Dave

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From owner-immunology@net.bio.net Wed Oct 07 23:00:00 1998
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From: gmc0@ix.netcom.com (George M. Carter)
Newsgroups: bionet.immunology,bionet.molbio.hiv,uk.people.health
Subject: Re: "AIDS Treatment News" online * New Issue #302 (searchable/indexed)
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SNip...
Me.>>
>>They use 600.  Can't you read??  Well, asshole, this completely
>>contradicts your lame assertion that people aren't dropping dead of
>>"AZT induced AIDS" because the dosage is less.  It's not.

The dentist:
>And who says they're not dropping dead a little slower, which is my
>contention?  Who can tell the difference between a slow death with AZT
>and PI's and AIDS?  Why do you keep defending a bad drug?

Well, that makes a lot of sense.  If "drugs cause AIDS" then lets add
MORE toxic drugs to the mix and people will die more slowly.

Your logic is devastating.

		George M. Carter



From owner-immunology@net.bio.net Wed Oct 07 23:00:00 1998
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From: robinb@leland.Stanford.EDU (Robin Blumenthal)
Newsgroups: bionet.immunology
Subject: Competitive PCR
Date: 8 Oct 1998 17:27:48 GMT
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Does anyone know of a company which sells kits  or products to do
competitive PCR- specifically I am looking for human interleukins
including IL-13

I would very much appreciate any information.

Thank you.

Robin Blumenthal
 -- 
 
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
Robin Blumenthal, Ph.D.                          
Department of Pediatrics, Rm S303
Stanford University 
300 Pasteur Drive
Stanford, California 94305

robinb@leland.stanford.edu                 
(650) 723-8224    (650) 498-4632 FAX
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

From owner-immunology@net.bio.net Wed Oct 07 23:00:00 1998
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From: govind_pgi@yahoo.com
Newsgroups: bionet.immunology
Subject: transfection
Date: Wed, 07 Oct 1998 13:09:40 GMT
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HEllo friends,

I am interested in ttransfecting adherent cells (liver cells) by calcium
phosphate mediated transfection. I want to know the protocol for transfecting
in 24 well or 6 well plates. The details like amount of DNA and volume of the
transfection solution are requested.

Thanks in advance

Govind

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From owner-immunology@net.bio.net Wed Oct 07 23:00:00 1998
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From: nigel.osborn@zetnet.co.uk (Nigel J.Osborn)
Newsgroups: bionet.immunology
Subject: Integration software for FPLC
Date: Wed, 07 Oct 1998 18:23:21 +0100
Organization: Amersham, Bucks
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Does anyone know of any integration software available for FPLC?

Ideally I would like to be able to scan in a chromatogram and get it to
tell me peak areas and relative peak areas.

Preferably shareware though commercial products also would probably be O.K.

Nigel Osborn.



From owner-immunology@net.bio.net Thu Oct 08 23:00:00 1998
Path: biosci!cica.es!alvarez
From: alvarez@cica.es (Jose Santos Alvarez)
Newsgroups: bionet.immunology
Subject: Flow cytometry of adhere