Re: IHC Question
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From: | rschoonh@sph.unc.edu |
To: | Patsy.Ruegg@UCHSC.edu, histonet@Pathology.swmed.edu |
Reply-To: | |
Date: | Thu, 11 Mar 1999 08:30:55 -0500 (Eastern Standard Time) |
Content-Type: | TEXT/PLAIN; CHARSET=US-ASCII |
Patsy,
I routinely add Tween 20 to my wash buffer but not BSA. I do use 1% BSA in my
antibody dilution buffers but not Tween 20. I have also noticed that
concentrations of Tween 20 noted in the literature varies from 0.05% to 1.0%, I
have always used 1.0% with no problems but I'm interseted in what others are
using and why.
-- Begin original message --
>
> I have been having trouble with non-specific background staining and have
> gone to putting acetylated BSA in my wash buffer, which helps. My question
> is: is there any reason not to also put the TWEEN in the wash buffer, it
> seems that I read something a while back suggesting that they should not be
> used together??????
> Patsy Ruegg
>
>
-- End original message --
best regards,
Bob
Robert Schoonhoven
Laboratory of Molecular Carcinogenesis and Mutagenesis
Dept. of Environmental Sciences and Engineering
University of North Carolina
CB#7400
Chapel Hill, NC 27599
Phone
office 919-966-6343
Lab 919-966-6140
Fax 919-966-6123
**Suppose you were an idiot... And suppose you were a member of Congress ...
But I repeat myself.-Mark Twain**
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