Re: Methods of Image Analysis

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From:rschoonh@sph.unc.edu
To:cboccia@mail.med.cornell.edu ("Claire G. Boccia"), Histonet@Pathology.swmed.edu
Reply-To:
Date:Thu, 27 May 1999 10:47:48 -0400 (Eastern Daylight Time)
Content-Type:TEXT/PLAIN; CHARSET=US-ASCII

I have been using the BioQuant system by R&M Biometrics for years and I love
it!  It is a true color system so it really does't matter what your chromagen
is.  I'm using the Windows 98 version (upgraded a few months ago).  I use it
for cell proliferation studies, area analysis, density and bone morphology.  It
has even more functions that I do not use at this time (but ya never know). It
is an open system in that the user can configure the system his/her own needs. 
Please note that I have NO affiliation with this company, I just LOVE their
system.   

Their number is 800-221-0549.  They also have a web site but I lost my bookmark
file so I don't have it handy at this time.

-- Begin original message --
> 
> Dear Histonetters,
> 
> I am intested in performing image analysis using a better system than the 
> one I use now, which is an old CAS 200.  My chromagen is DAB and my 
> counterstain is methyl green, the two stains the CAS 200 systems best 
> detects.  Are fluorescent analysis systems better?  Could I do surface 
> area measurements with a more advanced system?  I would like to quantify 
> staining with  less variability than I get now.  My standard deviations per
> experiment are very high.
> 
> Thanks in advance for your advice!
> 
> Claire Boccia
> Weill Medical College
> New York, New York 

-- 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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