Desok Kim dkim at
Mon Feb 5 14:42:53 EST 1996

Dear colleagues,
I have some problem in my frozen sections. I prepared a slide by just putting 
some mounting media(triglycerol) and a coverslip on the dried tissue section.
Under the rhodamine filter set, the cells are all autofluoresing very bright. 
Under other filter sets(FITC, DAPI), they are a little less bright but still 
significant. They were cut from a piece of frozen normal (BPH) prostate 
tissue. Any substances in prostate tissue cause this or possible contamination 
during the tissue preparation?

Desok Kim, PhD                           Phone:919-966-2574
Post Doctoral Research Associate         Fax  :919-966-5722
Urology/Surgery                          email:dkim at
UNC School of Medicine
Chapel Hill, NC 27599-7235, USA

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