Posted by
Armen Khatchadourian on
URL: http://confocal-microscopy-list.275.s1.nabble.com/autofluorescence-in-liver-tissue-tp7580412p7580419.html
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I had a similar problem with paraffin-embedded pancreatic sections. But I was getting much less autofluorescence in the far red region, compared to green and red, hence I started using AlexaFluor 647 -labeled secondary antibodies. I don't know if this would work for liver though.
Best,
Armen
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Sent: Tuesday, June 04, 2013 5:23 PM
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Subject: Re: autofluorescence in liver tissue
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Autofluorescence can be especially bad for paraffin-embedded sections. I'm not sure liver is particularly worse, though, compared to many tissues.
I've had very good luck with sodium borohydride washing to reduce autofluorescence, particularly in the green and red range.
Another thing I've found to reduce it is to use Histoclear or other limonine solvents for deparaffinization, instead of xylenes.
Another thing to try is to amplify your label, to help overcome the background, using biotin/streptavidin, Tyramide signal amplification, or Qdots.
Hope that helps. Cheers,
Jason
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Sent: Tuesday, June 04, 2013 10:24 AM
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Subject: autofluorescence in liver tissue
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I am working with a lab looking at IF stained sections of formalin-fixed, paraffin embedded pieces of mouse or rat liver. If there was any actual staining in their first try on our confocal, it was largely washed out by the lovely and strong autofluorescence. Because their animal experiment takes 8 weeks, it's not trivial (or inexpensive) to get new tissue, so they have been using existing blocks. No one in their lab had the foresight to put up snap-frozen tissues for cryosectioning. I have them looking at this document:
http://www.uhnres.utoronto.ca/facilities/wcif/PDF/Autofluorescence.pdf but I'm wondering if liver is always a problem with autofluorescence, or is there maybe something in this lab's sample prep protocol that's making it worse. Any ideas?
Doug
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