Could anybody help me please: what is the usual concentration range for
Saponin as a detergent in immunocytochemistry, on 10-30 um cryostat
sections?
(I'm trying to improve AB penetration, Triton doesn't seem to do the job;
I would therefore start at the stronger end of the Saponin concentration
spectrum.)
Also, do you recommend the stuff in all buffers (AB dilution, wash) or
just as a pretreatment before AB incubation, with Triton in all following
steps?
Your help would be very much appreciated.
Swidbert
--
Swidbert R. OTT
Dept. Zoology, Univ. Cambridge/UK
