Dear Neeraj,
The fixation, not membrane permeabilization, seems to be more of
a factor for nuclear proteins.
Try Methanol (100% formaldehyde-free at -20C for 20 min). Compare
with 3.7% FA at RT.
Contact me off-list if you need further details.
Besrt Wishes,
Fred E. Indig, Ph.D.
Head, Confocal Imaging
Facility
Hi List, One of my colleagues is trying to visualize a nuclear protein using primary antibodies. Is there a special trick or protocol that allows the primary and the fluorescent secondary antibodies better access to proteins inside the nucleus? They have already considered using either Triton or Tween-20. Thanks, Neeraj. Neeraj V. Gohad, Ph.D. Postdoctoral Fellow Okeanos Research Group Department of Biological Sciences 132 Long Hall Clemson University Clemson,SC-29634 Phone: 864-656-3597 Fax: 864-656-0435 Please note my new email address: [hidden email] -- |
Dear Fred, Thanks for the reply, I forwarded your suggestion to my colleague,
and would much appreciate any further suggestions. Best, Neeraj. Neeraj V.
Gohad, Ph.D. Postdoctoral
Fellow Okeanos
Research Group Department of
Biological Sciences 132 Long Hall Clemson
University Clemson,SC-29634 Phone:
864-656-3597 Fax:
864-656-0435 Please note
my new email address: [hidden email] From: Confocal Microscopy
List [mailto:[hidden email]] On Behalf Of Fred E.
Indig, Ph.D. Dear Neeraj, The fixation, not membrane permeabilization, seems to be
more of a factor for nuclear proteins. Try Methanol (100% formaldehyde-free at -20C for 20 min).
Compare with 3.7% FA at RT. Contact me off-list if you need further details. Besrt Wishes, Fred E. Indig, Ph.D. Head, Confocal Imaging Facility
-- |
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