Hi there,
Does anybody know of a good alternative to nail polish for sealing round
coverslips (or any shape, for that matter!).
Ideally I am looking for a solution that is both an aqueous mount media and
sealant, if such a beast exists...
Thanks!
Gil
PS: Happy New Year!
--
Guillermo Palchik
a good working protocol that could share with me? It would be
greatly appreciated...
Thanks
Gil
--
Guillermo Palchik
Ph.D. Candidate - Interdisciplinary Program in Neuroscience
Georgetown University Medical Center
Research Building Room W 217
3970 Reservoir Rd. NW, Washington, DC 20007
Lab: 202-687
, could I do overnight incubations?
the tissue is flash frozen, but it does get fixed at the beginning of the
protocol with PFA (4%) and subsequently with acetic acid-EtOH.
Thanks,
Gil
--
Guillermo Palchik
Ph.D. Candidate - Interdisciplinary Program in Neuroscience
Georgetown University Medical
Dear Histoneters,
I am looking for help regarding flash freezing of rat pup brains
(Postnatal day 8). We need the tissue to be fresh (unfixed) for
cutting at the cryostat.
So far the technique has been:
1- to scoop the brains straight into cold (-50 C) Isopentane for
about 10 seconds,
about the sucrose? does it remove the
water?
I'd appreciate your thoughts...
Best,
Guillermo
Guillermo Palchik
g...@georgetown.edu
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Hi there,
I am having problems with my brain sections (15 um - flash-frozen)
curling up once I remove the antiroll plate on my cryostat... does
anyone know how i can prevent this?
Also - does anybody have a quick guide on what to improve while
cutting, based on the damage seen on the
Dear Histologists,
Does anyone have a good protocol for doing TUNEL on fixed brain slides?
Thanks
Guillermo Palchik
g...@georgetown.edu
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as a perfusate and see if this would allow us to do the TUNEL.
I would appreciate any comments and suggestions regarding this. I am
sorry for the lengthy email, but I wanted to show a more or less
complete picture, in case I am overlooking other factors…
Guillermo Palchik
g...@georgetown.edu