very mouse biology small lab, I do all the
processing, cutting, and staining myself. So, what works for me may
not be feasible for everyone, and may still not be the best way to do
things (although I do try to generate beautiful data).
Sincerely,
Nicole Collette
LLNL/ UC Berkeley
At
Hi, Emily,
We use Salmon Testes DNA for our hyb buffer for whole mount RNA in
situ on mouse and frog embryos, Sigma catalog # D-9156, comes in 5 x
1ml (11.0 mg/ml) tubes. It says "for hybridization" on the package
;) Hope that helps.
Sincerely,
Nicole Collette
Lawrence Livermor
k the contamination. However, I'm not in a
high-throughput lab, so this works for me (I'm a one-pair-of-hands
histology lab).
Sincerely,
Nicole Collette
Lawrence Livermore National Lab/ UC Berkeley
At 11:59 AM -0500 2/24/10, Amos Brooks wrote:
Hi,
I have been making up my own
treatment (and more washing) cannot or should not be used? I
tried them together on my unstained slides, they look pretty darn
fabulous. Just striving for clean data and beautiful pictures.
Thanks again for all your help,
Sincerely,
Nicole Collette
Lawrence Livermore Natio
ging and labeling though...), but don't want to
just send a giant box and have them all broken on the other end.
Maybe there's another alternative? I'm sure someone on histonet has
done this before :)
Thanks in advance for the advice.
Sincerely,
Nicole Collette
Lawrence Livermore Na
Temperature is also somewhat of a factor, I've
found that I would section at colder temperature than I normally
would for that tissue to get it to crosslink well- sounds
counterintuitive, but there it is. This is purely based on my own
trial and error, take it with a grain of salt and good
ork like Fast Garnet GBC, as a red
stain?), and assorted acids and buffers if that makes a difference. I
am happy to purchase additional reagents that will work. Thanks so
much for your help and support!
Sincerely,
Nicole Collette
Lawrence Livermore National Lab
ieval is the same? Thanks for the advice!
Sincerely,
Nicole Collette
LLNL/UCB
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7;s a lot of good info here, and some
really great expertise, but finding it threaded through the archives
is not the easiest way to find this stuff, and it is evident by the
discussions that come up over and over. Thanks for listening! Keep up
the good work!
Sincerely,
Nicole Collette
_ At
vice
from this listserv.
Sincerely,
Nicole Collette
LLNL/UCB
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fantastic sections. I suspect it could be incomplete washing of the
EDTA before infiltration, but it's possible that the processing
schedule is just not long enough. Any advice?
Thanks in advance! Happy Friday!
Sincerely,
Nicole Collette
Lawrence Livermore National L
Nicole Collette
LLNL
postdoc
Good point. I never tested it directly side-by-side to check for the
effects of 1% methanol directly. It could be old-fashioned paranoia.
However, it was a variable I wanted to omit as I know methanol (we
are talking 100%) has deleterious effects to some mouse antigens
this protocol
with (or without) success, I'd be grateful for
the advice.
Thanks in advance,
Nicole Collette
LLNL/UCB
[EMAIL PROTECTED]
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