Hi Liz,
Get it. Thank you for the detailed procedures.
Best Regards,
Victor
From: Elizabeth Chlipala
To: Victor Wong ; Tony Henwood (SCHN)
; "histonet@lists.utsouthwestern.edu"
Sent: Wednesday, February 20, 2013 12:15 AM
Subject: RE: [Histonet] Safranin O staining
Victor
processing.
BTW, I don't have access right to the paper. Anyway, the staining pictures on
the website are very nice.
Once, thank you for your help.
Best Regards,
Victor
From: Elizabeth Chlipala
To: Victor Wong ; Tony Henwood (SCHN)
; "histonet@lists.utsouthwestern.edu"
r
sources.
P.S. unforuntuately we don't have a Haematology department but may be we can
try other cells.
Best Regards,
Victor
From: Tony Henwood (SCHN)
To: 'Victor Wong' ; "histonet@lists.utsouthwestern.edu"
Sent: Tuesday, February 19, 2013 6:44 AM
Subject: RE:
arose may be
deletrious to the staining. As suggested, I will extend the fixation time.
Best Regards,
Victor
From: "koelli...@comcast.net"
To: Victor Wong
Cc: histonet@lists.utsouthwestern.edu
Sent: Monday, February 18, 2013 10:42 PM
Subject: Re: [Histonet] Safranin O stain
imes, or follow a known protocol (you can find that in
either Peter Gray's or Lillie's books).
René J.
From: Victor Wong
To: "histonet@lists.utsouthwestern.edu"
Sent: Sunday, February 17, 2013 9:34 PM
Subject: [Histonet] Safranin O staining
Hi all,
I am working on ind
by chondrogenic pellet can be destroyed by heat?
Best Regards,
Victor
From: Tony Henwood (SCHN)
To: 'Victor Wong' ; "histonet@lists.utsouthwestern.edu"
Sent: Monday, February 18, 2013 11:45 AM
Subject: RE: [Histonet] Safranin O staining
Victor,
Heat can affect the way ti
your processing
protocol?
Best Regards,
Victor
From: Tony Reilly
To: "histonet@lists.utsouthwestern.edu" ;
Victor Wong
Sent: Monday, February 18, 2013 1:50 PM
Subject: Re: [Histonet] Safranin O staining
Hi Victor
I have been using agar cell blocks for over 30 years. It h
Hi all,
I am working on induced chondrogenesis in cell culture. After, induction, I
put the clump of cells (pellets) in 2% agarose to make a cell block. When the
pellet did not sink to the bottom of agarose, I heated to melt the agarose
again and centrifuged with higher speed. I fix the agar
Dear all,
Thank you for all the professional suggestion of the previous IHC staining and
finally I got some positive results.
Then comes problem on the PECAM-1 IHC. I am using the Santa Cruz sc-1506R (it
is a anti-RAT antibody from RABBIT). I stain decalcified rat spine paraffin
sections,
Dear all,
I am working on imumunohistichemistry of ki-67 antibody (DAKO MIB-5, a
monoclonal mouse anti-rat) on EDTA-decalcifed rat spine and femur. I used
DAKO's reagents such as Dual enzyme block, antigen retrieval solution pH6.0,
normal goat serum, anti-mouse Envision plus kit and the DAB k
Dear all,
I am going to decal and process PIG femur and lumbar vertebrates. I only have
experience on soft tissues. Anyone can suggest any protocols in
decalcification and processing? Many thanks in advance.
Cheers,
Victor
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