Re: sucrose/OCT
<< Previous Message | Next Message >>
From: | Mary Latimer <ml4@st-andrews.ac.uk> (by way of histonet) |
To: | histonet@histosearch.com |
Reply-To: | |
Content-Type: | text/plain; charset="us-ascii" |
If it is any benefit I agree with this message.... my tissue is rat brain
I have used glycerin in the past but found no benefit...Mary
On Fri, 29 Oct 1999, Geoff McAuliffe wrote:
> denise M m Long-Woodward wrote:
>
> > Hi! I'm looking for instructions on how to "cryopreserve" mouse tissue
> > using sucrose and OCT. Details will be appreciated. Many thanks for your
> > insight.
>
> Denise:
>
> After fixation and several buffer washes, I soak the tissue in cold 10%
> sucrose in buffer until it sinks,usually 1-3 hours depending on size. Then
> cold 20% sucrose in buffer until it sinks which is usually overnight. I have
> used concentrations of sucrose as high as 30% but see no benefit. I only use
> OCT to "glue" the tissue to the microtome stage.
> Rapid freezing of the tissue is very important to prevent ice crystal
> artifacts!
>
> Good luck,
> Geoff
> --
> **********************************************
> Geoff McAuliffe, Ph.D.
> Neuroscience and Cell Biology
> Robert Wood Johnson Medical School
> 675 Hoes Lane, Piscataway, NJ 08854
> voice: (732)-235-4583; fax: -4029
> mcauliff@umdnj.edu
> **********************************************
>
>
>
>
<< Previous Message | Next Message >>