Re: [Histonet] orienting mouse embryos
Try putting a few mls of aqueous eosin in your fixative. A pink specimen is
a lot easier to see.
The eosin can be washed out at a later stage if it is not required.
Good luck and regards, Laurie.
At 04:53 PM 10/05/04 -0500, email@example.com wrote:
>Could I tap your collective experience to help solve a problem? I am trying
>to orient gestational day 9.5 mouse embryos in paraffin for cross
>sectioning. After processing, these specimens are like pieces of fragil
>white pepper. I can only see head from tail with a microscope. By the time
>I get everything in focus the parffin is turning white....like finding a
>ghost in a blizzard. Does anyone have any tips for this task? Thanks, Lin
>Department of Genetics, Cell Biology, and Anatomy
>University of Nebraska Medical Center
>Omaha, NE 68198-5455
>Histonet mailing list
Mr.Laurie Reilly Ph 07 4781 4468
Physiology & Pharmacology Fax 07 4779 1526
Aust.Inst.of Tropical Vet.& Animal Sc.
James Cook University
Histonet mailing list
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