Re: Ethanol fixation

Micael Granstrom (mgranstrom@ume.foa.se)
Thu, 12 Sep 1996 07:16:10 +0200

Hi
I=B4m also new in this field but the method i have used for fixation is
ethanol fixation. The way I do it is as follows:
1. Centrifuge and wash cells twice with PBS
2. Pour off the PBS and resuspend the cells in the remaining drop.
3. Add 500 =B5l of Freeze-cold 95% ethanol.
4. Leave in a frezzer for 30 min.
5. Centrifuge down cells and wash twice with PBS

This is the way I do it and it works nice for me. If someone has a different
opinion about how to do it please don=B4t hesitate to correct me.

Micael Granstrom
FOA ABC-skydd
S-901 82 Umea
Sweden
e-mail mgranstrom@ume.foa.se

______________________________ Reply Separator=
_________________________________
Subject: Ethanol fixation
Author: "Bruce S. Hass" <BHASS@nctr.fda.gov> at Internet
Date: 9/10/96 10:50 PM

Hi,
I am interested in staining cells with Bodipy by the method of Gocze=20
and Freeman (Cytometry 17:151-158 1994), which calls for ethanol=20
fixed cells. Unfortunately the paper does not give details about the=20
fixation procedure. Is ethanol fixation so simple, obvious, or common?=20
Any suggestions on how to do it would be appreciated. Thanks.
=20
Bruce Hass
National Center for Toxicological Research=20
Jefferson AR 72079
(501) 543 7365
(501) 543 7745 (fax)
bhass@nctr.fda.gov=20


Home Page Table of Contents Sponsors Web Sites
CD ROM Vol 2 was produced by staff at the Purdue University Cytometry Laboratories and distributed free of charge as an educational service to the cytometry community. If you have any comments please direct them to Dr. J. Paul Robinson, Professor & Director, PUCL, Purdue University, West Lafayette, IN 47907. Phone:(317) 494-0757; FAX (317) 494-0517; Web http://www.cyto.purdue.edu EMAIL robinson@flowcyt.cyto.purdue.edu