From owner-cellbiol@net.bio.net Sun Feb 02 22:00:00 1997 Newsgroups: bionet.cellbiol Path: biosci!bloom-beacon.mit.edu!spool.mu.edu!howland.erols.net!surfnet.nl!news.belnet.be!news.vub.ac.be!hnets.uia.ac.be!news From: overveld@uia.ua.ac.be (Labo Longziekten) Subject: Re: Percolls-cell clumping X-Nntp-Posting-Host: pcgent22.uia.ac.be Message-ID: Followup-To: Colin.Farquharson@bbsrc.ac.uk Sender: news@uia.ua.ac.be (News database) Organization: Univ. Antwerp (U.I.A.) X-Newsreader: Date: Mon, 3 Feb 1997 13:01:04 GMT Lines: 18 In article <32EE2006.4C07@bbsrc.ac.uk>, Colin Farquharson writes: >I am trying to separate chondrocytes into their different sizes using >Percoll (Pharmacia) discontinuous gradients (1.04 - 1.08). Things often works but often there is >extensive clumping at the 1.06 band and this results in poor >separation. Did you ever try to add some DNAse to your cell suspension before you separate them? We do when we isolate cells from the lung. We used concentrations of 0.01-0.05 mg/ml. I hope this will help. Frans J. van Overveld, PhD Dept. Resp. Med. Univ. Antwerp, Belgium .