From owner-drosophila@net.bio.net Sun Nov 27 22:00:00 1994 Path: biosci!bloom-beacon.mit.edu!uhog.mit.edu!europa.eng.gtefsd.com!howland.reston.ans.net!pipex!uknet!daresbury!not-for-mail From: oujac@vax.ox.ac.uk Newsgroups: bionet.drosophila Subject: Re mapping Df's by PCR Date: 28 Nov 1994 12:34:39 -0000 Lines: 11 Sender: lpddist@mserv1.dl.ac.uk Distribution: bionet Message-ID: <3bciov$7tr@mserv1.dl.ac.uk> Original-Sender: oujac@uk.ac.ox.vax Original-To: DROS@dl.ac.uk Hi Dr. Shaffer and all interested, There is a way of mapping Df(3)'s that I know of using a similar technique. What one does in fact is to have an embryonic phenotype for recognising the embryos that do _not_ carry the Df - not as direct as positive selection, but perhaps the best option currently available. We have a TM3 balancer marked with beta-gal under the hb promoter (expressed in the early embryo, among other times). If the Df(3) survives over TM3, make a stock of Df(3)/TM3 hb-beta-gal, collect eggs, stain blue and PCR white eggs. Is this any help? Of course it's limited to Df(3)'s that are fertile over TM3. Ben Yudkin .