From owner-celegans@net.bio.net Thu Nov 03 22:00:00 1994 Path: biosci!rutgers!uwm.edu!cs.utexas.edu!howland.reston.ans.net!usc!elroy.jpl.nasa.gov!netline-fddi.jpl.nasa.gov!nntp-server.caltech.edu!news From: kayne@caltech.edu (paul kayne) Newsgroups: bionet.celegans Subject: Re: killing adults Date: 4 Nov 1994 20:32:41 GMT Organization: cal tech Lines: 25 Sender: -Not-Authenticated-[3545] Distribution: world Message-ID: <39e5p9$l5t@gap.cco.caltech.edu> References: <1C999B65380@charon.biochem.wisc.edu> NNTP-Posting-Host: ginger.bio.caltech.edu X-Posted-From: InterNews 1.0.2@ginger.bio.caltech.edu Xdisclaimer: No attempt was made to authenticate the sender's name. In article <1C999B65380@charon.biochem.wisc.edu> FERGUSON@BIOCHEM.WISC.EDU writes: > I am wondering if there is any chemical or physical procedure I could > use to kill adult worms without killing embryos. I am trying to isolate > a large quantity (from liquid) of homozygous deficiency embryos. I > would like to avoid bleach treatment if possible since even short bleach > treatments will kill a fraction of the embryos and contaminate my prep. > > Thanks- > Kim Ferguson i have succesfully used nytex filters to obtain specific stages. the exact condition depend on the particular strain, but embryos will go through a 15 um filter and adults won't. it would be helpful to do this with synchronized cultures, as it is sometimes difficult to separate adjacent stages. also a preselection can be useful, that is a 1 X g spin - putting all the worms in M9 in an orange cap tube and letting them sit for 2-10 minutes. adults will sink much faster than other stages. paul kayne kayne@caltech.edu .