From owner-dros@hgmp.mrc.ac.uk Mon Jul 29 15:07:11 2002 Return-Path: Received: from localhost (localhost [127.0.0.1]) by mercury.hgmp.mrc.ac.uk (Postfix) with SMTP id E458B17C56 for ; Mon, 29 Jul 2002 15:07:08 +0100 (BST) Received: from localhost (localhost [127.0.0.1]) by mercury.hgmp.mrc.ac.uk (Postfix) with ESMTP id 15C8D17B65 for ; Mon, 29 Jul 2002 15:07:05 +0100 (BST) Received: by mercury.hgmp.mrc.ac.uk (Postfix, from userid 6020) id B6C5B17C44; Mon, 29 Jul 2002 15:06:57 +0100 (BST) Received: from localhost (localhost [127.0.0.1]) by mercury.hgmp.mrc.ac.uk (Postfix) with ESMTP id 8840A17AE7 for ; Thu, 25 Jul 2002 16:32:40 +0100 (BST) Received: by mercury.hgmp.mrc.ac.uk (Postfix, from userid 60001) id E2E1C17ABB; Thu, 25 Jul 2002 16:32:36 +0100 (BST) To: bionet-drosophila@net.bio.net From: andreao@skio.peachnet.edu (Andrea Osterlehner) Newsgroups: bionet.drosophila Subject: Genomic DNA extraction Organization: BIOSCI/MRC Human Genome Mapping Project Resource Centre Message-ID: <3D4019FC.AFBFE2E@skio.peachnet.edu> MIME-Version: 1.0 Content-Type: text/plain; charset=us-ascii Content-Transfer-Encoding: 7bit X-Received: from localhost (localhost [127.0.0.1]) by mercury.hgmp.mrc.ac.uk (Postfix) with ESMTP id 97F4917AFD for ; Thu, 25 Jul 2002 16:32:33 +0100 (BST) X-Received: from ahab.skio.peachnet.edu (ahab.skio.Peachnet.EDU [168.20.254.11]) by mercury.hgmp.mrc.ac.uk (Postfix) with ESMTP id 5AD1917ABB for ; Thu, 25 Jul 2002 16:32:29 +0100 (BST) X-Received: from skio.peachnet.edu (pip [168.20.254.1]) by ahab.skio.peachnet.edu (8.11.6+Sun/8.11.3) with ESMTP id g6PFX2S20119 for ; Thu, 25 Jul 2002 11:33:07 -0400 (EDT) X-Mailer: Mozilla 4.79 [en] (Windows NT 5.0; U) X-Accept-Language: en X-To: dros@net.bio.net Date: Mon, 29 Jul 2002 15:06:57 +0100 (BST) X-Razor-id: 31adf1a85e1378e07f132113d36d922598d5037e Sender: owner-dros@hgmp.mrc.ac.uk Precedence: bulk Hallo, I am struggling with the isolation of genomic DNA of Drosophila. First I tried a tissue kit which worked well for marine organisms but did not work for Drosophila. Next I tried a protocol using frozen flies, grinding them in a buffer containing SDS, Sucrose and EDTA, heating, Phenol-Chloroform extraction and final EtOH precipitation. The DNA yield was poor too, only 140 ng from 15 flies. For a southern blot experiment I need much more genomic DNA. I would be glad if somebody could send me a protocol, which works well. Thanks a lot, Andrea. --- .