{"id":415,"date":"2012-01-26T09:44:31","date_gmt":"2012-01-26T13:44:31","guid":{"rendered":"http:\/\/www.ttgnet.com\/journal\/?p=415"},"modified":"2012-01-26T09:44:31","modified_gmt":"2012-01-26T13:44:31","slug":"thursday-26-january-2012","status":"publish","type":"post","link":"https:\/\/www.ttgnet.com\/journal\/2012\/01\/26\/thursday-26-january-2012\/","title":{"rendered":"Thursday, 26 January 2012"},"content":{"rendered":"<p><span style=\"font-weight: bold; color: #000099; font-family: Arial;\">08:44 &#8211;<\/span><span style=\"font-family: Arial;\"> I sent off the preface and lab safety chapter to the reviewers yesterday. That leaves the introduction, which is well in progress, and a lab session that I wasn&#8217;t sure I&#8217;d have time to do before deadline. That one is on simulated DNA gel electrophoresis, &#8220;simulated&#8221; because we&#8217;ll use dyes rather than actual DNA fragments for the separation.<br \/>\n<\/span><\/p>\n<p><span style=\"font-family: Arial;\">Those dyes&#8211;crystal violet, methylene blue, and safranin O&#8211;are included in the kit as biostains, and they all migrate the same direction in a gel. We&#8217;ll use their different molecular masses as proxies for DNA fragments of differing BP size. We&#8217;d use real DNA, but that&#8217;d require expensive restriction enzymes, and wouldn&#8217;t produce very distinct banding in an agar gel (as  opposed to agarose, which is much, much more expensive than agar, which isn&#8217;t cheap itself). I was thinking about having readers pre-run the gels to clear out some of the gunk that&#8217;s present in plain agar, but that&#8217;s really more trouble than it&#8217;s worth.<br \/>\n<\/span><\/p>\n<hr style=\"width: 65%; height: 3px; font-family: Arial;\" \/>\n","protected":false},"excerpt":{"rendered":"<p>08:44 &#8211; I sent off the preface and lab safety chapter to the reviewers yesterday. That leaves the introduction, which is well in progress, and a lab session that I wasn&#8217;t sure I&#8217;d have time to do before deadline. That one is on simulated DNA gel electrophoresis, &#8220;simulated&#8221; because we&#8217;ll use dyes rather than actual DNA fragments for the separation.\n<\/p>\n<p>Those dyes&#8211;crystal violet, methylene blue, and safranin O&#8211;are included in the kit as biostains,<\/p>\n<p> <a href=\"https:\/\/www.ttgnet.com\/journal\/2012\/01\/26\/thursday-26-january-2012\/\">&nbsp;&raquo;&nbsp;Read more about: Thursday, 26 January 2012 &nbsp;&raquo;<\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"footnotes":""},"categories":[40],"tags":[],"class_list":["post-415","post","type-post","status-publish","format-standard","hentry","category-writing"],"_links":{"self":[{"href":"https:\/\/www.ttgnet.com\/journal\/wp-json\/wp\/v2\/posts\/415","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.ttgnet.com\/journal\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.ttgnet.com\/journal\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.ttgnet.com\/journal\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.ttgnet.com\/journal\/wp-json\/wp\/v2\/comments?post=415"}],"version-history":[{"count":0,"href":"https:\/\/www.ttgnet.com\/journal\/wp-json\/wp\/v2\/posts\/415\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.ttgnet.com\/journal\/wp-json\/wp\/v2\/media?parent=415"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.ttgnet.com\/journal\/wp-json\/wp\/v2\/categories?post=415"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.ttgnet.com\/journal\/wp-json\/wp\/v2\/tags?post=415"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}