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	<title>Comments on: Profile my DNA, babe.</title>
	<link>http://www.metafilter.com/29600/Profile-my-DNA-babe/</link>
	<description>Comments on MetaFilter post Profile my DNA, babe.</description>
	<pubDate>Sat, 15 Nov 2003 09:37:21 -0800</pubDate>
	<lastBuildDate>Sat, 15 Nov 2003 09:37:21 -0800</lastBuildDate>
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		<title>Profile my DNA, babe.</title>
		<link>http://www.metafilter.com/29600/Profile-my-DNA-babe</link>	
		<description>DNA profiling may be a &lt;a href=&quot;http://www.pbs.org/wgbh/pages/frontline/shows/case/revolution/&quot;&gt;complex issue&lt;/a&gt;,  but whatever your take, go ahead and try your hand at genetic sleuthing with &lt;a href=&quot;http://www.biotechnology.gov.au/biotechnologyOnline/interactives/dna_profile_interactive.htm&quot;&gt;this&lt;/a&gt; spiffy flash interactive.</description>
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		<pubDate>Sat, 15 Nov 2003 08:10:21 -0800</pubDate>
		<dc:creator>moonbird</dc:creator>		<category>dna</category>		<category>genetic</category>		<category>flash</category>		<category>brokenlink</category>
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		<title>By: majick</title>
		<link>http://www.metafilter.com/29600/Profile-my-DNA-babe#585295</link>	
		<description>It&apos;s not terribly interactive, consisting chiefly of &quot;click here, click there, yay, you did it!&quot;  Nevertheless it&apos;s a good, bite-sized explanation of the DNA profile matching process.</description>
		<guid isPermaLink="false">comment:www.metafilter.com,2003:site.29600-585295</guid>
		<pubDate>Sat, 15 Nov 2003 09:37:21 -0800</pubDate>
		<dc:creator>majick</dc:creator>
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		<title>By: Belgand</title>
		<link>http://www.metafilter.com/29600/Profile-my-DNA-babe#586639</link>	
		<description>Eh, pretty good for the layman, but I do research in a molecular genetics lab and thus do this sort of thing every day.

Want a more realistic idea of what gel electrophoresis is like? Well, first you make up a tube consisting of a very small (like 20 microliters or 20*10^-6 or 20 millioneths of a liter) amount of DNA to run and a bit of loading buffer. Basically it&apos;s a blue dye that you can see on the gel as it runs and use to detect bands later on. Then we make up the gel itself. It&apos;s a lot like making Jell-O really. Add some powder to some liquid, boil, pour into the mold, put a &quot;comb&quot; into it, and let it cool down. The comb is a bit of plastic with some little nubs sticking down and will create wells in the gel. You then place the gel in it&apos;s tray into a gel box, add some fluid, and then load the DNA/buffer solution into the wells (you use a micropipeter, not an eyedropper, but it&apos;s kinda, sorta the same idea). Plug the box into a power supply and wait about 3 hours or so.  Pull the tray out and place the gel in a tray containing some water, add some ethidiome bromide (careful, it&apos;s mutagenic!) to this and let it stain for 15 min. or so. Then look at it under a UV lamp and you&apos;ll see banding.

If you want a scale you need to also run a marker, a bit of DNA that has already been digested with the size of each band already known. Each gel will look different so you need to use a marker every time as it won&apos;t look the same twice. Also interpreting the bands can be a bit tough. Very rarely are they ever as clear and discrete as shown for a variety of reasons.

It&apos;s honestly a very simple procedure and something almost anyone could be taught to do in about 20-30 min.</description>
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		<pubDate>Tue, 18 Nov 2003 00:03:56 -0800</pubDate>
		<dc:creator>Belgand</dc:creator>
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