Team:NGSS TR/isolation.html
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+ | <h1>PROTOCOLS</h1> | ||
+ | <blockquote> | ||
+ | <h2><span class="gfdg">4.ISOLATION</span></h2> | ||
+ | <blockquote> | ||
+ | <p>1-Liquid cultures centrifuge at 13000 rpm 10 minuites.<br /> | ||
+ | 2- After the centrifuge decant the supernatant and remove all medium residue by pipet.<br /> | ||
+ | 3-Completely resuspend the cell pellet in 250 ul of resuspension solution by voretxing. <br /> | ||
+ | 4-Add 250 ul lysis solution and invert 4-6 times to lyse the cells. Incubate at room temperature for 3 minutes.<br /> | ||
+ | 5-Add 350 ul neutralization solution and invert 4-6 times.<br /> | ||
+ | 6- Centrifuge at 13000 rpm, 5 minutes.<br /> | ||
+ | 7- Transfer the supernatant carrefully to the coloumn. <br /> | ||
+ | 8- Centrifuge at 13000 rpm, 1 minute. Discard the flow through. <br /> | ||
+ | 9- Wash the coloumn once with 500 ul wash solution by centrifuging for 60 seconds at 13000 rpm and discard the flow through.<br /> | ||
+ | 10- Repeat the wash procedure (step 9)<br /> | ||
+ | 11-Transfer the coloumn into a fresh 1.5 ml centrifuge tube <br /> | ||
+ | 12- Add 50 ul elution buffer <br /> | ||
+ | 13- Incubate for 2 min at room temperature and centrifuge for 2 min (13000 rpm) </p> | ||
+ | </blockquote> | ||
+ | </blockquote> | ||
+ | <p> | ||
+ | <blockquote> | ||
+ | </p> | ||
+ | </blockquote> |
Revision as of 11:33, 20 June 2014
PROTOCOLS
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