Team:NGSS TR/isolation.html
From 2014hs.igem.org
(Created page with "<html xmlns="http://www.w3.org/1999/xhtml"> <head> <meta name="keywords" content="" /> <meta name="description" content="" /> <script type="text/javascript" src="jquery-1.7.1.min...") |
|||
(2 intermediate revisions not shown) | |||
Line 148: | Line 148: | ||
<div id="header2" class="container"> | <div id="header2" class="container"> | ||
<p> | <p> | ||
- | <aside class="container" id="ebox1"> <img src="https://static.igem.org/mediawiki/2014hs/b/bb/NGSSlogo.png" alt="" width="198" height="112" id="Image5" /><img src="https://static.igem.org/mediawiki/2014hs/8/82/Bos.png" alt="" width="39" height="91" align="right"/><img src="https://static.igem.org/mediawiki/2014/b/b1/Iitdpage_IGEM_official_logo.png" alt="" width="136" height="88" align="right"/></aside> | + | <aside class="container" id="ebox1"> <a href="https://2014hs.igem.org/Team:NGSS_TR"/><img src="https://static.igem.org/mediawiki/2014hs/b/bb/NGSSlogo.png" alt="" width="198" height="112" id="Image5" /><img src="https://static.igem.org/mediawiki/2014hs/8/82/Bos.png" alt="" width="39" height="91" align="right"/><a href="https://2014hs.igem.org/Main_Page"/><img src="https://static.igem.org/mediawiki/2014/b/b1/Iitdpage_IGEM_official_logo.png" alt="" width="136" height="88" align="right"/></aside> |
</p> | </p> | ||
</div> | </div> | ||
Line 171: | Line 171: | ||
</section> | </section> | ||
</div> | </div> | ||
+ | <p> </p> | ||
+ | <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> |
Latest revision as of 11:34, 20 June 2014
PROTOCOLS
|