Team:Bielefeld-Germany/Results/S-Layer/Guide/5

From 2011.igem.org

(Difference between revisions)
Line 13: Line 13:
<img id="Image-Maps_8201110281849269" src="https://static.igem.org/mediawiki/2011/c/c0/Navigationbar.png" usemap="#Image-Maps_8201110281849269" border="0" width="535" height="82" alt="" />
<img id="Image-Maps_8201110281849269" src="https://static.igem.org/mediawiki/2011/c/c0/Navigationbar.png" usemap="#Image-Maps_8201110281849269" border="0" width="535" height="82" alt="" />
<map id="_Image-Maps_8201110281849269" name="Image-Maps_8201110281849269">
<map id="_Image-Maps_8201110281849269" name="Image-Maps_8201110281849269">
-
<area shape="rect" coords="22,12,170,62" href="https://2011.igem.org/Team:Bielefeld-Germany/Results/S-Layer/Guide/2" alt="Previous page" title="Previous page"    />
+
<area shape="rect" coords="22,12,170,62" href="https://2011.igem.org/Team:Bielefeld-Germany/Results/S-Layer/Guide/2" alt="Jump to intersection" title="Jump to intersection"    />
<area shape="rect" coords="182,7,330,57" href="https://2011.igem.org/wiki/index.php?title=Team:Bielefeld-Germany/Results/S-Layer/Guide" alt="Return to beginning" title="Return to beginning"    />
<area shape="rect" coords="182,7,330,57" href="https://2011.igem.org/wiki/index.php?title=Team:Bielefeld-Germany/Results/S-Layer/Guide" alt="Return to beginning" title="Return to beginning"    />
<area shape="rect" coords="353,10,501,60" href="https://2011.igem.org/Team:Bielefeld-Germany/Results/S-Layer/Guide/6" alt="Next page" title="Next page"    />
<area shape="rect" coords="353,10,501,60" href="https://2011.igem.org/Team:Bielefeld-Germany/Results/S-Layer/Guide/6" alt="Next page" title="Next page"    />

Revision as of 00:28, 29 October 2011

Filtration of the cell lysate

A Milipore Pellicon XL 300 membrane actuated with a SciLog TANDEM 1081 peristaltic pump.

Centrifugation does not remove all of the cell debris, therefore a tangential flow ultrafiltration step with a 300 kDa membrane is performed. The retentate is collected. Instead of this device you can also use a simple dead-end sterile filter (0.22 µm poresize) but it is easier the way described above (the dead-end filter gets clogged after some time...).

With the cleared lysate the histidine affinity tag comes into play - want to know how?

Jump to intersection Return to beginning Next page