Difference between revisions of "Team:UiOslo Norway/Experiments/Solubility Assay"
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<p></br></p> | <p></br></p> | ||
+ | <h3> Cell lysis using glass beads </h3> | ||
<p> | <p> | ||
<ul> | <ul> | ||
− | <li><p>Resuspend cell pellet in 600 | + | <li><p>Resuspend cell pellet in 600 µl PBS buffer (pH 7.4) </p></li> |
<li><p>Add glass beads and disrupt cells by vortexing</p></li> | <li><p>Add glass beads and disrupt cells by vortexing</p></li> | ||
<li><p>Centrifuge at 16.000 x g for 5 minutes</p></li> | <li><p>Centrifuge at 16.000 x g for 5 minutes</p></li> | ||
<li><p>Transfer soluble fraction into a new tube and resuspend insoluble fraction in 600 ul PBS buffer (pH 7.4)</p></li> | <li><p>Transfer soluble fraction into a new tube and resuspend insoluble fraction in 600 ul PBS buffer (pH 7.4)</p></li> | ||
</p> | </p> | ||
+ | </ul> | ||
+ | <h3> Cell lysis using sonication </h3> | ||
+ | |||
+ | <p> | ||
+ | <ul> | ||
+ | <li><p>Resuspend the cell pellet in precooled imidazolebuffer. </p></li> | ||
+ | <li><p>Sonicate 3x for 30 sec at a amplitude of 60. Incubate on ice for 1 minute between each sanitation step.</p></li> | ||
+ | <li><p>Centrifuge the cell lysate at 13.000 rpm for 30 minutes at 4 °C.</p></li> | ||
+ | <li><p>Keep the supernatant for further experiments</p></li> | ||
+ | </p> | ||
+ | <p><b>Imidazole buffer</b></br> | ||
+ | </br> | ||
+ | 50 mM Tris-HCl pH 8 </br> | ||
+ | 100 mM NaCl</br> | ||
+ | 10 mM beta-Mercaptoethanol</br> | ||
+ | 10 mM Imidazole </br> | ||
+ | |||
<div class="clear"></div> | <div class="clear"></div> |
Revision as of 12:07, 10 September 2015
Solubility Assay:
Back to ProtocolsCell lysis using glass beads
Resuspend cell pellet in 600 µl PBS buffer (pH 7.4)
Add glass beads and disrupt cells by vortexing
Centrifuge at 16.000 x g for 5 minutes
Transfer soluble fraction into a new tube and resuspend insoluble fraction in 600 ul PBS buffer (pH 7.4)
Cell lysis using sonication
Resuspend the cell pellet in precooled imidazolebuffer.
Sonicate 3x for 30 sec at a amplitude of 60. Incubate on ice for 1 minute between each sanitation step.
Centrifuge the cell lysate at 13.000 rpm for 30 minutes at 4 °C.
Keep the supernatant for further experiments
Imidazole buffer 50 mM Tris-HCl pH 8 100 mM NaCl 10 mM beta-Mercaptoethanol 10 mM Imidazole