| Line 216: | Line 216: | ||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
<div id="week17"> | <div id="week17"> | ||
| − | + | <p><h5><B>Week 17</B></h5></p> | |
| − | + | <p><h3><B>September 26, 2016:</B></h3></p> | |
| − | <p><h3><B>September 26, 2016 : </B></h3 | + | |
<p> | <p> | ||
| − | <a href="#exp1"><h4> | + | <a href="#exp1"><h4> 248. 248. Purification of the protein </h4></a></br> |
</p> | </p> | ||
| − | + | ||
248. 248. Purification of the protein
Aim: Purifying the protein C2 produced by BL21(DE3) using a Fast Purification Liquid Chromatography. What we did in the lab: Materials: • Fast Purification Liquid Chromatography • Chaotropic reagent (Guanidinium 6M) • EDTA 0,1M • PMSF (100mM) • Ni 2+ solution (100mM) • Centrifuge • Buffer A (50mM Tris, 150mM of NaCl) • Buffer B (50mM Tris, 150mM of NaCl, 250mM Imidazole, pH=7.4) Method: Melt the pellet of bacteria C2 (from 1L culture) and resuspend it with 10ml of buffer A. We had 25ml of pellet we complete until 40ml with buffer A. Add 40 µL of PMSF to avoid protein denaturation. Put the column on the FPLC, clean the FPLC with water and then fill it with buffer A. Sonicate the sample three times one minute at 60%, wait 90 seconds between each sonication. Centrifuge 25 min at 16000g (rotor JA 25.50) Inject your sample in the FPLC Get back several samples: • C: Crude extract : before centrigugation • P: Pellet • SN: Supernatant • F: Flow through (unfixed proteins) • W: Wash 5% of buffer B • Fractions (depending on the gradient)
