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<div class="blog_top"> | <div class="blog_top"> | ||
<h4 class="blog_topHd"> | <h4 class="blog_topHd"> | ||
− | Competent cells: E.Coli | + | Competent cells: E.Coli BL21</h4> |
</div> | </div> | ||
<h4 class="blog_topHd">Objectives</h4> | <h4 class="blog_topHd">Objectives</h4> | ||
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<h3> Stock concentrations:</h3> | <h3> Stock concentrations:</h3> | ||
− | <li><p>O/N BL21 pre-culture: O/N inoculation of 100 µL | + | <li><p>O/N BL21 pre-culture: O/N inoculation of 100 µL BL21 into 100 mL LB.</p> |
</li> | </li> | ||
<li><p>0.1M CaCl2: prepared the 05/06</p> | <li><p>0.1M CaCl2: prepared the 05/06</p> |
Revision as of 09:45, 12 October 2016
The objective here is to make a stock of E.Coli BL21 competent cells for subsequent transformations. O/N BL21 pre-culture: O/N inoculation of 100 µL BL21 into 100 mL LB. 0.1M CaCl2: prepared the 05/06 0.1M CaCl2/15% Glycerol: prepared the 05/06 Inoculation of 3 mL O/N culture in 100 mL LB in 500 mL erlenmeyer. Incubation at 250 rpm at 37°C until the DO 0,6 —> DO = 0.615 Cells were transferred to 3 sterile ice-cold 50 mL Falcon tubes. 20 mL in each falcon tube. Incubate on ice for 30 min. Do not allow cells to warm up over 4°C. Spin cells at 4000 rpm for 10 min at 4°C. Discard supernatant and try to drain all remaining media. Gently resuspend on 10 mL cold 0.1M CaCl2 Incubate on ice 20 min Centrifuge 10 min at 4,000 rpm at 4°C Discard supernatant and gently resuspend on 5 mL cold 0.1M CaCl2/25% Glycerol Transfer in 1.5 mL eppendorf (100 µL/tube) Store at -80°C NB: The competency of the prepared cells will be tested the 10/06.
Competent cells: E.Coli BL21
Objectives
Materials
Stock concentrations:
Protocol
Competence: