JeffHusdsz (Talk | contribs) |
JeffHusdsz (Talk | contribs) |
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+ | <h2>Transfection </h2> | ||
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+ | <p style="color:black;font-size:35px;"> | ||
+ | The plasmid was diluted 1000-fold and 10000-fold, and the competent bacteria BL-21 was added for 30 minutes in an ice bath. Then we heated the bacteria at 42 degrees for one minute, and ice-bathed for five more minutes. After that, we added 400 ml of LB without Kana antibiotic and shook the bacterial fluid. Finally, the bacteria were sprayed on a petri dish with kana antibiotics. | ||
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+ | <h2>Bacterial Fluid PCR to filter positive clones</h2> | ||
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+ | <p style="color:black;font-size:35px;">To insure the plasmids were successfully transfected, we conducted bacterial fluid PCR. | ||
+ | Our groupmates take ten 1.5 ml EP tubes, add 200 μl of kana resistant medium separately, directly draw a single clone with a small pipette tip and push the TIP directly into an EP tube. We covered the EP tube and shake the bacteria at 37 degrees for 2-3 hours. Then 1μl of the bacterial solution was used as a template to identify the PCR positive clone. DNA gel electrophoresis was used to see if there was a target strip to judge. | ||
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Revision as of 14:29, 17 October 2018