Difference between revisions of "Part:BBa K1592002:Experience"

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//In this part, we would like to realize a point mutation. Totally, this sequence includes 2436bp. So we decided to use PCR to mutate. Mutation site locates at 2238 within BBa_K1592002, C->T.Primer forward is cgaggccgctgctggtgctcacgccactgccggtgccattg,and reverse is caatggcaccggcagtggcgtgagcaccagcagcggcctcg.
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Mix include: BM2 2 μl, forward primer 2μl, reverse primer 2μl, H2O 19μ, 2×phanta Max Master Mix25μl.Process includes 95°C for 30s, degradation at 95°C for 15s，annealing at 63°C for 15s, extension at 72°C for 2min, 25cycles,72°C for another 5min.Then run a gel to see whether PCR is successful. Use 5k marker and 1% gel running for 30min. After that, extract DNA sample from gel to get final products. But we cannot make sure whether point mutation happened. So we sent sample to a sequencing company. Fortunately, it’s mutated.
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iGEM18_SUSTech_Shenzhen further characterized this part by repair the point mutation.

Latest revision as of 07:56, 13 October 2018


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UNIQ964cfd44f8dbd343-partinfo-00000000-QINU UNIQ964cfd44f8dbd343-partinfo-00000001-QINU // iGEM18_SUSTech_Shenzhen further characterized this part by repair the point mutation.