Difference between revisions of "Part:BBa K2040100:Experience"
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===Applications of BBa_K2040100=== | ===Applications of BBa_K2040100=== | ||
− | We used primer | + | We used |
+ | forward primer | ||
5' ACGTCCTGCAGAATCATGCAGCGCTATGAG 3' | 5' ACGTCCTGCAGAATCATGCAGCGCTATGAG 3' | ||
+ | & reverse primer | ||
5' ATAAGCGGCCGCCATGATGGTCTAGGGAACG 3' | 5' ATAAGCGGCCGCCATGATGGTCTAGGGAACG 3' | ||
− | to | + | to extract PMcl1 and its 5' untranslated region (99bp downstream the promoter) from genomic DNA of ''Metarhizium anisopliae''. The whole length is 2772bp. |
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+ | [[Image:PMcl1_PCR.png|left|250px|thumb|Figure1. Amplify PMcl1 from gDNA]] | ||
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+ | Then we digested the DNA fragment with NotI and PstI in order to insert it into the backbone. However, when we ran gel electrophoresis to check the digestion result, we found that there is still one PstI restriction site inside the PMcl1 whcih is the one we did not know when we designed. | ||
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===User Reviews=== | ===User Reviews=== |
Revision as of 07:42, 16 October 2016
Applications of BBa_K2040100
We used forward primer 5' ACGTCCTGCAGAATCATGCAGCGCTATGAG 3' & reverse primer 5' ATAAGCGGCCGCCATGATGGTCTAGGGAACG 3' to extract PMcl1 and its 5' untranslated region (99bp downstream the promoter) from genomic DNA of Metarhizium anisopliae. The whole length is 2772bp.
Then we digested the DNA fragment with NotI and PstI in order to insert it into the backbone. However, when we ran gel electrophoresis to check the digestion result, we found that there is still one PstI restriction site inside the PMcl1 whcih is the one we did not know when we designed.
User Reviews
UNIQ1815cbfe85b395bc-partinfo-00000000-QINU UNIQ1815cbfe85b395bc-partinfo-00000001-QINU