Difference between revisions of "Part:BBa K861140:Experience"
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| − | <li>Antisense | + | <li>Antisense CCTGCAGTACTAGTATTACTTCTTAATGCCCATCTCTTCT |
| − | <br/><li> | + | <br/><li>Sense CGAATTCTTCTAGAGATGGCTGCCATTAATACGAAAG |
<br/>After amplifying by PCR, the DNA fragmentation was examined by agarose gel electrophoresis, the lads show that the sizes of the gene were correct. | <br/>After amplifying by PCR, the DNA fragmentation was examined by agarose gel electrophoresis, the lads show that the sizes of the gene were correct. | ||
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Latest revision as of 06:33, 21 September 2012
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how you used this part and how it worked out.
Applications of BBa_K861140
As for the genes we clone, there is no difference between E. coli str. K12 MG1655 and more available DH5α. we purified and amplified these genes from genome of Escherichia coli str. DH5α using PCR. The primers contain the standard restriction enzyme cutting sites. The sequences of the primers used are as below.
After amplifying by PCR, the DNA fragmentation was examined by agarose gel electrophoresis, the lads show that the sizes of the gene were correct.
User Reviews
UNIQe4e4017ef85785c9-partinfo-00000001-QINU UNIQe4e4017ef85785c9-partinfo-00000002-QINU