Difference between revisions of "Part:BBa K3020001:Experience"
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===Applications of BBa_K3020001=== | ===Applications of BBa_K3020001=== | ||
| + | The recA promoter PCR product was electrophoresed and analyzed by a gel imaging system. The results are shown in the figure below and can be seen to be substantially consistent with the expected sequence length. | ||
| + | [[File:RecA pcr production.jpeg|thumb|400px|center | ||
| + | |recA PCR product electropherogram]] | ||
| + | |||
| + | We added green fluorescent protein after the promoter to verify the functionality of the promoter and sensitivity to DNA damage.The plasmid consisting of the RecA promoter and the optimized eGFP fluorescent protein:[https://parts.igem.org/Part:BBa_K3020000 Part:BBa_K3020000]. | ||
===User Reviews=== | ===User Reviews=== | ||
Revision as of 07:14, 8 September 2019
This experience page is provided so that any user may enter their experience using this part.
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how you used this part and how it worked out.
Applications of BBa_K3020001
The recA promoter PCR product was electrophoresed and analyzed by a gel imaging system. The results are shown in the figure below and can be seen to be substantially consistent with the expected sequence length.
We added green fluorescent protein after the promoter to verify the functionality of the promoter and sensitivity to DNA damage.The plasmid consisting of the RecA promoter and the optimized eGFP fluorescent protein:Part:BBa_K3020000.
User Reviews
UNIQe22267b409e4b9a1-partinfo-00000000-QINU UNIQe22267b409e4b9a1-partinfo-00000001-QINU