Difference between revisions of "Part:BBa K3020001:Experience"

(Applications of BBa_K3020001)
 
Line 5: Line 5:
  
 
===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].
 
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].

Latest revision as of 06:04, 21 October 2019


This experience page is provided so that any user may enter their experience using this part.
Please enter how you used this part and how it worked out.

Applications of BBa_K3020001

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

UNIQ4baec0d9ac53f159-partinfo-00000000-QINU UNIQ4baec0d9ac53f159-partinfo-00000001-QINU