Difference between revisions of "Part:BBa K1628003"

 
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<partinfo>BBa_K1628003 short</partinfo>
 
<partinfo>BBa_K1628003 short</partinfo>
  
Promoter BJ27UP is an artificially synthesized promoter. We have validate this part through promoter strength assay using bgaB (encoding β-galatosidase downstream of the multiple cloning sites) as reporter genes. According to promoter strength assay in ''B. amyloliquefaciens'' NK-1 (showed in Figure 1), the strength of BJ27UP is stronger than Pbca but is still too weak compared with other promoters.
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Promoter BJ27UP is an artificially synthesized promoter. We have validate this part through promoter strength assay using ''bgaB'' (encoding β-galatosidase downstream of the multiple cloning sites) as reporter gene. According to promoter strength assay in ''B. amyloliquefaciens'' NK-1 (showed in Figure 1), the strength of BJ27UP is stronger than Pbca but is still too weak compared with other promoters.
  
[[File:promoter3_NK.png]]
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[[File:promoter4_NK.png]]
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Latest revision as of 09:04, 18 September 2015

BJ27UP

Promoter BJ27UP is an artificially synthesized promoter. We have validate this part through promoter strength assay using bgaB (encoding β-galatosidase downstream of the multiple cloning sites) as reporter gene. According to promoter strength assay in B. amyloliquefaciens NK-1 (showed in Figure 1), the strength of BJ27UP is stronger than Pbca but is still too weak compared with other promoters.

Promoter4 NK.png

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]