Difference between revisions of "Part:BBa K578005"

 
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<partinfo>BBa_K578005 short</partinfo>
 
<partinfo>BBa_K578005 short</partinfo>
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<partinfo>BBa_K578005 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K578005 SequenceAndFeatures</partinfo>
  
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===Confirmation of Function===
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This BioBrick was successfully transformed into a variety of vectors, including pSB1C3, pSB1A3, pSB1K3, and Novagen pRSF Duet. Success was evident due to the presence of glowing colonies.
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[[Image: ASU_GFP_Duet.png|400px]]
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===Use in Competent Cells===
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E. Coli MG1655 with this BioBrick in pRSF Duet was successfully made chemically competent using the OWW TSS procedure, allowing for the transformation of a second plasmid.
  
 
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Revision as of 07:01, 3 October 2011

J23102+E0840 (Constitutive GFP)

This is a combination of the GFP coding region (E0840), and the medium strength constitutive promoter, J23102.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 708

Confirmation of Function

This BioBrick was successfully transformed into a variety of vectors, including pSB1C3, pSB1A3, pSB1K3, and Novagen pRSF Duet. Success was evident due to the presence of glowing colonies.

ASU GFP Duet.png

Use in Competent Cells

E. Coli MG1655 with this BioBrick in pRSF Duet was successfully made chemically competent using the OWW TSS procedure, allowing for the transformation of a second plasmid.