Difference between revisions of "Part:BBa K2235006"

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<partinfo>BBa_K2235006 short</partinfo>
 
<partinfo>BBa_K2235006 short</partinfo>
 
<p>
 
<p>
This part constitutes of RBS functional unit attached to sialidase basic part (BBa_K2235005) that can be used to test on various promoters. BBa_K2235007 biobrick has the characterisation for an OmpR promoter fused to this (BBa_K2235006) part. Further, the following parts contain the sialidase enzyme:  
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This part constitutes of RBS functional unit attached to sialidase basic part (BBa_K2235005) that can be used to test on various promoters. BBa_K2235007 biobrick has the characterisation for an OmpR promoter fused to this (BBa_K2235006) part. The following parts contain the sialidase enzyme:  
  
 
<br>Basic part BBa_K2235005 consists of the sialidase enzyme coding sequence with a His tag C-terminally attached.  
 
<br>Basic part BBa_K2235005 consists of the sialidase enzyme coding sequence with a His tag C-terminally attached.  

Revision as of 19:36, 31 October 2017


Sialidase enzyme with a RBS attached

This part constitutes of RBS functional unit attached to sialidase basic part (BBa_K2235005) that can be used to test on various promoters. BBa_K2235007 biobrick has the characterisation for an OmpR promoter fused to this (BBa_K2235006) part. The following parts contain the sialidase enzyme:
Basic part BBa_K2235005 consists of the sialidase enzyme coding sequence with a His tag C-terminally attached.
BBa_K2235009 biobrick is a composite of a T7 promoter and RBS followed by sialidase with characterisation data of the enzyme.
BBa_K2235011 is a conjugation of sialidase composite (BBa_K2235009) with a device that facilitates the secretion of the enzyme out of the E.coli bacterial cell.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal XhoI site found at 73
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 520
    Illegal NgoMIV site found at 595
    Illegal NgoMIV site found at 685
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 1065