Difference between revisions of "Part:BBa K782073"
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==Introduction==
 
==Introduction==
  
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Our construct contain [https://parts.igem.org/Part:BBa_K782069 TALA and TALB binding sites], which are adjacent to each. For that reason two different TAL regulators are unable to bind to its binding sites at once because of steric interference. TAL binding sites are cloned downstream of CMV promoter. Upstream  of CMV is Blue fluorescent protein. BFP in a monomeric fluorescent protein with excitation maximum at 402 nm and emision maximum at 457 nm.
+
Our construct contain [https://parts.igem.org/Part:BBa_K782069 TALA and TALB binding sites], which are adjacent to each other. Because of steric interference two different TAL regulators are unable to bind to its binding sites at once. TAL binding sites are cloned downstream of CMV promoter. Upstream  of CMV is Blue fluorescent protein. BFP is a monomeric fluorescent protein with excitation maximum at 402 nm and emision maximum at 457 nm.
  
 
[[Image:Abbfp.png‎]]
 
[[Image:Abbfp.png‎]]

Revision as of 19:46, 25 September 2012

10x[TALA+TALB] operator_CMV promoter_BFP

Introduction

Our construct contain TALA and TALB binding sites, which are adjacent to each other. Because of steric interference two different TAL regulators are unable to bind to its binding sites at once. TAL binding sites are cloned downstream of CMV promoter. Upstream of CMV is Blue fluorescent protein. BFP is a monomeric fluorescent protein with excitation maximum at 402 nm and emision maximum at 457 nm.

Abbfp.png

Figure 1: Schematic representation of the construct.


Characterization

Results:

BFP was obtained from Evrogen.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 730
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 149
    Illegal NgoMIV site found at 514
    Illegal AgeI site found at 12
    Illegal AgeI site found at 352
    Illegal AgeI site found at 377
    Illegal AgeI site found at 717
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 1406
    Illegal BsaI.rc site found at 2062