Difference between revisions of "Part:BBa K2371011"

Line 3: Line 3:
 
<partinfo>BBa_K2371011 short</partinfo>
 
<partinfo>BBa_K2371011 short</partinfo>
  
 +
This chromoprotein eforRed naturally exhibits red/pink color when expressed. The color is slightly weaker than RFP. On agar plates and in liquid culture, the color is readily visible to naked eye in less than 24 hours of incubation. The DNA was codon-optimized for expression in E.coli and synthesized by the Korean company Bioneer Corporation.
  
 
+
<h5>Figure1.PCR test of eforRed and GFP.</h5>
In cell and molecular biology, the GFP gene is frequently used as a reporter of expression.It has been used in modified forms to make biosensors, and many animals have been created that express GFP, which demonstrates a proof of concept that a gene can be expressed throughout a given organism, in selected organs, or in cells of interest.
+
 
+
<h5>Figure1.PCR test of eforRed and amliGFP</h5>
+
  
 
[[File:Pcr test of eforRed and GFP.png|400px]]
 
[[File:Pcr test of eforRed and GFP.png|400px]]
  
<h5>Figure2.RD test of eforRed and amlGFP.</h5>
+
<h5>Figure2.RD test of eforRed and GFP.</h5>
  
 
[[File:RD test of amliRed and GFP.png|400px]]
 
[[File:RD test of amliRed and GFP.png|400px]]

Revision as of 15:29, 31 October 2017


pT7-eforRed

This chromoprotein eforRed naturally exhibits red/pink color when expressed. The color is slightly weaker than RFP. On agar plates and in liquid culture, the color is readily visible to naked eye in less than 24 hours of incubation. The DNA was codon-optimized for expression in E.coli and synthesized by the Korean company Bioneer Corporation.

Figure1.PCR test of eforRed and GFP.

Pcr test of eforRed and GFP.png

Figure2.RD test of eforRed and GFP.

RD test of amliRed and GFP.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
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 689