Difference between revisions of "Part:BBa K2371011"
 
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The user need to conduct a PCR to linearize the part before reacting with T7 report system.
 
The user need to conduct a PCR to linearize the part before reacting with T7 report system.
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[[File:BGIC-Union Part 123 RFP.png|700px]]
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<h5>Figure 1. The plasmid of pT7-eforRED. pT7-eforRED is composed of a T7 promotor, an RBS and the coding sequence of RFP. This plasmid is used to act as report gene in our report system.</h5>
  
 
We conducted both PCR check(VF and VR) and enzyme check(XbaI and SpeI)
 
We conducted both PCR check(VF and VR) and enzyme check(XbaI and SpeI)
  
 
[[File:Pcr test of eforRed and GFP.png|400px]]
 
[[File:Pcr test of eforRed and GFP.png|400px]]
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<h5>Figure 1.PCR check of eforRed and amliGFP. The expected result of eforRed should be around 1000bp. The insufficient specificity of primers produce another band but the band around 1000bp can present the success of construction. The expected result of amliGFP should be around 1000bp. The control is J23119 biobrick.</h5>
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<h5>Figure 2. PCR check of eforRed and amliGFP. The expected result of eforRed should be around 1000bp. The insufficient specificity of primers produce another band but the band around 1000bp can present the success of construction. The expected result of amliGFP should be around 1000bp. The control is J23119 biobrick.</h5>
  
  
 
[[File:RD test of amliRed and GFP.png|400px]]
 
[[File:RD test of amliRed and GFP.png|400px]]
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<h5>Figure 2.RD check of eforRed and amliGFP. XbaI and SpeI were used. The expected length of both amliGFP and eforRed should be around 750bp.</h5>
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<h5>Figure 3. RD check of eforRed and amliGFP. XbaI and SpeI were used. The expected length of both amliGFP and eforRed should be around 750bp.</h5>
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Latest revision as of 19:59, 1 November 2017


pT7-eforRed


In cell and molecular biology, the eforRed gene is often used as reporter. We add a T7 promotor and a RBS in front of the RFP in order to improve it to be utilized in our paired dCas9 T7 report system in cell free system together with N-t7-dCas9(BBa_K2371000) and C-t7-dCas9(BBa_K2371001).

The user need to conduct a PCR to linearize the part before reacting with T7 report system.

BGIC-Union Part 123 RFP.png

Figure 1. The plasmid of pT7-eforRED. pT7-eforRED is composed of a T7 promotor, an RBS and the coding sequence of RFP. This plasmid is used to act as report gene in our report system.

We conducted both PCR check(VF and VR) and enzyme check(XbaI and SpeI)

Pcr test of eforRed and GFP.png

Figure 2. PCR check of eforRed and amliGFP. The expected result of eforRed should be around 1000bp. The insufficient specificity of primers produce another band but the band around 1000bp can present the success of construction. The expected result of amliGFP should be around 1000bp. The control is J23119 biobrick.


RD test of amliRed and GFP.png

Figure 3. RD check of eforRed and amliGFP. XbaI and SpeI were used. The expected length of both amliGFP and eforRed should be around 750bp.

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