Difference between revisions of "Part:BBa K4164997"
 
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<partinfo>BBa_K4164997 short</partinfo>
 
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This part includes the ddRFPB1 fused by a 3*GS Linker to the RXR , which can form a heterodimer with activated FXR-3*GS Linker-ddRFPA1 and exhibit red fluorescence.
 
This part includes the ddRFPB1 fused by a 3*GS Linker to the RXR , which can form a heterodimer with activated FXR-3*GS Linker-ddRFPA1 and exhibit red fluorescence.
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We tried to determine the solubility of RXR-ddRFPB1 by purifying 6xHis-tagged proteins under native conditions and performing SDS-PAGE to compare the abundance of the band with the size of interest.As shown in the Figure 1, RXR-ddRFPB1(78.9kDa) is soluble and can be purified by Ni-NTA affinity chromatography.
 
We tried to determine the solubility of RXR-ddRFPB1 by purifying 6xHis-tagged proteins under native conditions and performing SDS-PAGE to compare the abundance of the band with the size of interest.As shown in the Figure 1, RXR-ddRFPB1(78.9kDa) is soluble and can be purified by Ni-NTA affinity chromatography.
  
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<p style="text-align: center;"><b>Fig.1 Purification of FXR-ddRFPA1 and RXR-ddRFPB1.Lane 1: protein contained in the pellet after bacterial disruption. Lane 2: RXR-ddRFPB1 purified from supernatant of bacteria liquid. Lane 3: FXR-ddRFPA1 purified from supernatant of bacteria liquid in optimized expression conditon..</b></p>
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<p style="text-align: center;"><b>Fig.1 Purification of FXR-ddRFPA1 and RXR-ddRFPB1.Lane 1: protein contained in the pellet after bacterial disruption. Lane 2: RXR-ddRFPB1 purified from supernatant of bacteria liquid. Lane 3: FXR-ddRFPA1 purified from supernatant of bacteria liquid in optimized expression conditon.</b></p>
  
 
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Latest revision as of 11:57, 12 October 2022


RXR-3*GS Linker-ddRFPB1


This part includes the ddRFPB1 fused by a 3*GS Linker to the RXR , which can form a heterodimer with activated FXR-3*GS Linker-ddRFPA1 and exhibit red fluorescence.

We tried to determine the solubility of RXR-ddRFPB1 by purifying 6xHis-tagged proteins under native conditions and performing SDS-PAGE to compare the abundance of the band with the size of interest.As shown in the Figure 1, RXR-ddRFPB1(78.9kDa) is soluble and can be purified by Ni-NTA affinity chromatography.

Fig.1 Purification of FXR-ddRFPA1 and RXR-ddRFPB1.Lane 1: protein contained in the pellet after bacterial disruption. Lane 2: RXR-ddRFPB1 purified from supernatant of bacteria liquid. Lane 3: FXR-ddRFPA1 purified from supernatant of bacteria liquid in optimized expression conditon.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1867
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 357
    Illegal AgeI site found at 1384
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 739