Difference between revisions of "Part:BBa K3286207"
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This part is similar to part <partinfo>BBa_K3286206</partinfo>, but in this strategy, only the transmembrane domain (TMD) was used to fuse with sfGFP. So again, this part was constructed to test whether part <partinfo>BBa_K3286200</partinfo> was getting transcribed, translated and transported to the membrane.
 
This part is similar to part <partinfo>BBa_K3286206</partinfo>, but in this strategy, only the transmembrane domain (TMD) was used to fuse with sfGFP. So again, this part was constructed to test whether part <partinfo>BBa_K3286200</partinfo> was getting transcribed, translated and transported to the membrane.
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[[File:T--Wageningen UR--rpfC-GFP 3 IJ H.jpg|thumb|center|<b>Figure 1:</b> Transformation of this part in <i>E. coli</i> Dh5-Alpha cells incubated on a LB agar plate. Fluorescence is visualized by a fluorescence microscope.]]
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[[File:T--Wageningen UR--rpfC-GFP 3 IJ I.jpg|750px|thumb|center|<b>Figure 1:</b> Transformation of this part in <i>E. coli</i> Dh5-Alpha cells incubated on a LB agar plate. Fluorescence is visualized by a fluorescence microscope.]]
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Figure 1 and 2 are showing the observed fluorescence by this part. What can be observed is that cells are actually showing a higher intensity of fluorescence at the edges. Indicating that this part (but also <partinfo>K3286200</partinfo>) is getting transcribed, translated and transported to the membrane.
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<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Revision as of 08:38, 21 October 2019


RpfCch (TMD) sfGFP fusion

This part is similar to part BBa_K3286206, but in this strategy, only the transmembrane domain (TMD) was used to fuse with sfGFP. So again, this part was constructed to test whether part BBa_K3286200 was getting transcribed, translated and transported to the membrane.

Figure 1: Transformation of this part in E. coli Dh5-Alpha cells incubated on a LB agar plate. Fluorescence is visualized by a fluorescence microscope.
Figure 1: Transformation of this part in E. coli Dh5-Alpha cells incubated on a LB agar plate. Fluorescence is visualized by a fluorescence microscope.

Figure 1 and 2 are showing the observed fluorescence by this part. What can be observed is that cells are actually showing a higher intensity of fluorescence at the edges. Indicating that this part (but also BBa_K3286200) is getting transcribed, translated and transported to the membrane.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 227
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 661
  • 1000
    COMPATIBLE WITH RFC[1000]