Difference between revisions of "Part:BBa K2100011:Experience"

(Applications of BBa_K2100011)
(Applications of BBa_K2100011)
 
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https://static.igem.org/mediawiki/parts/c/c8/T--MIT--hEF1a.png
 
https://static.igem.org/mediawiki/parts/c/c8/T--MIT--hEF1a.png
  
Here is an image of HEK293 cells constitutively expressing eYFP florescence under a hEF1a promoter. We often used yellow florescence as either a reporter for how our promoter responded to induction in cells or as transfection markers for experiments.  
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Here is an image of HEK293 cells constitutively expressing eYFP florescence under the hEF1a promoter.
  
 
https://static.igem.org/mediawiki/parts/thumb/4/49/T--MIT--khb_eYFPexpression_hek.jpeg/796px-T--MIT--khb_eYFPexpression_hek.jpeg
 
https://static.igem.org/mediawiki/parts/thumb/4/49/T--MIT--khb_eYFPexpression_hek.jpeg/796px-T--MIT--khb_eYFPexpression_hek.jpeg

Latest revision as of 19:02, 21 October 2016


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Applications of BBa_K2100011

The MIT iGEM team used the hEF1a promoter to constitutively express fluorescent proteins as transfection markers in our experiments in HEK293, tHESC, MCF-7, and ISH cells. The amount of fluorescent units observed is an indication of the number of plasmids a particular cell uptakes. The graph below shows two single color controls from one of our experiments. We transfected one well of HEK293 cells with hEF1a-mKate and another with hEF1a-eYFP. The cells that uptook the hEF1a-mKate plasmids showed an increase in only the red fluorescent output, while the cells that uptook the hEF1a-eYFP plasmids showed a clear increase in only the yellow fluorescent output.

T--MIT--hEF1a.png

Here is an image of HEK293 cells constitutively expressing eYFP florescence under the hEF1a promoter.

796px-T--MIT--khb_eYFPexpression_hek.jpeg

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