Difference between revisions of "Part:BBa K511805"
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+ | <partinfo>BBa_K511805 short</partinfo> | ||
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+ | This MammoBlock composite device produces the yellow fluorescent protein EYFP-FF4x4 at a low, constitutive level; in addition, this device can be inhibited by LacI variants. | ||
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+ | <html><img src='https://static.igem.org/mediawiki/2011/0/0d/Specimen_001_Charles_2.fcs_scatter.jpg | ||
+ | ' style="width:60%"><br></html> | ||
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+ | <html><img src='https://static.igem.org/mediawiki/2011/1/12/Specimen_001_Charles_1.fcs_scatter.jpg | ||
+ | ' style="width:60%"><br></html> | ||
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+ | (1A) This scatter plot shows the distribution of the Hek293 population after it was transfected with the following DNA parts: Hef1a-LacO:eYFP and Hef1a:mKate, both of which were constitutively active, expressing yellow and red fluorescent proteins respectively. We observe a distinct shift of approximately 83% of the population in their eYFP fluorescence (FITC channel), while we observe a 69% shift in mKate fluorescence (PE-TexasRed channel). (1C) The negative control sample was transfected with plasmids containing no functional promotor-gene pairs. | ||
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+ | <!-- Add more about the biology of this part here | ||
+ | ===Usage and Biology=== | ||
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+ | <!-- --> | ||
+ | <span class='h3bb'>Sequence and Features</span> | ||
+ | <partinfo>BBa_K511805 SequenceAndFeatures</partinfo> | ||
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+ | |||
+ | <!-- Uncomment this to enable Functional Parameter display | ||
+ | ===Functional Parameters=== | ||
+ | <partinfo>BBa_K511805 parameters</partinfo> | ||
+ | <!-- --> |
Latest revision as of 16:18, 10 May 2013
Repressible Yellow Fluorescence Generator (Hef1a-LacO-EYFP-4xFF4) MammoBlock Device
This MammoBlock composite device produces the yellow fluorescent protein EYFP-FF4x4 at a low, constitutive level; in addition, this device can be inhibited by LacI variants.
(1A) This scatter plot shows the distribution of the Hek293 population after it was transfected with the following DNA parts: Hef1a-LacO:eYFP and Hef1a:mKate, both of which were constitutively active, expressing yellow and red fluorescent proteins respectively. We observe a distinct shift of approximately 83% of the population in their eYFP fluorescence (FITC channel), while we observe a 69% shift in mKate fluorescence (PE-TexasRed channel). (1C) The negative control sample was transfected with plasmids containing no functional promotor-gene pairs.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 416
Illegal PstI site found at 921
Illegal PstI site found at 1502 - 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 292
Illegal PstI site found at 416
Illegal PstI site found at 921
Illegal PstI site found at 1502 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 670
Illegal BamHI site found at 255
Illegal XhoI site found at 1069 - 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 416
Illegal PstI site found at 921
Illegal PstI site found at 1502 - 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 416
Illegal PstI site found at 921
Illegal PstI site found at 1502
Illegal NgoMIV site found at 804
Illegal AgeI site found at 80 - 1000COMPATIBLE WITH RFC[1000]