Difference between revisions of "Part:BBa K2382010"
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<partinfo>BBa_K2382010 short</partinfo> | <partinfo>BBa_K2382010 short</partinfo> | ||
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+ | <span class='h3bb'>Sequence and Features</span> | ||
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By ligating the constitutive promoter (BBa_J23101), strong ribosome | By ligating the constitutive promoter (BBa_J23101), strong ribosome | ||
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RFP as indicator, and make their own test strip! | RFP as indicator, and make their own test strip! | ||
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+ | <!-- Add more about the biology of this part here | ||
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− | + | ===Usage and Biology=== | |
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<!-- Uncomment this to enable Functional Parameter display | <!-- Uncomment this to enable Functional Parameter display |
Revision as of 16:54, 27 October 2017
Anti-aflatoxin scFv fusion protein construction DNA sequence
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 1342
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 403
Illegal SapI.rc site found at 316
By ligating the constitutive promoter (BBa_J23101), strong ribosome
binding site (BBa_B0034) and scFv-EAAAK- RFP-Histag, we were able to
detect aflatoxin by the purified protein expressing in E. coli. Moreover, we
designed a restriction site, BamHI, between scFv and EAAAK, so future iGEM
teams could take advantage of this composite part to fuse their scFv with
RFP as indicator, and make their own test strip!