Difference between revisions of "Part:BBa K2680265"
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<partinfo>BBa_K2680265 short</partinfo> | <partinfo>BBa_K2680265 short</partinfo> | ||
− | 3G sfCFP-pdt3 | + | 3G sfCFP-pdt3 coding sequence flanked by prefix sticky end C and suffix sticky end D in a 3G-compatible backbone. For more information on 3G hybrid DNA assembly and 3G parts, see the [http://2018.igem.org/Team:William_and_Mary/Part_Collection William and Mary 3G Parts Page]. |
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+ | Superfolding cyan fluorescent protein variant. Similar to <partinfo>BBa_K1093002</partinfo>. | ||
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+ | "Superfolder Cyan Fluorescent Protein is a derivative of superfolder Green Fluorescent protein. Compared to CFP it displays improved stability and strong cyan fluorescence. Excitation peak: 425 nm Emission peak: 475 nm" <sup>1</sup> | ||
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+ | ===References=== | ||
+ | <sup>1</sup>Miścicka, A. (2013, September 20). Part:BBa_K1093002. Retrieved October 16, 2018, from https://parts.igem.org/Part:BBa_K1093002 | ||
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<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Latest revision as of 21:03, 16 October 2018
3G sfCFP-pdt3
3G sfCFP-pdt3 coding sequence flanked by prefix sticky end C and suffix sticky end D in a 3G-compatible backbone. For more information on 3G hybrid DNA assembly and 3G parts, see the [http://2018.igem.org/Team:William_and_Mary/Part_Collection William and Mary 3G Parts Page].
Superfolding cyan fluorescent protein variant. Similar to BBa_K1093002.
"Superfolder Cyan Fluorescent Protein is a derivative of superfolder Green Fluorescent protein. Compared to CFP it displays improved stability and strong cyan fluorescence. Excitation peak: 425 nm Emission peak: 475 nm" 1
References
1Miścicka, A. (2013, September 20). Part:BBa_K1093002. Retrieved October 16, 2018, from https://parts.igem.org/Part:BBa_K1093002
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 47
Illegal BsaI.rc site found at 861
Illegal SapI.rc site found at 67