Difference between revisions of "Part:BBa K1758101:Design"
m (→Design Notes) |
m |
||
Line 1: | Line 1: | ||
− | |||
__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K1758101 short</partinfo> | <partinfo>BBa_K1758101 short</partinfo> | ||
Line 11: | Line 10: | ||
===Source=== | ===Source=== | ||
− | This part was created by shortening | + | This part was created by shortening [https://parts.igem.org/Part:BBa_I746909 BBa_I746909] and simultaneously adding 5'-UTR via Gibson primers. |
'''Amplification with Gibson-primers:''' | '''Amplification with Gibson-primers:''' |
Revision as of 16:26, 17 August 2015
Translation enhancing 5-UTR + sfGFP
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 SapI.rc site found at 59
Design Notes
[http://www.ncbi.nlm.nih.gov/pubmed/23654270 Lentini et al. 2013] showed that the scar which is created by standard biobrick assembly is disadvantageous for in vitro translation when occuring between RBS and start codon. Therefore we changed the sequence between RBS and start codon for other parts.
Source
This part was created by shortening BBa_I746909 and simultaneously adding 5'-UTR via Gibson primers.
Amplification with Gibson-primers: