Difference between revisions of "Part:BBa K602008"
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=='''Team Botchan_Lab_Tokyo 2019 characterization'''== | =='''Team Botchan_Lab_Tokyo 2019 characterization'''== | ||
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=='''description'''== | =='''description'''== | ||
Revision as of 18:34, 21 October 2019
D. radiodurans RecA expression device
D. radiodurans RecA with LacI constitutive promoter and ribosome binding site attached upstream. Constitutively expresses RecA. Should increase DNA damage repair capability and radioresistance of host E. coli.
Please see Experience page for characterization details.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 450
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 1124
- 1000COMPATIBLE WITH RFC[1000]
Team Botchan_Lab_Tokyo 2019 characterization
We characterized BBa_K602008.
description
It is RecA (composite parts) that combined the psB1C3 is vector in the basic parts with RecA is the coding parts in an in-fusion cloning. The graph below shows the growth curves of competent cells, DH5α without this plasmid and the composite parts.
This chart is standard deviation (SD) of the technical replicate, and the SD is calculated based on data that originally follow a normal distribution. Therefore, it is necessary to determine whether the data follow a normal distribution by the Shapiro-Wilk test. However, the SD was calculated assuming that all data follow a normal distribution because the number of samples worthy of the Shapiro Wilk test cannot be shake-cultured due to laboratory problems.
conclusion
Competent cells grew as expected.