Difference between revisions of "Part:BBa K4241013"
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===Usage and Biology=== | ===Usage and Biology=== | ||
− | + | The T7 tag is used to increase yield of recombinant protein production. This part also contains thrombin and 6xHis for double His-pulldown purification. | |
It is of note that this seqence does not contain a start codon, therefore to use this part it must be in frame with a promoter with a Met initiation site. | It is of note that this seqence does not contain a start codon, therefore to use this part it must be in frame with a promoter with a Met initiation site. | ||
<br/> | <br/> |
Latest revision as of 11:20, 9 October 2022
6xHis-thrombin-T7Tag
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 55
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Overview
This contains adds the 6xHis-Thrombin-T7 tag. The T7 tag is proven to increase the yield of recombinant protein production, whilst thrombin is used to cleave the 6xHis tag for purification purposes.
Usage and Biology
The T7 tag is used to increase yield of recombinant protein production. This part also contains thrombin and 6xHis for double His-pulldown purification.
It is of note that this seqence does not contain a start codon, therefore to use this part it must be in frame with a promoter with a Met initiation site.
For purification:
1. His-pulldown complete construct
2. Cleave thrombin
3. His-pulldown once again to remove uncleaved product.