Difference between revisions of "Part:BBa K5392019"
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<partinfo>BBa_K5392019 short</partinfo> | <partinfo>BBa_K5392019 short</partinfo> | ||
− | + | ==Description== | |
+ | To obtain the desired saturation mutagenesis, oligonucleotide primers were designed with degenerate codons. In addition, each single-site saturation mutant was generated according to the PCR-based QuickChange method. The PCR was performed according to the operation manual. The PCR product was digested with DpnI restriction enzyme and transformed into E.coli DH5-alpha competent cells.We will extract the plasmid and sequence it to make sure the mutation was successful. | ||
+ | |||
+ | <html><style> | ||
+ | img{margin:auto;} | ||
+ | #a1{width:324px;height:317px;margin:auto;border:3px solid grey} | ||
+ | |||
+ | </style><div id="a1"> | ||
+ | <img src="https://static.igem.wiki/teams/5392/pet28a-zatdt-r335f-page.png" width="324" height="315"/> | ||
+ | </div></html> | ||
+ | |||
+ | ==Experiment== | ||
+ | ===<strong>SDS-PAGE of ZaTdT-R335F</strong>=== | ||
+ | We transfected the Sequencing is correct ZaTdT-R335F plasmid into E.coli BL21(DE3) competent cell. After overnight, an appropriate colony was used to express the mutant protein and verify its activity | ||
+ | |||
+ | <html><style> | ||
+ | img{margin:auto;} | ||
+ | #a2{width:370px;height:208px;margin:auto;border:3px solid grey} | ||
+ | |||
+ | </style><div id="a2"> | ||
+ | <img src="https://static.igem.wiki/teams/5392/zatdt-r335f.png" width="366" height=204""/> | ||
+ | </div></html> | ||
+ | |||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 06:23, 29 September 2024
Vector-ZaTdT-R335F-KanR
Description
To obtain the desired saturation mutagenesis, oligonucleotide primers were designed with degenerate codons. In addition, each single-site saturation mutant was generated according to the PCR-based QuickChange method. The PCR was performed according to the operation manual. The PCR product was digested with DpnI restriction enzyme and transformed into E.coli DH5-alpha competent cells.We will extract the plasmid and sequence it to make sure the mutation was successful.
Experiment
SDS-PAGE of ZaTdT-R335F
We transfected the Sequencing is correct ZaTdT-R335F plasmid into E.coli BL21(DE3) competent cell. After overnight, an appropriate colony was used to express the mutant protein and verify its activity
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]
- 1000COMPATIBLE WITH RFC[1000]