Difference between revisions of "Part:BBa K3038000:Experience"
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| − | PCR amplification of the PCR products | + | ===PCR amplification of the PCR products=== |
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| − | Plasmid construction | + | ===Plasmid construction=== |
https://2019.igem.org/wiki/images/5/5b/T--Poitiers--plasmid_construction_ADR-tab3.jpg | https://2019.igem.org/wiki/images/5/5b/T--Poitiers--plasmid_construction_ADR-tab3.jpg | ||
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| − | Expression of the CMYC-6HIS-ADR and ADR-CMYC-6HIS recombinant proteins | + | ===Expression of the CMYC-6HIS-ADR and ADR-CMYC-6HIS recombinant proteins=== |
https://2019.igem.org/wiki/images/6/67/T--Poitiers--recombinantexpression_ADR-tab3.png | https://2019.igem.org/wiki/images/6/67/T--Poitiers--recombinantexpression_ADR-tab3.png | ||
| + | After sequencing, induction was performed on the thermocompetent bacteria JM109. The objective was to verify if the cloned gene leads to the production of a protein. The expected size of the ADR protein is 40 kDa. A very strong expression of the ADR protein was observed at this size when the pBAD promoter is induced with arabinose. The gene has therefore been correctly cloned into the strain and the protein is produced. | ||
| − | Activity | + | ===Activity=== |
===User Reviews=== | ===User Reviews=== | ||
Revision as of 09:21, 10 October 2019
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how you used this part and how it worked out.
Applications of BBa_K3038000
PCR amplification of the PCR products
Electrophoresis photography following deposits on agarose gel 0.8% of enzymatic digestion products. The migration was performed at 100 volts for 30 minutes in TAE 1X. The marker used during the migration is the NEB 1 kb Plus Ladder. Lane 1 corresponds to the marker, lane 2 to the digested N-ter,ADR lane 3 to the digested C-ter ADR and lane 4 to the digested plasmid pSB1A3.
Plasmid construction
Design of ADR N-ter/pSB1A3 and ADR C-ter/pSB1A3 with Geneious software. This map shows the pBAD promoter and its terminator flanking the coding sequence of the ADR protein. Also present in N-ter or C-ter are 6-His and c-myc tag. Finally, in the plasmid is present and ampicillin resistance cassette.
Expression of the CMYC-6HIS-ADR and ADR-CMYC-6HIS recombinant proteins
After sequencing, induction was performed on the thermocompetent bacteria JM109. The objective was to verify if the cloned gene leads to the production of a protein. The expected size of the ADR protein is 40 kDa. A very strong expression of the ADR protein was observed at this size when the pBAD promoter is induced with arabinose. The gene has therefore been correctly cloned into the strain and the protein is produced.
Activity
User Reviews
UNIQ39767eac80570ae2-partinfo-00000000-QINU UNIQ39767eac80570ae2-partinfo-00000001-QINU