Difference between revisions of "Part:BBa K3038000:Experience"
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| − | [[Image:T--Poitiers--PCR_amplification_ADR-tab3.jpg|400px. 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. | + | [[Image:T--Poitiers--PCR_amplification_ADR-tab3.jpg|400px|thumb|right|. 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. |
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Revision as of 08:32, 10 October 2019
This experience page is provided so that any user may enter their experience using this part.
Please enter
how you used this part and how it worked out.
Applications of BBa_K3038000
PCR amplification of the PCR products
File:T--Poitiers--PCR amplification ADR-tab3.jpg
. 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
Expression of the recombinant protein
Activity
User Reviews
UNIQ4427c922c8baa3b3-partinfo-00000000-QINU UNIQ4427c922c8baa3b3-partinfo-00000001-QINU