Difference between revisions of "Part:BBa K5492011"
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− | + | ===Experiments=== | |
+ | ==PCR - optimised DAO== | ||
+ | We have found the following PCR protocol the most optimal for the part: | ||
+ | https://static.igem.wiki/teams/5492/registry/dao-pcr-plan.png | ||
+ | |||
+ | |||
+ | We added the following substrates in order: | ||
+ | |||
+ | https://static.igem.wiki/teams/5492/registry/dao-pcr-substr.png | ||
+ | |||
+ | |||
+ | We added 6X DNA Loading dye to each PCR tubes. | ||
+ | We loaded the wells of the gels with 12μL of DAO solution in the following order: | ||
+ | |||
+ | |||
+ | |||
+ | https://static.igem.wiki/teams/5492/registry/opt-dao-pcr.png | ||
+ | |||
+ | 1.D31O 2.D32O 3.D33O 4.D34O 5.Ladder | ||
<partinfo>BBa_K5492011 SequenceAndFeatures</partinfo> | <partinfo>BBa_K5492011 SequenceAndFeatures</partinfo> | ||
Latest revision as of 15:03, 1 October 2024
Twist adapter reverse primer
Reverse primer sequence of the adapter sequence utilised by Twist Bioscience. Utilised in PCR reactions for part BBa_K5492202 and BBa_K5492203.
Experiments
PCR - optimised DAO
We have found the following PCR protocol the most optimal for the part:
We added the following substrates in order:
We added 6X DNA Loading dye to each PCR tubes.
We loaded the wells of the gels with 12μL of DAO solution in the following order:
1.D31O 2.D32O 3.D33O 4.D34O 5.Ladder
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]