Difference between revisions of "Part:BBa K5492021"

 
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<span class='h3bb'>Sequence and Features</span>
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===Experiments===
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==PCR – HNMT==
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We have found the following PCR protocol the most optimal for the part:
 +
https://static.igem.wiki/teams/5492/registry/hnmt-pcr-plan.png
 +
 
 +
According to the previous PCR reaction we decided to use S1 and N1 (from our previous
 +
reactions.)
 +
We added the following substrates in order: (each optimized and wild type)
 +
 
 +
https://static.igem.wiki/teams/5492/registry/hnmt-pcr-substr1.png
 +
 
 +
We added 6X DNA Loading dye to each PCR tubes.
 +
We loaded the wells of the gels with 12μL of DNA solution in the following order: 
 +
 
 +
https://static.igem.wiki/teams/5492/registry/hnmt-pcr.png
 +
1. S1O (optimized)
 +
2. S1W (wild type)
 +
3. N1O (optimized)
 +
4. N1W (wild type)
 +
5. Ladder
 
<partinfo>BBa_K5492021 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K5492021 SequenceAndFeatures</partinfo>
  

Latest revision as of 11:37, 2 October 2024


Genscript adapter reverse primer

Reverse primer sequence of the adapter sequence utilised by GenScript. Utilised in PCR reactions for part BBa_K5492402 and BBa_K5492403.


Experiments

PCR – HNMT

We have found the following PCR protocol the most optimal for the part: hnmt-pcr-plan.png

According to the previous PCR reaction we decided to use S1 and N1 (from our previous reactions.) We added the following substrates in order: (each optimized and wild type)

hnmt-pcr-substr1.png

We added 6X DNA Loading dye to each PCR tubes. We loaded the wells of the gels with 12μL of DNA solution in the following order: 

hnmt-pcr.png 1. S1O (optimized) 2. S1W (wild type) 3. N1O (optimized) 4. N1W (wild type) 5. Ladder


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]