Difference between revisions of "Part:BBa K5492020"

 
 
(3 intermediate revisions by 2 users not shown)
Line 4: Line 4:
  
 
Forward primer sequence of the adapter sequence utilised by GenScript.
 
Forward primer sequence of the adapter sequence utilised by GenScript.
 +
Utilised in PCR reactions for part [https://parts.igem.org/Part:BBa_K5492402 BBa_K5492402] and [https://parts.igem.org/Part:BBa_K5492403 BBa_K5492403].
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here
Line 9: Line 10:
  
 
<!-- -->
 
<!-- -->
<span class='h3bb'>Sequence and Features</span>
+
===Experiments===
<partinfo>BBa_K5492020 SequenceAndFeatures</partinfo>
+
==PCR – HNMT==
 +
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>
  
 
<!-- Uncomment this to enable Functional Parameter display  
 
<!-- Uncomment this to enable Functional Parameter display  

Latest revision as of 11:38, 2 October 2024


Genscript adapter forward primer

Forward 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]