Team:Goettingen/week10-3

From 2012.igem.org

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TARY149F150T154Fw: <br>gcgcaGGAAAGGTCTCAGGAGCTnnNnnNGCTCAGCCAnnNCAGGGAATGCAAAATGCAATGGGCGAAG<br>
TARY149F150T154Fw: <br>gcgcaGGAAAGGTCTCAGGAGCTnnNnnNGCTCAGCCAnnNCAGGGAATGCAAAATGCAATGGGCGAAG<br>
TARY149F150T154Rv: <br>gcgcaGAGTAGGTCTCACTCCAGTATTGCCATAATCTAGGTAATC<br><br>
TARY149F150T154Rv: <br>gcgcaGAGTAGGTCTCACTCCAGTATTGCCATAATCTAGGTAATC<br><br>
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We firstly did a test PCR with both primer pairs to verify the <a href="https://2012.igem.org/Team:Goettingen/Project/Methods">mutagenesis PCR protocol</a> and conditions.  
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We firstly did a test PCR with both primer pairs to verify the <a href="https://2012.igem.org/Team:Goettingen/Project/Methods">mutagenesis PCR protocol</a> and conditions. As a template we use pSB1C3_TAR_QC_18C since this promoter is the strongest among the promoter constructs we use.
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<li>Observations and results: <br>According to the agarose gel the PCR worked well. A band at the expected size of 3769 bp was observed for both reactions.
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Revision as of 09:28, 20 September 2012