Team:UFAM Brazil/7-9-2014

From 2014.igem.org

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<p>  Today we decided to work on the transformation once again with <i>Escherichia coli</i> DH5α RR1 using Transformation Efficiency Kit as a control and the DNA diluted from the DNAa Parts Kit 2013 (BBa_E0840), using iGEM’s standard transformation protocol. We have to be very careful!!!!</p>
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<p>  Today we decided to work on the transformation once again with <i>Escherichia coli</i> DH5α RR1 using Transformation Efficiency Kit as a control and DNA diluted from DNAa Parts Kit 2013 (BBa_E0840), using iGEM’s standard transformation protocol. We have to be very careful!!!!</p>
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<p> We had a big meeting with all our team members.</p>
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<p> We also had a big meeting with all our team members.</p>
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Latest revision as of 23:18, 16 October 2014

07/09/2014

The transformation with pUC72 using approximately 1.000 ng/ul and 1 ng/ul worked!! But our transformation with the DNA diluted from the Kit Parts 2013 (BBa_E0840) didn’t grow any transforming cells!!! =(

Today we decided to work on the transformation once again with Escherichia coli DH5α RR1 using Transformation Efficiency Kit as a control and DNA diluted from DNAa Parts Kit 2013 (BBa_E0840), using iGEM’s standard transformation protocol. We have to be very careful!!!!

We also had a big meeting with all our team members.

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