Team:UFAM Brazil/7-16-2014

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<table class="mainTable">
<table class="mainTable">
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<tr><td><h1>07/11/2014</h1></td></tr>
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<tr><td><h1>07/16/2014</h1></td></tr>
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<tr><td colspan="3" align="justify"> <p>Today we had a meeting with the Secretary of Sustainable Development from Amazon.  So freaking cooll!!  
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<tr><td colspan="3" align="justify"> <p>Today we had a meeting with the Secretary of Sustainable Development of Amazon.  So freaking cooll!!  
</p>
</p>
<p>We also had a magna meeting!!! With all of our team members.</p>
<p>We also had a magna meeting!!! With all of our team members.</p>
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<p>Transformation has finally worked !!!!!! Our biobricks were finally cloned into the bacteria!</p>
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<p>Transformation has finally worked!!!!!! Our biobricks were finally cloned into the bacteria!</p>
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<tr><td  colspan="3" align="center"><p><b>- DH5α com BBa_E0840 – pSB1C3 (Biodetection Biobrick);</b></p>
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<tr><td  colspan="3" align="center"><p><b>- DH5α with BBa_E0840 – pSB1C3 (Biodetection Biobrick);</b></p>
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<tr><td  colspan="3" align="center"><p><b>- DH5α com BBa_K346004 – pSB1C3 (Bioaccumulation biobrick).</b></p>
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<tr><td  colspan="3" align="center"><p><b>- DH5α with BBa_K346004 – pSB1C3 (Bioaccumulation biobrick).</b></p>
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<tr><td  colspan="3" align="justify"><p style="margin-top:20px">Today we are going to inoculate the transformation in liquid LB media chloranphenicol 34ug/ml for miniprep purposes. We’re also going to inoculate JM110 with streptomycin 40ug/ml.</p>
<tr><td  colspan="3" align="justify"><p style="margin-top:20px">Today we are going to inoculate the transformation in liquid LB media chloranphenicol 34ug/ml for miniprep purposes. We’re also going to inoculate JM110 with streptomycin 40ug/ml.</p>
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<p> For the genetic constructions we are going to use the Xbal enzyme in order to do this we need a DNA without mutilation dam .We cloned the bacteria into the (DH5α) dam positive, but we’re still going to transform the multiplied and concentrated plasmid into JM110, so that it loses its methylation in the Xbal restriction sites.</p>
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<p> For the genetic constructions we are going to use the Xbal enzyme. To achieve this we need DNA without methylation dam. We cloned the bacteria into the (DH5α) dam positive, but we’re still going to transform the multiplied and concentrated plasmid into JM110, so that it will lose its methylation in the Xbal restriction sites.</p>

Latest revision as of 23:50, 16 October 2014

07/16/2014

Today we had a meeting with the Secretary of Sustainable Development of Amazon. So freaking cooll!!

We also had a magna meeting!!! With all of our team members.

Transformation has finally worked!!!!!! Our biobricks were finally cloned into the bacteria!

- DH5α with BBa_E0840 – pSB1C3 (Biodetection Biobrick);

- DH5α with BBa_K346004 – pSB1C3 (Bioaccumulation biobrick).

- DH5α with positive control pUC72

Today we are going to inoculate the transformation in liquid LB media chloranphenicol 34ug/ml for miniprep purposes. We’re also going to inoculate JM110 with streptomycin 40ug/ml.

For the genetic constructions we are going to use the Xbal enzyme. To achieve this we need DNA without methylation dam. We cloned the bacteria into the (DH5α) dam positive, but we’re still going to transform the multiplied and concentrated plasmid into JM110, so that it will lose its methylation in the Xbal restriction sites.

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