Team:UNICAMP-Brazil/Notebooks/October 19

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(New page: {{:Team:UNICAMP-Brazil/inc_topo}} {{:Team:UNICAMP-Brazil/inc calendar}} __NOTOC__ ==''' YeastGuard '''== ====New strategy: pGEM==== *<p style=”text-align:justify;”>We sent the pDL...)
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*<p style=”text-align:justify;”>We did PCR with 30 yeast colonies transformed with Adh1+Lysozyme and pDLD+Lysozyme. Unfortunately none of the colonies had the correct vector =/</p>
*<p style=”text-align:justify;”>We did PCR with 30 yeast colonies transformed with Adh1+Lysozyme and pDLD+Lysozyme. Unfortunately none of the colonies had the correct vector =/</p>
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[[Image:adh1+lis2.jpg|300px|center]]
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[[Image:pDLD+lis.jpg|500px|center]]
*<p style=”text-align:justify;”>We have no time to repeat the transformations =( Our hope is that there has been a problem to the PCR reaction and that the parts are correctly connected to the YEP vector. So we decided to go on with the transformed yeasts we have.</p>
*<p style=”text-align:justify;”>We have no time to repeat the transformations =( Our hope is that there has been a problem to the PCR reaction and that the parts are correctly connected to the YEP vector. So we decided to go on with the transformed yeasts we have.</p>

Revision as of 05:42, 21 October 2009

Topo l2.gif topo_r_igem.gif
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YeastGuard

New strategy: pGEM

  • We sent the pDLD+lysozyme device to iGEM today. =)

Yeast experiments

  • There are plenty of yeast colonies in the pDLD+Lys and Adh1+Lys plates. =)

  • We did PCR with 30 yeast colonies transformed with Adh1+Lysozyme and pDLD+Lysozyme. Unfortunately none of the colonies had the correct vector =/

Adh1+lis2.jpg
PDLD+lis.jpg
  • We have no time to repeat the transformations =( Our hope is that there has been a problem to the PCR reaction and that the parts are correctly connected to the YEP vector. So we decided to go on with the transformed yeasts we have.

  • At night we find plenty yeast colonies in the pDLD+YFP and Adh1+YFP plates.

  • Considering our lack of time we decided to collect a pool of yeast colonies for each construction and inoculate in liquid media. This strategy was adopted for both constructions (pDLD+YFP and Adh1+YFP). These pre inocula will be used for induction tests of Lysozyme tomorrow.


Raíssa and Taís