Team:UNICAMP-Brazil/Notebooks/September 7

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* Now that we have purified samples of the finO and finP sequences (see September 6th for more details), and once we could also recover the pSB1A3 vector (August 10th), it's time to start the construction of our novel biobricks, which will be responsible for inhibiting the conjugation process in our labor cells model (see project overview for further information).
* Now that we have purified samples of the finO and finP sequences (see September 6th for more details), and once we could also recover the pSB1A3 vector (August 10th), it's time to start the construction of our novel biobricks, which will be responsible for inhibiting the conjugation process in our labor cells model (see project overview for further information).
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* In order to achieve this objective, we permorfed today the digestion (according to protocol X, see Protocols Section) of the purified sequences finO and finP, and also of the vector pSB1A3. We digested for 3 hours.
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* In order to achieve this objective, we permorfed today the digestion (according to protocol X, see Protocols Section) of the purified sequences finO and finP, and also of the vector pSB1A3. The digestion lasted 3 hours.
* After that, we run an agarose gel of the digested product aiming the confirmation of the assay. According to the gel, the vector pSB1A3 was succesful digested. As for the sequences finO and finP, both of them appeared in the gel, but it's not possible to assure that they indeed were digested since the gel resolution does not differentiate just a few base pairs (excised by digestion). Therefore, we need to ligate those sequences in the digested vector in order to confirm that they both were also digested.  
* After that, we run an agarose gel of the digested product aiming the confirmation of the assay. According to the gel, the vector pSB1A3 was succesful digested. As for the sequences finO and finP, both of them appeared in the gel, but it's not possible to assure that they indeed were digested since the gel resolution does not differentiate just a few base pairs (excised by digestion). Therefore, we need to ligate those sequences in the digested vector in order to confirm that they both were also digested.  

Revision as of 14:40, 14 September 2009

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YeastGuard

WIKI

Today we worked on updating the wiki!

Lactate Permease (JEN1 ORF)

Considering that we didn´t have a specific band in the digestion from the JEN1, we decided to repeat the PCR (we think it was not totally specific) and to purify the correct band. So today we repeated the PCR for the JEN1 ORF.

ColiGuard

finO, finP and pSB1A3 digestion

  • Now that we have purified samples of the finO and finP sequences (see September 6th for more details), and once we could also recover the pSB1A3 vector (August 10th), it's time to start the construction of our novel biobricks, which will be responsible for inhibiting the conjugation process in our labor cells model (see project overview for further information).
  • In order to achieve this objective, we permorfed today the digestion (according to protocol X, see Protocols Section) of the purified sequences finO and finP, and also of the vector pSB1A3. The digestion lasted 3 hours.
  • After that, we run an agarose gel of the digested product aiming the confirmation of the assay. According to the gel, the vector pSB1A3 was succesful digested. As for the sequences finO and finP, both of them appeared in the gel, but it's not possible to assure that they indeed were digested since the gel resolution does not differentiate just a few base pairs (excised by digestion). Therefore, we need to ligate those sequences in the digested vector in order to confirm that they both were also digested.

Marcelo





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