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Team:Caltech/Week 7 - 2010.igem.org
 

Team:Caltech/Week 7

From 2010.igem.org

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(added Mon info)
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==Monday 7/26==
==Monday 7/26==
 +
* Started PCR reaction to extract the HSP (K112400) from its Berkeley Standard backbone (BBb). (Used same PCR parameters as CPCR from 7/22.
 +
* Group meeting!
 +
** By next week: Need to design test-construct experiments, as they will be ready sometime early next week.
 +
*** Can use PCR machine to achieve easy temperature gradients
 +
*** Use spectrophotometer and eventually microscope to assay fluorescence.
 +
*** Consider a plate assay?
 +
** AIBN issues:
 +
*** Consider using low-concentration DMSO to help dissolve AIBN in LB/cell mixture.
 +
*** Need to figure out how much unreacted (or otherwise) AIBN remains after mixing with cells.
 +
*** Need to test crosslinking using hydrolyzed and epoxidized oil mixed with lysate and with cells to tweak concentration of AIBN needed, and to see what it makes.
 +
** TGase:
 +
*** purchase urea?
 +
*** To prevent a solid plug forming upon addition of TGase powder to sample, prepare liquid stock of concentrated TGase.
 +
** Wiki:
 +
*** Should visit biofab.org for research material for human impact segment.
 +
** In general, we should set goals for both the end of SURF and for the end of the summer and determine what we need to do to get on track for them.
 +
*** Printing in 2D
 +
*** Working AND gate, at least in bulk fluid
 +
*** Characterization of 3D hydrogel/plastic
 +
*** Crosslinking data
 +
* PCR purified K112400 PCR product & digested as plasmid insert.
 +
* Transformed RFP bricks of verious resistances to use as backbone for future ligations
 +
* Ran 2 gels of today's CPCR products:
==Tuesday 7/27==
==Tuesday 7/27==
 +
*
==Wednesday 7/28==
==Wednesday 7/28==

Revision as of 04:56, 28 July 2010


iGEM 2010



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Monday 7/26

  • Started PCR reaction to extract the HSP (K112400) from its Berkeley Standard backbone (BBb). (Used same PCR parameters as CPCR from 7/22.
  • Group meeting!
    • By next week: Need to design test-construct experiments, as they will be ready sometime early next week.
      • Can use PCR machine to achieve easy temperature gradients
      • Use spectrophotometer and eventually microscope to assay fluorescence.
      • Consider a plate assay?
    • AIBN issues:
      • Consider using low-concentration DMSO to help dissolve AIBN in LB/cell mixture.
      • Need to figure out how much unreacted (or otherwise) AIBN remains after mixing with cells.
      • Need to test crosslinking using hydrolyzed and epoxidized oil mixed with lysate and with cells to tweak concentration of AIBN needed, and to see what it makes.
    • TGase:
      • purchase urea?
      • To prevent a solid plug forming upon addition of TGase powder to sample, prepare liquid stock of concentrated TGase.
    • Wiki:
      • Should visit biofab.org for research material for human impact segment.
    • In general, we should set goals for both the end of SURF and for the end of the summer and determine what we need to do to get on track for them.
      • Printing in 2D
      • Working AND gate, at least in bulk fluid
      • Characterization of 3D hydrogel/plastic
      • Crosslinking data
  • PCR purified K112400 PCR product & digested as plasmid insert.
  • Transformed RFP bricks of verious resistances to use as backbone for future ligations
  • Ran 2 gels of today's CPCR products:

Tuesday 7/27

Wednesday 7/28

Thursday 7/29

Friday 7/30

Weekend 7/31-8/1

 
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