User:Linh N Le/Notebook/2009/08/12: Difference between revisions

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*Andy has done initial testing to show that the kinesin we have and the MT's are still in good order
*Andy has done initial testing to show that the kinesin we have and the MT's are still in good order
*The idea now is that the lipids are too concentrated (and the layers are too thick) so we will dilute them down
*The idea now is that the lipids are too concentrated (and the layers are too thick) so we will dilute them down
**Andy diluted the lipids from 10mg/ml to 1mg/ml using chloroform
*Andy spun-coated a cover glass with 1/2 lipids 1/2 naked
*Added kinesin + brb solution to the lipids and letting it sit
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Revision as of 11:45, 12 August 2009

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To Do

  • Motility assay (w/lipids)

Shaker

  • Koch was unsure about the "temperature gradient" i had reported on yesterday, and I may have made a mistake when starting as such
    • What happened is I got two statements mixed up
  • To quote the manual:
    • "Depending on various conditions within the chamber, such as flask placement and size, the heat produced by growing organisms, heat losses due to liquid evaporation from flasks, etc., the display temperature may differ from the temperatures within the flasks themselves"
    • "The temperature probe measures the temperature of the air at the probe's location, near the heat exchanger return vent."

Motility

  • Andy wants to try to mix up a new batch of kinesin and retry his lipids assay
    • Oops, he's using the old stuff
  • He also wants to redo a "standard" motility assay to make sure everything is working
  • Andy has done initial testing to show that the kinesin we have and the MT's are still in good order
  • The idea now is that the lipids are too concentrated (and the layers are too thick) so we will dilute them down
    • Andy diluted the lipids from 10mg/ml to 1mg/ml using chloroform
  • Andy spun-coated a cover glass with 1/2 lipids 1/2 naked
  • Added kinesin + brb solution to the lipids and letting it sit
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