User:Linh N Le/Notebook/2009/08/13: Difference between revisions
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*There may have been a chance that the lipids worked, but when you can only see a MT for ~3s, theres not really a good way to confirm it | *There may have been a chance that the lipids worked, but when you can only see a MT for ~3s, theres not really a good way to confirm it | ||
==Hancock Paper== | |||
* I read the Hancock paper that Andy sent me about surface passivization | |||
*There are 2 questions that I had for Andy about that paper: | |||
*#The paper states that k-casein is the worst for kinesin binding and kinesin-MT binding (the only "upside" is that only long MT's stick) | |||
** [[User:Andy Maloney|Andy Maloney]] 15:54, 14 August 2009 (EDT): Yes. Was there something more you needed clarifying? I don't understand if you have a question. | |||
*#When they prepare BRB80 w/casein, they stated the centrifuged out the non-dissolved particles whereas we wanted it to completely go into solution yesterday | |||
** [[User:Andy Maloney|Andy Maloney]] 15:54, 14 August 2009 (EDT): Again, yes. You make a valid point. What is your specific question? As Koch mentioned, these are good points from the paper but I don't know if you are asking me a question or not. | |||
** [[User:Steven J. Koch|Steve Koch]]:Wow, these are both really good points. In regards to the first, didn't the motility work really well for you with the kappa casein the other day? | |||
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Motility
Hancock Paper
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