User:Steven J. Koch/Notebook/Kochlab/2009/06/16/Motility assays

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Steve Koch 16:52, 16 June 2009 (EDT): We're going to give motility assays a try.

Linh's notes: http://openwetware.org/wiki/User:Linh_N_Le/Notebook/2009/06/16#kinesin

Contents

Attempt at assay

  • Made a double flow chamber. Top will be just motility solution. Bottom will be full motility assay.
  • Incubating with BRB80CS0.5 for 5 minutes (just over) (sample volume is about 14 ul)
  • Incubating with kinesin (diluted 1:10 in BRB80CA), 15 ul, just over 5 minutes.
  • Flowed in 15 ul motility solution. Observing now.

Kinesin

We're going to try an old aliquot of drosophila kinesin that I have from 2004. Yeah, that's really old, but hopefully it will have a little activity. I don't have a lot of details about the kinesin. So, we're just going to assume that the stock I have is 20 ul of about 1 mg / ml protein. I think for the first attempt, we should dilute this 5 microliters plus 45 ul of BRB80CA.

  • Brigette is adding 45 ul of BRB80CA to a new tube
  • Then adding 5 ul of "1 mg / ml" kinesin

BRB80CT

Brigette made more BRB80T, using PEM from cytoskeleton. She actually made it with 20 μM taxol (as opposed to the usual 10 micromolar)--this is fine.

Brigette made BRB80CT by adding 50 μL of 2 mg/ ml casein to 450 μL of BRB80T.

BRB80CA

Steve Koch 19:00, 16 June 2009 (EDT): I was a little worried that theATP wasn't mixed properly. We should keep this in mind.

MTs

Brigette polymerized one of the 1 ul aliquots of TRITC tubulin from yesterday. Stabilized with (approx 50 ul) of BRB80T. Then after making more BRB80T, she added to bring up to approximately 100 ul. Linh verified that we had tubes via microscopy w/o antifade.

Antifade

Linh is checking whether the aliquot of antifade from yesterday is OK.

Things to order

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