Notes 20110623

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  • Attendees: David Rostcheck, Philip Wrage, Jonathan Shook, John Haskins, Joe Southwell
  • Makerspace space committee is likely going to swap us into a portion of classroom 2/electronics bay because bio interest is growing and it's bigger
  • John took the MIT 7.012 intro biology lectures online. He noted that 7.012 lectures punt on cell differentiation and wanted to learn more about it
  • Could we do actual research? Some is feasible - for example, sequencing samples of water or air to discover new organisms. See [Craig Venter's exploratory boat expedition] to sample the oceans
  • Discussion of animal models - stick to simple organisms (bacteria, yeast, plants, maybe flies)
  • Philip has bought some equipment:
    • two thermocyclers
    • two vortexes
    • three gel electrophoresis rig
    • two power supplies (one working, one needs repair)
    • over 100 flasks
    • 100 expired but maybe still useful DNA purification kits
    • one micro-centrifuge (no speed control - adding speed reduction control might be cool project)
    • a shaking, heated water bath (condition unknown)
    • binocular oil immersion microscope
    • UV illuminating box
    • Stackable bioreactors
    • Micropipette tips (various sizes; won't do any good until we have micropipetters)
  • We still need:
  • The seller he bought them from has more centrifuges and maybe more useful stuff
  • We should put up a wish list of things we want, so members can buy and donate them
  • We can build an incubator, or buy cheap on eBay
  • A pressure cooker is a sufficient alternative to an autoclave. See if we can find one on Craigslist.
  • Still looking for -80 C freezers. Philip's seller has stainless racks for them.
  • Philip explained the theory of how to clone a gene
  • Can we build out own sequencer? Yes, maybe, although we can also buy them for a few thousand on eBay (unknown whether software is included)
  • David R talked to Raymond McCauley from BioCurious about lessons learned. Most of them were not so applicable to us: they had real issues negotiating the regulatory bureaucracy around zoning and safety that appear to be more specific to California. Being embedded in the Makerspace also helps us
  • Andrew Hessel suggests talking to GenSpace in NYC; they have a very effective model.
  • The book "BioPunk" came out and is arousing interest in synthetic biology
  • There was a recent USA Today article on BioCurious
  • Next steps: design trays and combs for gel electrophoresis rig
  • We talked through running a PCR lab. We have the equipment (need consumable reagents). To show that the PCR worked, we need to do a gel electrophoresis. However, the ethidium bromide used to bind to the DNA and fluoresce (to show where it ends up) is a seriously dangerous chemical (teratogenic and mutagenic), requires safe handling, locked storage, hazardous waste disposal
  • See this article on gel electrophoresis
  • And this one on alternatives to ethidium bromide