User:Pranav Rathi/Notebook/OT/2011/01/10/DNA tethering experiments: Difference between revisions

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(New page: I attempt tethering again today with new beads and new anti-dig. ===Ant-dig=== Dr. Koch and I prepared new anti-dig: 1X concentration *PBS [http://en.wikipedia.org/wiki/Phosphate_buffered...)
 
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# Flow BGB 50μl + seal it with nail polish
# Flow BGB 50μl + seal it with nail polish
===Results===
===Results===
[http://www.evernote.com/pub/pranavrathi1/dnastretching]
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Revision as of 21:51, 10 January 2011

I attempt tethering again today with new beads and new anti-dig.

Ant-dig

Dr. Koch and I prepared new anti-dig: 1X concentration

  • PBS [1]180μl + aliquots 20μl = [MIX] = Anti-dig 200μl.

PBS was used from the glass door fridge and aliquot from super cold gray fridge. I used two different beads:

  • 1 μm new beads (looks good in microscope), 20μl from the batch. 5μl (batch) +4 5μl BGB = 50μl.
  • .5μm (FL) expired on 01/07/2010.5μl (batch)+45μl BGB = 50μl.

Procedure[2]

  1. Flow anti-dig 10μl wait for 5 min.
  2. Flow BGB 50μl wait for 2 min.
  3. Flow 1.1kb (new)10μl wait for 14 min.
  4. Flow BGB wait none.
  5. Flow micro-spheres one in each chamber 10μl wait for 14 min.
  6. Flow BGB 50μl + seal it with nail polish

Results

[3]

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