IGEM:Harvard/2006/DNA nanostructures/Notebook/2006-8-8: Difference between revisions

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*c6.0B (in aptamers)
*c6.0B (in aptamers)
*c6.0C (out aptamers)
*c6.0C (out aptamers)
====Protocol====
Each reaction:
*9 {{ul}} p7308 scaffold (44 nM)
*16 {{ul}} oligo stock (250 nM)
*4 {{ul}} 10x folding buffer (500 mM HEPES pH 7.5, 500 mM NaCl, 100 mM {{mgcl2}})
*11 {{ul}} d{{h2o}}
Folding conditions:
*start at 80{{c}}, decrement 1{{c}} every 2 min. for 60 cycles.
====Gel Analysis====
*Run 2% agarose gel, supplemented to 10 mM {{mgcl2}}
*Run in 1x TBE supplemented to 10 mM {{mgcl2}}

Revision as of 12:14, 8 August 2006

Folding Rxns w/ New Ligands

Design 3

  • c3.2F (latch 1, in aptamers)
  • c3.2G (latch 1, out aptamers)
  • c3.2H (latch 2, in aptamers)
  • c3.2I (latch 2, out aptamers)

Design 4

  • c4.0F (latch 1, in atpamers)
  • c4.0G (latch 1, out aptamers)
  • c4.0H (latch 2, in aptamers)
  • c4.0I (latch 2, out aptamers)

Design 5

  • c5.0C (latch 2, in aptamers)
  • c5.0D (latch 2, out aptamers)

Design 6

  • c6.0A (no aptamers)
  • c6.0B (in aptamers)
  • c6.0C (out aptamers)

Protocol

Each reaction:

  • 9 μL p7308 scaffold (44 nM)
  • 16 μL oligo stock (250 nM)
  • 4 μL 10x folding buffer (500 mM HEPES pH 7.5, 500 mM NaCl, 100 mM MgCl2)
  • 11 μL dH2O

Folding conditions:

  • start at 80[[:Category:{{{1}}}|{{{1}}}]], decrement 1[[:Category:{{{1}}}|{{{1}}}]] every 2 min. for 60 cycles.

Gel Analysis

  • Run 2% agarose gel, supplemented to 10 mM MgCl2
  • Run in 1x TBE supplemented to 10 mM MgCl2