Haynes Lab:Notebook/Investigating Photo-Switchable Synthetic Nucleosomes/2012/11/12

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| LOV || 0.048 || 0.026 || 1.860 || 48.095
| LOV || 0.048 || 0.026 || 1.860 || 48.095
|}
|}
 +
 +
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----
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Great! Next step...
 +
 +
* Digests:
 +
** In a 30 μL reaction, cut H2B with XbaI and SpeI
 +
** In a 30 μL reaction, cut LOV with XbaI and SpeI
 +
** In a 30 μL reaction, cut a pSB1A2 plasmid (from Rene) XbaI and SpeI
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 +
{| class="wikitable" border=1 cellpadding="5" cellspacing="0"
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|-
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| Reagent || H2B|| LOV || pSB1A2
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|-
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| DNA || 8.0 || 8.0 || 15.0
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|-
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| XbaI || 1.0|| 1.0 || 1.0
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|-
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| SpeI || 1.0 || 1.0 || 1.0
 +
|-
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| 10x buffer || 3.0 || 3.0 || 3.0
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|-
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| dH<sub>2</sub>O || --- || --- || ---
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|-
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| Total vol. || 30. 0 || 30.0  || 30.0
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|}
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 +
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* Run entire 30 μL on a 1% gel (use the big fat-tooth well comb)
 +
* Cut band out of gel (use UV box); H2B = ~410, LOV = ~461, pSB1A2 = ~2000
 +
* Extract DNA from gel

Revision as of 19:25, 13 November 2012

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November 12, 2012

  • The PCR products were purified with the Zymo DNA Clean and Concentration Kit
PCR Product 260 280 260/280 ng/μL
H2B 0.052 0.028 1.865 51.607
LOV 0.048 0.026 1.860 48.095


Great! Next step...

  • Digests:
    • In a 30 μL reaction, cut H2B with XbaI and SpeI
    • In a 30 μL reaction, cut LOV with XbaI and SpeI
    • In a 30 μL reaction, cut a pSB1A2 plasmid (from Rene) XbaI and SpeI
Reagent H2B LOV pSB1A2
DNA 8.0 8.0 15.0
XbaI 1.0 1.0 1.0
SpeI 1.0 1.0 1.0
10x buffer 3.0 3.0 3.0
dH2O --- --- ---
Total vol. 30. 0 30.0 30.0


  • Run entire 30 μL on a 1% gel (use the big fat-tooth well comb)
  • Cut band out of gel (use UV box); H2B = ~410, LOV = ~461, pSB1A2 = ~2000
  • Extract DNA from gel



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