Team:Paris/August 6

From 2008.igem.org

(Difference between revisions)
(Digestion)
(Analysis of yesterday's gel extraction (assay to quantify the DNA contained in the eluate))
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===Analysis of yesterday's gel extraction (assay to quantify the DNA contained in the eluate)===
===Analysis of yesterday's gel extraction (assay to quantify the DNA contained in the eluate)===
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The samples analysed are the minipreps eluate of MP123 and the Gel Extraction eluate of the PCR products from MP124, MP125, MP126 and MP127.
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In order to quantify the DNA contained either in the Miniprep product of MP123 or in the PCR products of MP124, MP125, MP126 and MP127 previously purifed by QIAquick Gel Extraction, we carry out an elctrophoresis assay in a 1,5% agarose gel. The ladder used was the 100 bp DNA ladder (New England Biolabs). We added 1 µL of 6X blue loading dye on 5 µL of each sample, which were then loaded on the gel.

Revision as of 12:12, 6 August 2008

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Plasmid extraction

Digestion

For each sample (MP123 and PCR products of MP124, MP125, MP126 and MP127 previously purified by QIAquick Gel Extraction):

  • 10 µL of DNA (Miniprep eluate or Gel extraction eluate of the PCR products)
  • 12,5 µL water
  • 2,5 µL buffer 2
  • 0,25 µL BSA
  • 1 µL EcoRI

The reaction was incubated 1h30 at 37°C, then 1h30 more after adding 1 µL of SpeI.

Analysis of yesterday's gel extraction (assay to quantify the DNA contained in the eluate)

In order to quantify the DNA contained either in the Miniprep product of MP123 or in the PCR products of MP124, MP125, MP126 and MP127 previously purifed by QIAquick Gel Extraction, we carry out an elctrophoresis assay in a 1,5% agarose gel. The ladder used was the 100 bp DNA ladder (New England Biolabs). We added 1 µL of 6X blue loading dye on 5 µL of each sample, which were then loaded on the gel.