Team:Paris Liliane Bettencourt/Notebook/2010/07/06/

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</li><li>10 µL of ladder 1Kb
</li><li>10 µL of ladder 1Kb
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<p style="display:block;">Migration&nbsp;: 50V, 1h30  
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<p style="display:block;">Migration&nbsp;: 50V, 1h30<br />
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The bands of the ladder are not well separated. Thus, the migration should last longer and the gel should be at 1,0% agarose.
</p><p style="display:block;">https://static.igem.org/mediawiki/2010/9/99/Electrophoresis_060710.jpg
</p><p style="display:block;">https://static.igem.org/mediawiki/2010/9/99/Electrophoresis_060710.jpg
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<br />The bands of the ladder are not well separated. Thus, the migration should last longer and the gel should be at 1,0% agarose.
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Latest revision as of 19:26, 26 October 2010



Raphaël, Théotime and Stéphane

Miniprep - Kit Qiagen - Final volume : 50µL (Raphaël)

  • pSUlib - attC KanR

Miniprep - Kit Promega (Stéphane)

  • pSUlib - attC KanR

Restriction digest - Xba I

  • pSUlib - attC KanR (Qiagen and Promega Minipreps)

Final volume : 20 µL
15 µL distilled water
2 µL minipreped DNA
0,2 µL BSA 100x
2 µL buffer 10x
1 µL restriction enzyme

Protocol


1- Add in order listed above.
2- Vortex the mix 2 sec, spindown in micro-centrifuge and put in 37°C for 2h.

DNA Gel electrophoresis (agarose 1,5% w/v)


7,5g of agarose in 500mL of TBE buffer 0,5x
2 µL of EtBr was added in the gel

Protocol (2 wells)

  • 10 µL of minipreped DNA (Qiagen) + 2 µL of loading buffer 6x
  • 10 µL of ladder 1Kb

Migration : 50V, 1h30

DNA Gel electrophoresis (agarose 1,0% w/v)


2 µL of EtBr was added in the gel

Protocol (2 wells)

  • 10 µL of minipreped DNA (Promega) + 2 µL of loading buffer 6x
  • 10 µL of ladder 1Kb

Migration : 50V, 1h30
The bands of the ladder are not well separated. Thus, the migration should last longer and the gel should be at 1,0% agarose.

Electrophoresis_060710.jpg