Team:IPN-UNAM-Mexico/Notebook/August 7 2009

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                                   <td><p>&nbsp;</p>
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                                   <td><p align="right">&nbsp;</p>
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                                     <p align="left" class="style8"><strong>August 7th, 2009</strong></p>
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                                     <p align="right"><img src="https://static.igem.org/mediawiki/2009/a/a6/LabIconMX.png" alt="LabNotebook" width="30" height="35"> <span><a href="https://2009.igem.org/Team:IPN-UNAM-Mexico/Notebook">Back to Notebook</a></span></p>
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                                    <p><strong>August 7th, 2009</strong></p>
                                     <p align="left" class="style8"><br>
                                     <p align="left" class="style8"><br>
                                       Digestion Digestion using EcoRI : </p>
                                       Digestion Digestion using EcoRI : </p>

Latest revision as of 08:15, 14 October 2009



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August 7th, 2009


Digestion Digestion using EcoRI :

  • plasmidicDNA..........3μl
  • Buffer 2....................1μl     x30
  • BSA..........................0.5μl  x30
  • EcoRI enzyme......... 0.5μl   x30
  • H2O..........................5μl
 

An electrophoresis gel was ran with the following quantities:

  • 3μl marker 1kb
  • Buffer 2 ................ 1μl.
  • 3μl DNA+ 3μl of colorant

All samples were digested with EcoRI in order to linearized them.

Line 1 1kb | 3.1 ....* 3.4|9.1....* 9.9|9.8.. 1|1kb|*18.2....18.4|19.1*....19.4|1kb

line  2 1kb|22.1.......*22.4|24.2”   16.2” 14.1 9.4|1kb

the ones marked with * are plasmids extracted today.

 

 

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