User:Daniel Ramirez/Notebook/UNAM Genomics Mexico 2011/2011/09/03

From OpenWetWare
Jump to navigationJump to search
UNAM Genomics Mexico 2011 <html><img src="/images/9/94/Report.png" border="0" /></html> Main project page
<html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>Previous entry<html>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</html>Next entry<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>

χρόνος πέρασμα September 3rd 2011

HydA CAI Optimizacion Control

ABSTRACT
  • The double digestions of the bioparts B0015 and J04500 were succesful. Gel extraction of these double digestions.

  • Today I ran a 1% agarose electrophoretic gel to see if the double digestions of the bioparts J04500 and B0015 were made correctly. 130 V 35 minutes.


  • Lane #1 contains a 250 bp Ladder; lanes #2 and #3 contain the non-digested plasmids carrying B0015 and J04500, respectively; lanes #4 and #5 contain the double digested plasmids carrying B0015 and J04500, respectively. They were well digested.



  • As these double digestions cut and left a tiny fragment of dna that in theory could be religated to its original plasmid if the solution put to ligate, I tried to avoid this annoyance using QIAEX II Gel Extraction Kit to extract only the desired digested fragment from each digestion. Once extracted, I ran a 1% agarose electrophoretic gel to see if the extraction was succesful. 130 V 35 minutes.



  • Although barely, two bands of approximately the expected sizes can be observed. Maybe concentrating the solution might improve the probabilities of a succesful ligation.