Team:University of Lethbridge/Notebook/GeneralLabJuly

From 2008.igem.org

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====Nathan Puhl, Andrew====
====Nathan Puhl, Andrew====
Made 500 mL of LB agar + amp and 500 mL of Liquid LB
Made 500 mL of LB agar + amp and 500 mL of Liquid LB
 +
===July 2, 2008===
===July 2, 2008===
====Nathan Puhl, Alix, Sebastian, Munima, Roxanne, Christa====
====Nathan Puhl, Alix, Sebastian, Munima, Roxanne, Christa====
-
Trasformed BBa_J24679( RBS + LacI), BBa_P0440 (RBS+TetR+T10+T12), leftover DNA from Double T (June 26, 2008), and 1 uL of pSB1A7 plasmid (June 18).
+
Transformed BBa_J24679 (RBS + LacI), BBa_P0440 (RBS+TetR+T10+T12), leftover DNA from Double T (June 26, 2008), and 1 uL of pSB1A7 plasmid (June 18, 2008).
Protocol changes:   
Protocol changes:   
   -3 uL of DNA
   -3 uL of DNA
   -spin down 200 uL of cells and resuspend in 100 uL of LB; plate on LB + amp
   -spin down 200 uL of cells and resuspend in 100 uL of LB; plate on LB + amp
 +
===July 3, 2008===
===July 3, 2008===
====Nathan Puhl, Munima, Christa, Alix, Roxanne, Sebastian====
====Nathan Puhl, Munima, Christa, Alix, Roxanne, Sebastian====
Checked transformation plates.  Only the positive control (pSB1A7) had colonies (~1500) indicating that there is nothing wrong with the transformation protocol or cells so we must be having problems with the DNA extraction from the filter paper.  Next week we will attempt various changes to the protocol to extract more DNA.
Checked transformation plates.  Only the positive control (pSB1A7) had colonies (~1500) indicating that there is nothing wrong with the transformation protocol or cells so we must be having problems with the DNA extraction from the filter paper.  Next week we will attempt various changes to the protocol to extract more DNA.

Revision as of 16:20, 4 July 2008

Contents

July 1, 2008

Nathan Puhl, Andrew

Made 500 mL of LB agar + amp and 500 mL of Liquid LB


July 2, 2008

Nathan Puhl, Alix, Sebastian, Munima, Roxanne, Christa

Transformed BBa_J24679 (RBS + LacI), BBa_P0440 (RBS+TetR+T10+T12), leftover DNA from Double T (June 26, 2008), and 1 uL of pSB1A7 plasmid (June 18, 2008).

Protocol changes:

  -3 uL of DNA
  -spin down 200 uL of cells and resuspend in 100 uL of LB; plate on LB + amp


July 3, 2008

Nathan Puhl, Munima, Christa, Alix, Roxanne, Sebastian

Checked transformation plates. Only the positive control (pSB1A7) had colonies (~1500) indicating that there is nothing wrong with the transformation protocol or cells so we must be having problems with the DNA extraction from the filter paper. Next week we will attempt various changes to the protocol to extract more DNA.