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From 2011.igem.org

7-13-2011

Retrieved gel from cold room and covered with 1x TAE in gel box and heated it (by running the gel with nothing in it)

Prepared Mutagenesis PCR products from last Thursday to be run on Gel

The tubes I made up came from the following:

A = Green/ Blue tubes conatained Dr. Burkett's dNTP's B = Orange tubes contain Dr. Goode's dNTP's

I prepared 8 tubes as follows:

CA  = Pink tube contains 10 microliters of the Control A sample and 2 microliters of loading dye

CB  = Blue tube contains 10 microliters of the Control B sample and 2 microliters of loading dye
              

Rxn 1 A & B = Pink A tube contains 10 microliters of the RXN 1 A sample and 2 microliters of loading dye
              Blue B tube contains 10 microliters of the RXN 1 B sample and 2 microliters of loading dye


Rxn 4 A & B = Pink A tube contains 10 microliters of the RXN 4 A sample and 2 microliters of loading dye
              Blue B tube contains 10 microliters of the RXN 4 B sample and 2 microliters of loading dye

Rxn 5 A & B = Pink A tube contains 10 microliters of the RXN 5 A sample and 2 microliters of loading dye
              Blue B tube contains 10 microliters of the RXN 5 B sample and 2 microliters of loading dye

These 8 tubs are located in the freezer and are ready to be run on the gel. They are in a yellow rack with a pink taped labeled with todays date and iGEM, mutagenesis PCR for gel.

Dr. Goode requested that the gel lanes be filled as follows

1. Ladder

2. CA

3. CB

4. R1A

5. R1B

6. Ladder

7. R4A

8. R4B

9. R5A

10. R5B

--Mduley 18:00, 13 July 2011 (CDT)

Team:Baltimore/Notebook

Hours

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