Wednesday, July 13

From 2011.igem.org

(Difference between revisions)
(7-13-2011)
(7-13-2011)
 
(One intermediate revision not shown)
Line 12: Line 12:
I prepared 8 tubes as follows:
I prepared 8 tubes as follows:
    
    
-
CA  = Pink tube contains 10 microliters of the Control A sample and 2 microliters of loading dye
+
<nowiki>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
CB  = Blue tube contains 10 microliters of the Control B sample and 2 microliters of loading dye
Line 25: Line 25:
Rxn 5 A & B = Pink A tube contains 10 microliters of the RXN 5 A 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
+
               Blue B tube contains 10 microliters of the RXN 5 B sample and 2 microliters of loading dye</nowiki>
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.
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.
Line 33: Line 33:
1.  Ladder
1.  Ladder
 +
2.  CA
2.  CA
 +
3.  CB
3.  CB
 +
4.  R1A
4.  R1A
 +
5.  R1B
5.  R1B
 +
6.  Ladder
6.  Ladder
 +
7.  R4A
7.  R4A
 +
8.  R4B
8.  R4B
 +
9.  R5A
9.  R5A
 +
10. R5B
10. R5B

Latest revision as of 00:40, 15 July 2011

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