Team:University of Lethbridge/Notebook/GeneralLabAugst
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8. Spread 100-300 μl onto a plate made with appropriate antibiotic | 8. Spread 100-300 μl onto a plate made with appropriate antibiotic | ||
9. Grow overnight at 37 °C | 9. Grow overnight at 37 °C | ||
+ | |||
+ | ===August 5, 2008=== | ||
+ | ====Nathan Puhl, Alix, Roxanne and highschool students, | ||
+ | |||
+ | -Performed a Gel Extraction. | ||
+ | -Performed a Restriction Digest of the Lac I and DT plasmids. | ||
+ | |||
+ | |||
+ | ===August 6, 2008=== | ||
+ | ====Nathan Puhl, Roxanne, Alix==== | ||
+ | |||
+ | -Ran a 1% Gel with the Lac I and DT restriction products. | ||
+ | -Performed a Gel Extraction of the restriction products using the Qiagen Gel Extraction Kit. |
Revision as of 04:08, 7 August 2008
Contents |
August 03, 2008
Nathan Phillips
Tranformation of pUC19:
1. Thaw E.coli DH5a cells on ice 2. Add pUC19 DNA, pipette gently to mix (1μl of plasmid) 3. Let sit for 30 minutes on ice 4. Incubate cells for 30 seconds at 42oC 5. Incubate cells on ice for 2 min 6. Add 1 mL SOC at room temp 7. Incubate for 1 hour at 37oC on shaker 8. Spread 100-300 μl onto a plate made with appropriate antibiotic 9. Grow overnight at 37 °C
August 5, 2008
====Nathan Puhl, Alix, Roxanne and highschool students,
-Performed a Gel Extraction. -Performed a Restriction Digest of the Lac I and DT plasmids.
August 6, 2008
Nathan Puhl, Roxanne, Alix
-Ran a 1% Gel with the Lac I and DT restriction products. -Performed a Gel Extraction of the restriction products using the Qiagen Gel Extraction Kit.