Difference between revisions of "Team:UCLA/Notebook/Honeybee Silk/8 July 2015"
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The sample was loaded onto a 1% agarose gel with 10uL 6X loading dye against a 1kB ladder. | The sample was loaded onto a 1% agarose gel with 10uL 6X loading dye against a 1kB ladder. | ||
Expected band size: ~1000bp | Expected band size: ~1000bp | ||
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+ | Results: | ||
− | + | [[File:Gel 2015-07-08.jpg|none|thumb|500px|Gel image]] |
Latest revision as of 20:14, 15 July 2015
Contents
Inoculation of 5/19 Transformation
Recent experiments have proven that the pET24a miniprepped sample was not correct. Today I will repick colonies and grow them up for miniprepping.
I picked two colonies from the 1:1 kanamycin plate and suspended them in 100uL ddH2O. Each sample was incubated at 37C with 5mL LB broth and 5uL 1000X kanamycin.
PCR of Honeybee G-block and Purification
The concentration obtained after digestion and purification was too low (20.12ng/uL), today I will be redoing the PCR, digestion, and purification to obtain a higher yield.
Component | Volume (out of 50uL) |
---|---|
5X Q5 Reaction Buffer | 10uL |
10mM dNTPS | 1uL |
10mM primer 10 | 2.5uL |
10mM primer 11 | 2.5uL |
Template (Honeybee G-block) | 1uL |
Q5 High Fidelity DNA Polymerase | 0.5uL |
Nuclease Free Water | 32.5uL |
Program
Step | Temperature | Time |
---|---|---|
Initial Denaturation | 98C | 30s |
Cycles (x25) | 98C | 10s |
Annealing | 67C | 20s |
Extension | 72C | 30s |
Final Extension | 72C | 2min |
Hold | 12C | Hold |
The sample was then purified using the Zymo DNA Concentrate and Cleanup Kit. OD: 283.09ng/uL
Digestion and Purification
Component | Volume (out of 50uL) |
---|---|
NEB 2.1 Buffer | 5uL |
BamHI | 1uL |
NdeI | 1uL |
PCR Purified Honeybee G-block | 5uL |
Nuclease Free Water | 38uL |
Program
Step | Temperature | Time |
---|---|---|
Incubation | 37C | 1 hour |
Heat Inactivation | 80C | 15 min |
Hold | 10C | Hold |
The sample was loaded onto a 1% agarose gel with 10uL 6X loading dye against a 1kB ladder.
Expected band size: ~1000bp
Results: