Difference between revisions of "Team:UCLA/Notebook/Honeybee Silk/13 July 2015"
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Expected band sizes: ~1000bp | Expected band sizes: ~1000bp | ||
+ | Samples 1 and 3 had bright bands at the appropriate base pair length. | ||
− | + | (sorry need to export images as jpeg) | |
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+ | ='''Inoculation'''= | ||
+ | |||
+ | The remaining 99uL of samples 1 and 3 were inoculated with 5mL LB broth and 5uL 1000X kanamycin, incubated at 37C. | ||
=Testing competency of BL21 cells from 7/12= | =Testing competency of BL21 cells from 7/12= |
Revision as of 20:34, 14 July 2015
Contents
Colony PCR of 7/12 Transformation
- The transformation was successful for the 3:1 ligated products plates. I picked 3 colonies off the plate and suspended each in 100uL of ddH2O.
- Using APEX Taq Red Mastermix
Component | Volume (out of 25uL) |
---|---|
APEX Taq Red Mastermix | 12.5uL |
10mM primer 10 | 1.25uL |
10mM primer 11 | 1.25uL |
Transformed Cells | 1uL |
Nuclease Free Water | 9uL |
Program
Step | Temperature | Time |
---|---|---|
Initial Denaturation | 95C | 30s |
Cycles(x30) | 95C | 10s |
Annealing | 67C | 20s |
Extension | 70C | 30s |
Final Extension | 70C | 2 min |
Hold | 14C | Hold |
Visualization
I ran each of the sample on a 1% agarose gel against a 1kB ladder for 20 minutes. Expected band sizes: ~1000bp
Samples 1 and 3 had bright bands at the appropriate base pair length.
(sorry need to export images as jpeg)
Inoculation
The remaining 99uL of samples 1 and 3 were inoculated with 5mL LB broth and 5uL 1000X kanamycin, incubated at 37C.
Testing competency of BL21 cells from 7/12
- Used puc 19 vector at 50 picograms/ul to test transformation efficiency.
- Added 2 ul of puc 19 to 50 ul of competent BL21 cells
- Used this NEB protocol to transform with our BL21 cells.
- Plated 10% of the cells on a warm amp plate and put plate in at 4 pm 7/13