Difference between revisions of "Team:UCLA/Notebook/Honeybee Silk/13 July 2015"
(→Colony PCR of 7/12 Transformation) |
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| 9uL | | 9uL | ||
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| + | =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 [https://www.neb.com/protocols/1/01/01/high-efficiency-transformation-protocol-c2987 this NEB protocol] to transform with our BL21 cells. | ||
Revision as of 01:34, 14 July 2015
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 25L) |
|---|---|
| APEX Taq Red Mastermix | 12.5uL |
| 10mM primer 10 | 1.25uL |
| 10mM primer 11 | 1.25uL |
| Transformed Cells | 1uL |
| Nuclease Free Water | 9uL |
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.