Difference between revisions of "Team:UCLA/Notebook/Honeybee Silk/14 July 2015"
(→Double Digestion of Purified PCR Product) |
(→PCR of Lac promoter/SIlk/Spycatcher) |
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Both samples were sent in for sequencing. | Both samples were sent in for sequencing. | ||
| − | ='''PCR of Lac promoter/ | + | ='''PCR of Lac promoter/Silk/Spycatcher'''= |
*Using primer 3 and 4 that contain overhangs with the Biobrick prefix and suffix. | *Using primer 3 and 4 that contain overhangs with the Biobrick prefix and suffix. | ||
Revision as of 20:46, 15 July 2015
Contents
Miniprep
Samples 1 and 3 (inoculated) were miniprepped using the Zymo Plasmid Miniprep Kit.
OD
- 128.23 ng/uL
- 106.85 ng/uL
Both samples were sent in for sequencing.
PCR of Lac promoter/Silk/Spycatcher
- Using primer 3 and 4 that contain overhangs with the Biobrick prefix and suffix.
| Component | Volume (out of 50uL) |
|---|---|
| 5X Q5 Reaction Buffer | 10uL |
| 10mM dNTPS | 1uL |
| 10mM primer 3 | 2.5uL |
| 10mM primer 4 | 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 | 72C | 20s |
| Extension | 72C | 30s |
| Final Extension | 72C | 2min |
| Hold | 12C | Hold |
Gel Visualization and Purification
I ran the PCR product on a 1% agarose gel, expected size ~1600bp
Results: There was a band at the appropriate length and another band, probably the result of non-specific binding. The correct band was extracted and purified using the Qiagen Gel Purification kit.
OD: 88.12ng/uL
Double Digestion of Purified PCR Product
- The insert will be digested with EcoRI and Pst1 for preparation for ligation into the psb1c3 backbone (already digested with PstI and EcoRI).
| Component | Volume (out of 50uL) |
|---|---|
| NEB Buffer 2.1 | 5uL |
| EcoRI | 1uL |
| PstI | 1uL |
| Purified Insert | 9uL |
| Nuclease Free Water | 34uL |
Program
| Step | Temperature | Time |
|---|---|---|
| Incubation | 37C | 1 hour |
| Heat Inactivation | 80C | 15 min |
| Hold | 10C | Hold |
Calculating Competency
- Calculating competency of cells prepared on 7/12.
- Equation = # colonies / ug DNA plated
- Using 2 ul of 50pg/ul puc19 vector to transform in to 50 ul
- Counted 300 colonies
- plated 1x10^-5 ug (1/10 of transformation reaction).
- Therefore tranformation efficiency = 3 x 10^7 cfu/ug DNA