CA6 PCR #2 7/10/19 - testing BAS
E1 E2 E3 E4 E5 E6 E7 - test
Procedure
Samples E1 E2 E3 E4 E5 E6 E7 were used in this PCR (polimerase chain reaction) reaction
First A Master Mix of water, 2x mytaq mix, CA6.38R Primer (concentration: 10 micromolar), CA6.38L Primer (concentration: 10 micromolar)
| Component | Volume for 14 reactions(+5% error) |
|---|---|
| Water | 132.3 micoleters |
| 2x mytaq mix | 183.75 micoleters |
| CA6.38R Primer (concentration: 10 micromolar) | 14.7 micoleters |
| CA6.38L Primer (concentration: 10 micromolar) | 14.7 micoleters |
| BAS (Borine Serum Albumin) | 1 microliter |
added BAS to mix BAS stops certain things that caninhibit PCRs
24 micoleters of this master mix was added to 14 tubes For the 2 negative controls 12.5 micoleters water and 12.5 micoleters mytaq mix were added there was no positive control was available
1 microleter of the DNA samples was added to the coresponding tube
The first tube was placed into a thermomixer with the following settings
| Step | Temperature | Duration | cycles |
|---|---|---|---|
| 1 | 92°C | 3:00 | 1 |
| 2 | 92°C | 0:30 | 35 |
| 3 | 55°C | 1:00 | 35 |
| 4 | 72°C | 0:15 | 35 |
| 5 | 72°C | 2:00 | 1 |
| 6 | 4°C | hold | - |
the second tube had the cycles increased to 45
| Step | Temperature | Duration | cycles |
|---|---|---|---|
| 1 | 92°C | 3:00 | 1 |
| 2 | 92°C | 0:30 | 45 |
| 3 | 55°C | 1:00 | 45 |
| 4 | 72°C | 0:15 | 45 |
| 5 | 72°C | 2:00 | 1 |
| 6 | 4°C | hold | - |
these amplified DNA samples were then tested by making a gel
to create the Gel the following steps were taken
1.5g agarose and 75ml 1X TAE buffer were mixed to make a 2% agarose 75ml gel mix the mix was microwaved and swirled until there were no flakes then 1 microliters Gelgreen was added
the mix was left to cool for 5 minutes then poured into the gel mold the gel was left to harden for 30 minutes
once hardened enough Used TAE buffer was poured into the gel box to cover the mold
5 microliter aliquots of DNA samples E1 E2 E3 E4 E5 E6 E7 and the two controls were made 1 microliter of 5x loading dye was added to each
First 3 microliters of the HyperLadder 100bp was added to the first well of the mold then the DNA samples were each added to the wells in the following order
| Ladder | E1 | E2 | E3 | Negative Control | E4 | E5 | E6 | E7 |
| Ladder | E1 | E2 | E3 | Negative Control | E4 | E5 | E6 | E7 |
The voltage was set to 100V and run for 60 minutes
This is the resulting Gel
