Matt:LabNotes/2013-6-6
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Sequence Agilent Oligos
PCR
PCR Mix
Reaction of 0 gap probes:
Components | Volume |
10nM Agilent Expansion PCRd 0 gap Oligos | 0.40 |
100uM Forward ISB_AP1V6_AFv1 | 0.40 |
100uM Reverse ISB_AP2V6_AR | 0.40 |
2x KAPA SYBG fast MM | 50 |
H2O | 49 |
Total | 100.2 |
Reaction of 20 gap probes:
Components | Volume |
10nM Agilent Expansion PCRd 20 gap Oligos | 0.40 |
100uM Forward ISB_AP1V4_AFv1 | 0.40 |
100uM Reverse ISB_AP2V4_AR | 0.40 |
2x KAPA SYBG fast MM | 50 |
H2O | 49 |
Total | 100.2 |
Agilent Oligos: Expansion PCRd but before Production PCR (see: http://genome-tech.ucsd.edu/LabNotes/index.php/Matt:LabNotes/2013-5-10)
Program 98C 30s -> (98C 5s -> 50C 20s -> 72C 30s)x5 -> (98C 5s -> 72C 30s)x10 -> 72C 3min
- Did same number of PCR cycles as Production PCR to keep amplification as consistent as possible
- Took out Dan's samples after 13 cycles
Tube # | Probes (0.4ul) | Forward Primer 100uM (0.4ul) | Reverse Primer 100uM (0.4ul) | Total Cycles |
1 | 0gap 10nM | ISB_AP1V6_AFv1 | ISB_AP2V6_AR | 15 |
2 | 20gap 10nM | ISB_AP1V4_AFv1 | ISB_AP2V4_AR | 15 |
3 | #1-V6 20nM | ISB_AP1V6_AFv2 | ISB_AP2V6_AR | 13 |
4 | #1-V4 20nM | ISB_AP1V4_AFv2 | ISB_AP2V4_AR | 13 |
5 | #2-V6 20nM | ISB_AP1V6_AFv1 | ISB_AP2V6_AR | 13 |
6 | #2-V4 20nM | ISB_AP1V4_AFv1 | ISB_AP2V4_AR | 13 |
7 | #3-V6 20nM | ISB_AP1V6_AFv2 | ISB_AP2V6_AR | 13 |
8 | #3-V4 20nM | ISB_AP1V4_AFv2 | ISB_AP2V4_AR | 13 |
9 | #4-V6 20nM | ISB_AP1V6_AFv1 | ISB_AP2V6_AR | 13 |
10 | #4-V4 20nM | ISB_AP1V4_AFv1 | ISB_AP2V4_AR | 13 |
*First made 9X Master Mix of KAPA and H2O: 450ul KAPA + 441ul H2O