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This genotyping assay uses pyrosequencing technology and is run on the Biotage
PSQ 96MA. The Jackson Laboratory is not posting the complete details of our
pyrosequencing genotyping assays as the primers for pyrosequencing cannot be
used for sequencing using more traditional methods. The wild type and mutant
nucleotides and the flanking DNA sequence are provided below.
Mutant = A
Heterozygote = A/G
Wild type = G
| Primer | 5' Label | Sequence 5' → 3' | 3' Label | Primer Type | Reaction | Note |
|---|---|---|---|---|---|---|
| pIMR141 | CCA CTG TCT TCA GGT AAT A | SEQ | ||||
| pIMR239 | Fluorophore | TAG CTC ACA CAA CCC AGT TTA CTC | Forward | |||
| pIMR240 | AGA TGG CCC ACT GTC TTC A | Reverse |
| Component | Final Concentration |
|---|---|
| ddH2O | |
| Kapa 2G HS buffer | 1.00 |
| MgCl2 | 2.00 |
| dNTPS-kapa | 0.20 |
| pIMR239 | 0.50 |
| pIMR240 | 0.50 |
| Glycerol | 5.00 |
| Kapa 2G HS taq polym | 0.01 |
| DNA |
| Step | Temp °C | Time | Note |
|---|---|---|---|
| 1 | 94.0 | -- | |
| 2 | 94.0 | -- | |
| 3 | 65.0 | -- | -0.5 C per cycle decrease |
| 4 | 68.0 | -- | |
| 5 | -- | repeat steps 2-4 for 10 cycles | |
| 6 | 94.0 | -- | |
| 7 | 60.0 | -- | |
| 8 | 72.0 | -- | |
| 9 | -- | repeat steps 6-8 for 28 cycles | |
| 10 | 72.0 | -- | |
| 11 | 10.0 | -- | hold |