Taqman qPCR protocols are run on a real time PCR instrument. Use an appropriate instrument specific Fluorophore/Quencher combination. The transgene genotype is determined by comparing ΔCt values of each unknown sample against known homozygous and hemizygous controls, using appropriate endogenous references.
Mutant= 116 bp
Wild Type = 100 bp
| Primer | 5' Label | Sequence 5' → 3' | 3' Label | Primer Type | Reaction | Note |
|---|---|---|---|---|---|---|
| 31592 | GCT GTC CTG GAA CTT GCT CT | Common | ||||
| 31593 | GCT GGA GGT GCA AGC CTT TA | Wild type Reverse | ||||
| 31594 | CTC ATC CTA GCT GCC TGG AA | Mutant Reverse | ||||
| 31595 | Fluorophore-1 | TGA GAG ATC TGC TTG CTT CTG | Quencher-1 | WT Probe | ||
| 31596 | Fluorophore-2 | ATG CAG GAG GAG CTG AGG T | Quencher-2 | MUT Probe |
| Component | Final Concentration |
|---|---|
| Kapa Probe Fast QPCR | 1.00 X |
| ddH2O | |
| Primer 1 | 0.40 uM |
| Primer 2 | 0.40 uM |
| Primer 3 | 0.40 uM |
| Wt Probe | 0.15 uM |
| Mutant Probe | 0.15 uM |
| DNA |
| Step | Temp °C | Time | Note |
|---|---|---|---|
| 1 | 95.0 | -- | |
| 2 | 95.0 | -- | |
| 3 | 60.0 | -- | |
| 4 | -- | repeat steps 2-3 for 40 cycles | |
| 5 | 40.0 | -- | Forever |
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