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About This Item
usage
sufficient for 100 reactions, 20 μL sufficient for 100 reactions, sufficient for 500 reactions, 20 μL sufficient for 500 reactions
shelf life
≤12 mo.
feature
dNTPs included, hotstart
packaging
kit of 1 mL (100 x 20 μL rxn; KK4300), kit of 5 mL (500 x 20 μL rxn; KK4301)
manufacturer/tradename
Roche
concentration
2 ×
technique(s)
qPCR: suitable
input
crude DNA
detection method
probe-based
storage temp.
−20°C
General description
- Direct qPCR from crude blood, tissue, and plant extracts
- Sample-to-Cq workflows in <1 hour
- High efficiency for accurate, reproducible, and sensitive results
- Superior tolerance to carry-over inhibitors
- Multiplex compatibility with crude extracts
Application
Features and Benefits
- Eliminate the time and cost of sample purification by amplifying directly from crude samples
- Analyze a wide range of sample types including whole blood, cells, mouse tails, FFPE, leaf, stem, seed, and soil
Generate accurate and reproducible results:
- Kits include a third-generation DNA polymerase, evolved for robust target amplification and detection
- Enzyme maintains high reaction efficiency in the presence of PCR inhibitors for reliable data generation
Break through high levels of qPCR inhibitors:
- Achieve greater levels of sensitivity for inhibited blood, tissue, and plant samples
- Convert purified DNA assays to crude workflows without observable Cq delays
Multiplex crude samples efficiently:
- Accelerate genotyping analysis with single reaction allelic discrimination of crude DNA extracts
- Maximize data collection from precious samples, increase throughput, and reduce costs
Quick Notes:
- This kit contains the KAPA3G HotStart DNA Polymerase enzyme, enabling probe-based qPCR for both routine and challenging sample types.
- Initial denaturation of 3 min at 98°C is recommended to ensure complete denaturation of complex target DNA. A 5-min denaturation time may be required for some crude samples.
- For two-step cycling, use a 20-sec combined annealing/extension/data acquisition at 60°C as a first approach.
- A 10-sec annealing/extension/data acquisition time may be used with most assays, but this must be determined empirically.
- For crude samples, the amount of sample in the reaction may be reduced to improve performance, but this must be determined empirically.
Preparation Note
Analysis Note
Other Notes
1 of 1
This Item | |||
|---|---|---|---|
| technique(s) qPCR: suitable | technique(s) qPCR: suitable | technique(s) qPCR: suitable | technique(s) qPCR: suitable |
| feature dNTPs included, hotstart | feature dNTPs included, hotstart | feature - | feature dNTPs included, hotstart |
| usage sufficient for 100 reactions, sufficient for 500 reactions, 20 μL sufficient for 100 reactions, 20 μL sufficient for 500 reactions | usage sufficient for 100 reactions, sufficient for 1000 reactions, sufficient for 500 reactions, sufficient for 5000 reactions | usage - | usage sufficient for 100 reactions, sufficient for 1000 reactions, sufficient for 500 reactions |
| detection method probe-based | detection method probe-based | detection method - | detection method probe-based |
| concentration 2 × | concentration 2 × | concentration 2 × | concentration 2 × |
| manufacturer/tradename Roche | manufacturer/tradename Roche | manufacturer/tradename Roche | manufacturer/tradename Roche |
Kit Components Only
- KAPA3G HotStart® DNA Polymerase
- dNTPs (including dUTP)
- MgCl2 4.5 mM at 1X
- ROX™ reference dye
- stabilizers
Storage Class
12 - Non Combustible Liquids
wgk
WGK 1
flash_point_f
does not flash
flash_point_c
does not flash
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Related Content
Global Trade Item Number
| SKU | GTIN |
|---|---|
| KK4301 | 04061837905407 |
| KK4300 | 04061837905391 |

