PFORCEKB
Roche
KAPA PROBE FORCE
2 ×, Universal
Synonyma:
qPCR
About This Item
Doporučené produkty
Quality Level
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
- GMO testing
- Mouse transgenics
- SNP genotyping
- Food/water pathogen detection
- Infectious disease research
- Cancer research
- DNA quantification
- Quantitative polymerase chain reaction (qPCR)
- Digital droplet PCR
- For amplification of templates directly from cDNA synthesis reactions
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.
Quality
Preparation Note
Other Notes
Pouze součásti soupravy
- KAPA3G HotStart® DNA Polymerase
- dNTPs (including dUTP)
- MgCl2 4.5 mM at 1X
- ROX™ reference dye
- stabilizers
Storage Class
12 - Non Combustible Liquids
wgk_germany
WGK 1
flash_point_f
does not flash
flash_point_c
does not flash
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