추천 제품
Quality Level
사용
sufficient for 100 reactions
20 μL sufficient for 100 reactions
sufficient for 500 reactions
20 μL sufficient for 500 reactions
유통기한
≤12 mo.
특징
dNTPs included
hotstart
포장
kit of 1 mL (100 x 20 μL rxn; KK4300)
kit of 5 mL (500 x 20 μL rxn; KK4301)
제조업체/상표
Roche
농도
2 ×
기술
qPCR: suitable
입력
crude DNA
검출 방법
probe-based
저장 온도
−20°C
일반 설명
KAPA PROBE FORCE is a highly inhibitor resistant qPCR master mix that removes the need for DNA purification, enabling streamlined sample-to-Cq workflows. The master mix contains a third generation DNA polymerase evolved to overcome blood, tissue, and plant PCR inhibitors. Crude samples can now be analyzed with comparable accuracy, reproducibility, and sensitivity as purified DNA using KAPA PROBE FORCE.
- 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
애플리케이션
KAPA PROBE FORCE has been used for:
- 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
특징 및 장점
Streamline sample-to-Cq workflows in <1 hour:
Generate accurate and reproducible results:
Break through high levels of qPCR inhibitors:
Multiplex crude samples efficiently:
Quick Notes:
- 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.
품질
KAPA PROBE FORCE qPCR Master Mix Universal is subjected to stringent functional quality control, free of detectable contaminating exo- and endonuclease activities, and meets strict requirements with respect to DNA contamination.
제조 메모
ROX reference dye is sensitive to light exposure. Always ensure that the product has been fully thawed and mixed before use. Avoid repeated freezing and thawing.
기타 정보
For Research Use Only. Not for use in diagnostic procedures.
키트 구성품 전용
제품 번호
설명
- KAPA3G HotStart® DNA Polymerase
- dNTPs (including dUTP)
- MgCl2 4.5 mM at 1X
- ROX™ reference dye
- stabilizers
Storage Class Code
12 - Non Combustible Liquids
WGK
WGK 1
Flash Point (°F)
does not flash
Flash Point (°C)
does not flash
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
Cancer reports (Hoboken, N.J.), 3(3), e1248-e1248 (2020-07-17)
Ductal carcinoma in situ (DCIS) comprises a diverse group of preinvasive lesions in the breast and poses a considerable clinical challenge due to lack of markers of progression. Genomic alterations are to a large extent similar in DCIS and invasive
Development of genotyping method for functionally relevant variants of cytochromes P450 in cynomolgus macaques.
Journal of Veterinary Pharmacology and Therapeutics, 41(1), e30-e34 (2018)
Clarity? digital PCR system: a novel platform for absolute quantification of nucleic acids.
Analytical and Bioanalytical Chemistry, 409(7), 1869-1875 (2017)
Plant disease, 102(9), 1748-1758 (2018-08-21)
Current management of sudden death syndrome (SDS) of soybean, caused by Fusarium virguliforme, focuses on planting resistant varieties and improving soil drainage; however, these measures are not completely effective. A 6-year study evaluated the effects of cropping system diversification on
문서
An overview of directed evolution and the methods for generating proteins with optimized or entirely new functions.
자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..
고객지원팀으로 연락바랍니다.