추천 제품
Grade
Molecular Biology
Quality Level
형태
liquid
사용
sufficient for ≤1,250 reactions (04738403001)
sufficient for ≤2,500 reactions (04738420001)
sufficient for ≤250 reactions (04738357001)
sufficient for ≤50 reactions (04738314001)
sufficient for ≤500 reactions (04738381001)
특이 활성도
5 U/μL
포장
pkg of 1,000 U (04738381001 [4x250 U])
pkg of 2,500 U (04738403001 [10x250 U])
pkg of 5,000 U (04738420001 [20x250 U])
pkg of 100 U (04738314001)
pkg of 500 U (04738357001 [2x250 U])
제조업체/상표
Roche
농도
40 U/mL
55 U/mL
파라미터
72 °C optimum reaction temp.
기술
DNA amplification: suitable
PCR: suitable
색상
colorless
pH
8.0-9.0
solubility
water: miscible
적합성
suitable for molecular biology
응용 분야
life science and biopharma
외래 활성
nicking activity, none detected (up to 10U w.pBR 322-DNA)
ribonuclease, none detected
unspecified endonuclease, none detected
저장 온도
−20°C
일반 설명
애플리케이션
- Hot start PCR up to 3 kb
- Hot Start RT-PCR up to 3 kb
- Multiplex PCR
- Difficult templates, e.g., secondary structures or GC-rich sequences
- Automated PCR, e.g., handling at room temperatures
- quantitaive PCR(qPCR)
For maximum convenience, select the 2x concentrated ready-to-use FastStart PCR Master.
특징 및 장점
Each dNTPack contains 10 mM additive-free sodium salt nucleotides as a ready-to-use mix.
- Higher specificity, sensitivity, and yield:
- Use robotic setup.
- Prevent PCR carryover contamination.
- Cost-effective.
포장
품질
For details please refer to the respective Instruction for Use.
단위 정의
Unit Assay: 1 μg M13mp9ss DNA, 0.3 μg M13 sequencing primer and 0.1 μCi [α--32P] dCTP are incubated with varying amounts of units of FastStart Taq DNA Polymerase in 50 μl incubation buffer at 65 °C for 60 min. The amount of incorporated dNTPs is determined.
Volume Activity: 5 U/μl
저장 및 안정성
기타 정보
Hot start protocols improve PCR specificity, sensitivity, and yield. Heat-labile blocking groups make the modified enzyme inactive at +15 to +25°C. No elongation occurs when primers bind nonspecifically. The enzyme is activated by removing the blocking groups at +95°C for 2 to 6 minutes. PCR products with 3′-single A overhangs are produced, ideal for T/A cloning. For PCR carryover prevention, use the PCR Nucleotide MixPLUS and Uracil-DNA Glycosidase, heat-labile.
법적 정보
키트 구성품 전용
- FastStart Taq DNA Polymerase, in storage and dilution buffer 5 U/μl
- PCR Reaction Buffer, with 20 mM MgCl2 10x concentrated
- PCR Reaction Buffer, without MgCl2 10x concentrated
- MgCl2 Stock Solution 25 mM
- GC-RICH Solution 5x concentrated
- PCR Nucleotide Mix
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
문서
PCR success relies on enzyme, buffer choice, template purity, primer concentration, and nucleotide quality.
The purpose of Hot Start PCR is to inhibit the PCR reaction in order to reduce nonspecific amplification, prevent the formation of primer dimers, and increase product yields.
핫스타트(Hot Start) PCR의 목적은 비특이적 증폭을 줄이고 프라이머 이량체의 형성을 방지하며 제품 수율을 높이기 위해 PCR 반응을 억제하는 것입니다.
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