추천 제품
생물학적 소스
microbial (Pyrococcus woesei)
Quality Level
형태
liquid
사용
sufficient for ≤200 reactions (11644955001)
sufficient for 200 reactions
sufficient for ≤40 reactions (11644947001)
sufficient for 40 reactions
특이 활성도
≥5000 U/mL
분자량
90 kDa
특징
High Fidelity PCR
dNTPs included: no
hotstart: no
포장
pkg of 100 U (11644947001)
pkg of 500 U (11644955001 [2 x 250 U])
제조업체/상표
Roche
농도
2.5 units/reaction
기술
PCR: suitable
색상
colorless
입력
purified DNA
solubility
water: soluble
적합성
suitable for enzyme test
응용 분야
genomic analysis
life science and biopharma
외래 활성
Endonucleases with lambda-DNA 30 units, none detected
Nicking act using pBR322-DNA ≤30 units, none detected
저장 온도
−20°C
일반 설명
The use of Pwo DNA Polymerase during PCR significantly reduces the occurrence of random amplification errors.
애플리케이션
- Due to its proofreading activity, the thermostable Pwo DNA Polymerase has an extremely low error rate, 18-fold lower compared to Taq DNA Polymerase. It is therefore ideal for applications that require the highest possible fidelity in DNA synthesis. It can be applied for High fidelity PCR
- Cloning of PCR products
- Characterization of rare mutations
- PCR
특징 및 장점
- Excellent accuracy (18-fold more accurate than Taq DNA polymerase)
- High thermal stability
- Nearly as processive as Taq DNA polymerase
- Accepts modified nucleotides
포장
품질
- Activity: The enzyme is tested on activated DNA.
- Function: The enzyme is tested in two PCRs, using λDNA and human genomic DNA as templates.
- Proofreading ability: Proofreading activity is assayed according to the laq Iq fidelity assay [Frey, B. & Suppmann, B. (1995) Biochemica 2. 8-9].
- Absence of nucleases: The enzyme is tested on various substrates to ensure the absence of detectable endonucleases, exonucleases, and nicking activity according to the current Quality Control procedures.
단위 정의
Unit Assay: Incubation buffer for assay on activated DNA
20 mM Tris-HCl, pH 8.8 (20 °C), 50 mM KCl, 2.5 mM MgCl2, 10 mM 2-mercaptoethanol, 0.2 mM of each dATP, dCTP, dGTP, dTTP.
Incubation procedure
12.5 mg activated calf thymus DNA and 0.1 mCi [α-32P]dCTP are incubated with 0.01 to 0.1 U Pwo DNA Polymerase in 50 μl incubation buffer with a paraffin oil overlay at +70 °C for 30 minutes. The amount of incorporated dNTPs is determined by trichloroacetic acid precipitation followed by scintillation counting.
Volume Activity: 5 U/μl
제조 메모
Modified nucleotides are substrates
Pwo DNA Polymerase accepts modified nucleotides like digoxigenin-dUTP, biotin-dUTP, or fluorescein-dUTP. Thus, it can add these nucleotides to DNA during PCR. These nonradioactively labeled products can be used as a hybridization probe in many applications.
Magnesium concentration
If you use the magnesium-containing reaction buffer supplied with the enzyme, the final MgCl2 concentration in the PCR will be 2.0mM. For other magnesium concentrations (e.g., for optimizing the reaction to accommodate a particular template), use the magnesium-free reaction buffer and add appropriate amounts of the magnesium stock.
저장 및 안정성
kept upright to prevent leakage
기타 정보
법적 정보
키트 구성품 전용
- Enzyme is supplied in storage and dilution buffer
- PCR buffer, with 20 mM MgSO4 10x concentrated
- PCR buffer, without MgSO4 10x concentrated
- MgSO4 stock solution
유해 및 위험 성명서
예방조치 성명서
Hazard Classifications
Aquatic Chronic 3
Storage Class Code
12 - Non Combustible Liquids
WGK
WGK 2
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
자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..
고객지원팀으로 연락바랍니다.