추천 제품
생물학적 소스
bacterial (Thermus aquaticus BM)
Quality Level
재조합
expressed in E. coli
설명
5 U/βl
Number of Reactions:
If 1.25 U are used per 50 μL reaction, Taq DNA Polymerase, dNTPack is designed for approximately sufficient for number of reactions, mentioned in the usage.
형태
liquid
사용
sufficient for 2,000 reactions (04728904001)
sufficient for 4,000 reactions (04728858001)
sufficient for 400 reactions (04728874001)
sufficient for 80 reactions (04728866001)
sufficient for 800 reactions (04728882001)
분자량
95 kDa
특징
dNTPs included
hotstart: no
포장
pkg of 1,000 U (04728882001 [4 x 250 U])
pkg of 2,500 U (04728904001 [10 x 250 U])
pkg of 5,000 U (04728858001 [20 x 250 U])
pkg of 100 U (04728866001)
pkg of 500 U (04728874001 [2 x 250 U])
제조업체/상표
Roche
농도
0.025 units/reaction
파라미터
72 °C optimum reaction temp.
기술
PCR: suitable
색상
colorless
입력
purified DNA
최적 pH
~9.0 (20 °C)
solubility
water: soluble
적합성
suitable for PCR and automated sequencing reactions
UniProt 수납 번호
응용 분야
genomic analysis
life science and biopharma
외래 활성
endonucleases, none detected
exonuclease, none detected
nicking activitities, none detected
저장 온도
−20°C
일반 설명
Taq DNA Polymerase, 5 U/μl
PCR Buffer, 10x concentrated, with MgCl2
PCR Nucleotide Mix
For maximum convenience, select the ready-to-use 2x concentrated PCR Master.
Taq DNA Polymerase was originally isolated from the thermophilic eubacterium Thermus aquaticus BM, a strain lacking Taq I restriction endonuclease. The enzyme preparation obtained from E.coli is free of nonspecific engo- or exonucleases according to the current quality control procedures.
애플리케이션
- PCR
- RT-PCR
- Other primer-extension reactions, such as sequencing and labeling
특징 및 장점
- Reliable reproducible results: High lot-to-lot consistency.
- No need to test each lot: Taq DNA Polymerase is rigorously tested.
- Prevent PCR carryover: dUTP incorporation combination with Uracil-DNA Glycosylase prevents PCR cross-contamination.
포장
품질
단위 정의
Unit Assay: Incubation buffer:
67 mM Tris/HCl; pH 8.3/25 °C, 5 mM MgCl2, 10 mM Mercaptoethanol, 0.2% Polydocanol, 0.2 mg/ml Gelatine, 0.2 mM each dATP, dGTP, dTTP and 0.1 mM dCTP.
Incubation procedure:
M13mp9ss, M13 primer (17mer) and 1 μCi (α-32P) dCTP are incubated with suitable dilutions of Taq DNA Polymerase in 50 μl incubation buffer at +65 °C for 60 minutes. The amount of incorporated dNTPs is determined by trichloroacetic acid precipitation.
Volume Activity: 5 U/μl
저장 및 안정성
kept upright to prevent leakage
기타 정보
Lack of restriction endonuclease:
The enzyme originally isolated from T. aquaticus BM lacks Taq I restriction endonuclease activity.
법적 정보
키트 구성품 전용
- Taq DNA Polymerase 5 U/μl
- PCR Buffer with MgCl<sub>2</sub> 10x concentrated
- PCR Nucleotide Mix
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.
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