추천 제품
사용
50 μL sufficient for 250 reactions
Quality Level
유통기한
≤18 mo.
특징
dNTPs included
hotstart: no
포장
pkg of 6.25 mL
제조업체/상표
Roche
농도
2 ×
기술
PCR: suitable
입력
purified DNA
저장 온도
−20°C
일반 설명
KAPA Taq DNA Polymerase is a single-subunit Taq DNA polymerase from the thermophilic bacterium Thermus aquaticus, purified from recombinant Escherichia coli. KAPA Taq ReadyMix™ (2X) is a ready-to-use cocktail containing all components for PCR, except primers and template. KAPA Taq ReadyMix is available with and without dye. The 2X ReadyMix with dye consists of two inert tracking dyes to permit direct loading of PCR products onto agarose gels for analysis by electrophoresis, without adding a DNA loading solution. KAPA Taq and KAPA Taq HotStart® DNA Polymerase have 5′→3′ polymerase and 5→′3′ exonuclease activities, but no 3′ → 5′ exonuclease (proofreading) activity. The enzyme has an error rate of approximately 1 error per 2.2 x 105 nucleotides incorporated. In the hot start formulation, the KAPA Taq is combined with a proprietary antibody that inactivates the enzyme until the first denaturation step, eliminating spurious amplification products and increasing reaction efficiency and sensitivity.
애플리케이션
KAPA Taq ReadyMix™ with dye has been used in:
- high throughput PCR
- the amplification of low copy DNA templates
- multiplex PCR
- specific amplification of complex templates
- RT-PCR
- nested PCR (nPCR)
- amplifying exome 23 of anaplastic lymphoma kinase (ALK)
- polymerase chain reaction (PCR) amplification
생화학적/생리학적 작용
KAPA Taq DNA Polymerase has 5′→3′ polymerase and 5′→3′ exonuclease activity. It does not elicit a 3′→5′ exonuclease (proofreading) activity. This enzyme system has an error rate of approximately 1 error per 2.2 X 105 nucleotides incorporated. PCR products created with KAPA Taq are A-tailed and are appropriate for cloning into TA cloning vectors.
특징 및 장점
Key Features:
High performance:
Quick Notes:
High performance:
- Improved sensitivity, specificity, and yields
- Novel buffer formulation facilitates specific primer annealing, leading to higher yield of specific product
Quick Notes:
- KAPA Taq ReadyMix™ can replace any commercial Taq DNA polymerase in an existing protocol. The annealing temperature may need to be optimized to account for differences in formulation.
- The KAPA Taq PCR system is suitable for the amplification of fragments up to 3.5 kb from genomic DNA or 5 kb from less complex targets.
- The 2X KAPA Taq ReadyMix with dye includes two inert tracking dyes, which allow loading of PCR products directly onto agarose gels for analysis.
- KAPA Taq ReadyMixes contain 1.5 mM MgCl2 and 0.2 mM of each dNTP (at 1X).
품질
Each batch of KAPA Taq DNA Polymerase is confirmed to contain <2% contaminating protein (Agilent Protein 230 Assay). KAPA Taq ReadyMixes are subjected to stringent quality control tests, are free of contaminating exo- and endonuclease activity, and meet strict requirements with respect to DNA contamination levels.
제조 메모
Handling:
Always ensure that the product has been fully thawed and mixed before use. Reagents may be stored at 4°C for short-term use (up to 1 month). Return to -20°C for long-term storage.
Always ensure that the product has been fully thawed and mixed before use. Reagents may be stored at 4°C for short-term use (up to 1 month). Return to -20°C for long-term storage.
기타 정보
For Research Use Only. Not for use in diagnostic procedures.
법적 정보
HOTSTART is a registered trademark of Molecular BioProducts, Inc.
ReadyMix is a trademark of Sigma-Aldrich Co. LLC
키트 구성품 전용
제품 번호
설명
- KAPA Taq Standard or HotStart® DNA Polymerase 5 U/μL
- 10X KAPA Taq Buffer A
- 10X KAPA Taq Buffer B
- 10X KAPA Buffer with loading dye
- 5X KAPA Taq HotStart® Buffer (HotStart® kits only)
- MgCl2 25 mM
- dNTP Mix (optional) 10 mM each
- Stabilizers
모두 보기 (8)
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
Non-typhoidal Salmonella DNA traces in gallbladder cancer.
Infectious Agents and Cancer, 11(1), 12-12 (2016)
문서
An overview of directed evolution and the methods for generating proteins with optimized or entirely new functions.
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