추천 제품
일반 설명
KAPA Taq is supplied in a 2X ReadyMix™ format containing all the components required for PCR except primers and template. Simply use PCR-grade water to make up the required reaction volume. KAPA Taq Buffer A (and KAPA Taq Buffer with dye) are standard Tris-ammonium sulfate-based buffers, while KAPA Taq Buffer B is a Tris-potassium chloride buffer, which allows convenient direct analysis of the PCR product by agarose gel electrophoresis after cycling. All KAPA Taq Buffers are 10X buffers, containing 15 mM MgCl2 (1.5 mM at 1X). KAPA Taq DNA Polymerase may be used in combination with any standard Taq buffer with a pH of 8.3 or higher.
애플리케이션
KAPA Taq PCR Kit with dNTPs has been used in:
- High throughput PCR
- Amplification of low copy DNA templates
- Multiplex PCR
- Specific amplification of complex templates
- RT-PCR
- Quantitative polymerase chain reaction (qPCR)
생화학적/생리학적 작용
KAPA Taq DNA Polymerase is based on the single-subunit, wild-type Taq DNA polymerase of the thermophilic bacterium Thermus aquaticus. 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.
특징 및 장점
High performance
Quick Notes:
- Improved sensitivity, specificity, and yields.
- Novel buffer formulation facilitates specific primer annealing, leading to higher yield of specific product.
Quick Notes:
- KAPA Taq HotStart® DNA Polymerase can replace any commercial hotstart Taq DNA polymerase in an existing protocol. The final MgCl2 concentration and annealing temperature may need to be optimized to account for differences in formulation.
- The KAPA Taq HotStart Buffer is a uniquelyformulated buffer offering improved specificity and sensitivity, and improved amplification of GC- and AT-rich templates.
- The KAPA Taq HotStart Buffer does not contain MgCl2; MgCl2 (25 mM) is supplied separately to allow greater flexibility during reaction setup.
- The KAPA Taq HotStart PCR Kit is suitable for the amplification of fragments up to 3.5 kb from genomic DNA or 5 kb from less complex targets.
품질
Each batch of KAPA Taq HotStart DNA Polymerase is confirmed to contain <2% contaminating protein (Agilent Protein 230 Assay). KAPA Taq HotStart PCR kits 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
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 DNA Polymerase 5 U/µL
- 10X KAPA Taq Buffer A
- 10X KAPA Taq Buffer B
- MgCl2 25 mM
- KAPA dNTP Mix 10 mM each
Storage Class Code
12 - Non Combustible Liquids
WGK
WGK 1
Flash Point (°F)
does not flash
Flash Point (°C)
does not flash
이미 열람한 고객
Marco L Leung et al.
Genome biology, 16, 55-55 (2015-04-09)
Single-cell genome sequencing methods are challenged by poor physical coverage and high error rates, making it difficult to distinguish real biological variants from technical artifacts. To address this problem, we developed a method called SNES that combines flow-sorting of single
Dispersion quality of amine functionalized multiwall carbon nanotubes plays critical roles in polymerase chain reaction enhancement.
Yuce M and Hikmet B
Journal of Nanoparticle Research, 16(12), 2768-2768 (2014)
Li-Li Guo et al.
Experimental and therapeutic medicine, 15(6), 5394-5402 (2018-05-31)
Viral vectors represent a potential strategy for the treatment of human malignant tumors. Currently, recombinant adenovirus vectors are commonly used as gene therapy vehicles, as it possesses a proven safety profile in normal human cells. The recombinant adenovirus system has
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.