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Merck

TAQKB

Roche

KAPA Taq PCR Kit

別名:

PCR, Taq

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About This Item

UNSPSCコード:
41106300
NACRES:
NA.54

シェルフライフ

≤18 mo.

品質水準

特徴

dNTPs included: no
hotstart: no

包装

pkg of 250 U (KK1014)
pkg of 2500 U (BK1000)
pkg of 500 U (KK1015)
pkg of 5000 U (BK1002)

メーカー/製品名

Roche

テクニック

PCR: suitable

入力

purified DNA

保管温度

−20°C

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アプリケーション

KAPA Taq PCR Kit has been used in:
  • High throughput PCR
  • Amplification of low copy DNA templates
  • Multiplex PCR
  • Specific amplification of complex templates
  • RT-PCR
  • random amplified polymorphic DNA polymerase chain reaction (RAPD-PCR)
  • Polymerase chain reaction (PCR)
  • Genotyping

生物化学的/生理学的作用

KAPA Taq PCR Kit, which contains 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.

特徴および利点

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 DNA Polymerase can replace any commercial Taq DNA polymerase in an existing protocol.
  • The final MgCl2 concentration may need to be optimized to account for differences in buffer formulation.
  • KAPA Taq Buffers contain MgCl2 at a final concentration of 1.5 mM. Buffer A is recommended as first approach and for applications requiring high yields. Buffer B is recommended for applications where high sensitivity is required (e.g. when the template is limiting). Both buffers may be evaluated to determine the buffer most suitable for a specific application.
  • 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.

品質

Each batch of KAPA Taq DNA Polymerase is confirmed to contain <2% contaminating protein (Agilent Protein 230Assay). KAPA Taq Ready Mixes 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.

調製ノート

Always ensure that the product has been fully thawed and mixed before use. Reagents may be stored at 4°C forshort-term use (up to 1 month). Return to -20°C for long term storage.

その他情報

For Research Use Only. Not for use in diagnostic procedures.

法的情報

HOTSTART is a registered trademark of Molecular BioProducts, Inc.

キットの構成要素のみ

製品番号
詳細

  • KAPA Taq Standard or HotStart® DNA Polymerase 5 U/μL

  • 10X KAPA Taq Buffer A

  • 10X KAPA Taq Buffer B

  • MgCl2 25 mM

保管分類コード

12 - Non Combustible Liquids

WGK

WGK 1

引火点(°F)

does not flash

引火点(℃)

does not flash


試験成績書(COA)

製品のロット番号・バッチ番号を入力して、試験成績書(COA) を検索できます。ロット番号・バッチ番号は、製品ラベルに「Lot」または「Batch」に続いて記載されています。

以前この製品を購入いただいたことがある場合

文書ライブラリで、最近購入した製品の文書を検索できます。

文書ライブラリにアクセスする

SNES: single nucleus exome sequencing
Marco L Leung
Genome Biology, 16(55) (2015)
Direct conversion of mouse embryonic fibroblasts into functional keratinocytes through transient expression of pluripotency-related genes.
Iacovides D, et al.
Stem Cell Research & Therapy, 7(1), 98-98 (2016)
Improvement of poly-[gamma]-glutamic acid (PGA) producing Bacillus subtilis SBMYP-1 by N-methyl-N′-nitro-N-nitrosoguanidine (NTG) mutagenesis.
Mahidsanan T and Gasaluck P
International food research journal., 23(2), 751-751 (2016)
Demetris Iacovides et al.
Data in brief, 20, 1602-1606 (2018-09-29)
We have performed whole transcriptome sequencing of 5-FU resistant and 5-FU sensitive tumors generated in a mouse model of de novo carcinogenesis that closely recapitulates tumor initiation, progression and maintenance in vivo. Tumors were generated using the DMBA/TPA model of
Charalambos Loizides et al.
PloS one, 10(12), e0143840-e0143840 (2015-12-10)
Tumorigenesis is a complex, multistep process that depends on numerous alterations within the cell and contribution from the surrounding stroma. The ability to model macroscopic tumor evolution with high fidelity may contribute to better predictive tools for designing tumor therapy

資料

An overview of directed evolution and the methods for generating proteins with optimized or entirely new functions.

ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.

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