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Merck

2GFMPXKB

Roche

KAPA2G Fast Multiplex Mix

suitable for PCR, 2 ×

別名:

PCR, multiplex, multiplex PCR

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この商品について

NACRES:
NA.55
UNSPSC Code:
41106300
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製品名

KAPA2G Fast Multiplex Mix, suitable for PCR, 2 ×

shelf life

≤12 mo.

packaging

kit of 1.25 mL (100 x 25 μL rxn; KK5801)
kit of 6.25 mL (500 x 25 μL rxn; KK5802)

manufacturer/tradename

Roche

concentration

2 ×

technique(s)

PCR: suitable

storage temp.

−20°C

Quality Level

Analysis Note

Each batch of KAPA2G Fast HotStart DNA Polymerase is confirmed to contain <2% contaminating protein (AgilentProtein 230 Assay). KAPA2G Fast Multiplex 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 contaminationlevels.

Application

KAPA2G Fast Multiplex Mix has been used for:
  • Typing of transgenic organisms
  • Amplification of microsatellites
  • Typing and detection of pathogens
  • Amplification of multiple DNA fragments for single nucleotide polymorphism (SNP) genotyping
  • Semi-quantitative PCR
  • 3-plex PCR

Biochem/physiol Actions

DNA fragments generated with KAPA2G Fast DNA Polymerase have the same characteristics as DNA fragments generated with wild-type Taq DNA polymerase, and may be used for sequencing, restriction enzyme digestion and cloning. Like wild-type Taq, KAPA2G Fast has 5′→3′ polymerase and 5′→3′ exonuclease activities, but no 3′→5′ exonuclease (proofreading) activity. The fidelity of KAPA2G Fast is similar to that of wild-type Taq; it has an error rate of approximately 1 error per 1.7 x 105 nucleotides incorporated. PCR products generated with KAPA2G Fast are 3′-dA-tailed and may be cloned into TA cloning vectors.

Features and Benefits

Improve sensitivity, specificity, and yields
  • Uniform representation of all amplicons
  • Successful multiplex PCR with difficult, GC-rich targets

Increase speed without compromising performance
  • 60% reduction in cycling time
  • Extension times as low as 15 seconds

Quick Notes:
  • KAPA2G Fast Multiplex Mix contains the engineered KAPA2G Fast HotStart DNA Polymerase, for fastand efficient multiplex PCR.
  • The KAPA2G Fast Multiplex Mix contains a buffer optimized for multiplex PCR, with 0.2 mM of each dNTP and 3 mM MgCl2 (at 1X).
  • Use 0.2 μM of each primer, and 10–100 ng of template DNA per reaction.
  • Anneal at 60°C for 30 seconds.
  • Perform extension for 15 sec, and increase for longer amplicons, and/or highly multiplexed reactions.

General description

KAPA2G Fast Multiplex PCR Kits contain a second-generation (2G) enzyme derived through a process of directed evolution. KAPA2G FAST HotStart® DNA Polymerase is an antibody-mediated hot start formulation engineered for higher processivity and speed, offering significantly faster extension rates than wild-type Taq DNA polymerase. In addition to speed, KAPA2G Fast provides higher yields and sensitivity than competitor enzymes, allowing for more uniform multiplexed PCR.
KAPA2G Fast HotStart PCR Kits are designed for fast PCR, in which total reaction times are 20–70% shorter than those of conventional PCR assays performed with wild-type Taq DNA polymerase. This can be achieved without sacrificing reaction performance and does not require specialized PCR consumables or thermocyclers.

Other Notes

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

Preparation Note

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. Provided that the ReadyMix has been handled carefully and not contaminated, the kit is not expected to be compromised if left (unintentionally) at room temperature for a short period of time (up to 3 days). Long-term storage at room temperature and 4°C is not recommended. Please note that reagents stored at temperatures above -20°C are more prone to degradation when contaminated during use, and therefore storage at such temperatures is at the user′s own risk.

Legal Information

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

  • KAPA2G Fast HotStart® DNA Polymerase

  • Reaction buffer

  • dNTPs

  • MgCl2 3 mM

pictograms

Exclamation markHealth hazard

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - STOT SE 2

保管分類

12 - Non Combustible Liquids

wgk

WGK 1

flash_point_f

does not flash

flash_point_c

does not flash


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Sungsik Kim et al.
Genome biology, 19(1), 158-158 (2018-10-10)
Spatial mapping of genomic data to tissue context in a high-throughput and high-resolution manner has been challenging due to technical limitations. Here, we describe PHLI-seq, a novel approach that enables high-throughput isolation and genome-wide sequence analysis of single cells or
Pellets of proof: First glimpse of the dietary composition of adult odonates as revealed by metabarcoding of feces.
Kaunisto K M, et al.
Ecology and Evolution, 7(20), 8588-8598 (2017)
Precise manipulation of bacterial chromosomes by conjugative assembly genome engineering.
Ma N J, et al.
Nature Protocols, 9(10), 2285-2285 (2014)
Kostas A Papavassiliou et al.
Journal of cellular and molecular medicine, 23(9), 6215-6227 (2019-06-30)
Polycystic Kidney Disease (PKD), which is attributable to mutations in the PKD1 and PKD2 genes encoding polycystin-1 (PC1) and polycystin-2 (PC2) respectively, shares common cellular defects with cancer, such as uncontrolled cell proliferation, abnormal differentiation and increased apoptosis. Interestingly, PC1
Ilianna Zoi et al.
Breast cancer research : BCR, 21(1), 132-132 (2019-12-05)
ERBB-2 is overexpressed in about 20% of breast cancers (BCs), indicating poor prognosis. The receptor activator of nuclear factor-κB (RANK) pathway is implicated in ERBB-2 (+) BC. The purpose of this study was to elucidate the underlying molecular mechanism of

資料

指向性進化の概要と最適化された、またはまったく新しい機能を有するタンパク質の生成方法。

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

プロトコル

Robust Taq DNA polymerase reagents and PCR kits for efficient extraction, purification, and amplification of routine and challenging DNA template sequences.

通常のおよび増幅困難なDNAテンプレート配列の効率的な抽出、精製、増幅のためのロバストなTaq DNAポリメラーゼ試薬とPCRキット。

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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