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2GRKB

Roche

KAPA2G Robust PCR Kit

Synonyme(s) :

PCR

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About This Item

Code UNSPSC :
41106300
Nomenclature NACRES :
NA.55

Utilisation

sufficient for 200 reactions
sufficient for 500 reactions

Niveau de qualité

Durée de conservation

≤12 mo.

Caractéristiques

Difficult Templates/Specialty Enzymes PCR
dNTPs included
hotstart: no

Conditionnement

pkg of 100 U (KK5023)
pkg of 250 U (KK5024)

Fabricant/nom de marque

Roche

Technique(s)

PCR: suitable

Entrée

crude DNA

Température de stockage

−20°C

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Description générale

The second-generation KAPA2G Robust DNA Polymerase was evolved to solve inconsistent amplification across a broad range of amplicon types (GC- and AT-rich). KAPA2G Robust PCR Kit enables higher processivity and specific activity, which translates to robust PCR performance, high sensitivity, and improved tolerance to common inhibitors. The high performance of the KAPA2G Robust DNA Polymerase is ideally suited for challenging PCR applications and difficult samples, eliminating the need for optimization using multiple enzymes and protocols.
The enzyme is supplied with three reaction buffers, and a proprietary enhancer for GC-rich PCR. KAPA2G Buffer A is specifically formulated for the unique characteristics of the engineered KAPA2G enzymes, while KAPA2G Buffer B is recommended when template samples are contaminated with PCR inhibitors. KAPA2G GC Buffer is recommended for GC-rich PCR, while KAPA Enhancer 1, a proprietary DNA destabilizer, may be combined with either KAPA2G Buffer A or B in GC-rich assays, or assays where secondary structure is problematic.

Application

KAPA2G Robust PCR Kit has been used for:
  • Amplification of GC- or AT-rich templates and gene amplification
  • Templates containing common PCR inhibitors e.g. salts, urea, SDS, or ethanol
  • Crude sample PCR e.g. buccal swabs, cultured mammalian, yeast, or bacterial cells
  • Colony PCR
  • Routine PCR
  • PCR amplification
  • Avipoxvirus specific PCR
  • Simplex PCR
  • Semi-quantitative PCR

Actions biochimiques/physiologiques

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

Caractéristiques et avantages

Efficient amplification of GC- and AT-rich targets
  • Robust performance across a wide range of GC- and AT-rich templates
  • Increased PCR success rates

Improved tolerance to common PCR inhibitors
  • Efficient amplification from crude samples
  • Higher yield and sensitivity per unit of enzyme

Unrivalled performance in colony PCR
  • Higher yields and improved consistency of PCR direct from E. coli and yeast cells

Quick Notes:
  • KAPA2G Robust PCR Kits contain KAPA2G Robust DNA Polymerase, engineered for high processivity and inhibitor tolerance.
  • Both purified genomic DNA and crude samples (e.g. colony PCR) can be used as template.
  • Use 0.5 U of KAPA2G Robust DNA Polymerase per 25 μL reaction. More challenging PCRs (GCrich,crude sample) may require higher enzyme concentrations.
  • Use 15 sec/kb extension time per cycle, and increase to 30–60 sec/kb for difficult amplicons or templates.
  • KAPA2G Buffers contain 1.5 mM MgCl2 at 1X.
  • Additional MgCl2 may be added using the 25 mM MgCl2 solution provided in the kit.
  • KAPA2G Buffer A is optimized for high yield, specificity, and sensitivity.
  • KAPA2G Buffer B is recommended for inhibitorcontaminated template samples.
  • KAPA2G GC Buffer is recommended for GC-rich PCR (>70% GC).
  • KAPA Enhancer 1 can be used with KAPA2G Buffer A or B, particularly for GC-rich assays.
  • Reaction products are 3′-dA-tailed and may be cloned into TA cloning vectors.

Qualité

Each batch of KAPA2G Robust DNA Polymerase is confirmed to contain <2% contaminating protein (Agilent Protein 230 Assay). KAPA2G Robust 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.

Notes préparatoires

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 all components have 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.

Autres remarques

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

Composants de kit seuls

Réf. du produit
Description

  • KAPA2G Robust Standard or HotStart® DNA Polymerase 5 U/μL

  • 5X KAPA2G Buffer A with MgCl2

  • 5X KAPA2G Buffer B with MgCl2

  • 5X KAPA2G GC Buffer with MgCl2

  • 5X KAPA Enhancer 1

  • MgCl2 25 mM

Pictogrammes

Exclamation markHealth hazard

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Acute Tox. 4 Oral - Aquatic Chronic 3 - STOT SE 2

Code de la classe de stockage

12 - Non Combustible Liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

does not flash

Point d'éclair (°C)

does not flash


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Consulter la Bibliothèque de documents

Michal Vinkler et al.
Genetica, 143(1), 101-112 (2015-01-30)
Toll-like receptors (TLRs) are a cornerstone of vertebrate innate immunity. In this study, we identified orthologues of TLR4, TLR5 and TLR7 (representing both bacterial- and viral-sensing TLRs) in the grey partridge (Perdix perdix), a European Galliform game bird species. The
Multiplex amplicon sequencing for microbe identification in community-based culture collections.
Armanhi J S L, et al.
Scientific Reports, 6, 29543-29543 (2016)
Guillaume Croville et al.
Journal of virological methods, 261, 34-39 (2018-08-08)
Avian pox is an infectious disease caused by avipoxviruses (APV), resulting in cutaneous and/or tracheal lesions. Poxviruses share large genome sizes (from 130 to 360 kb), featuring repetitions, deletions or insertions as a result of a long-term recombination history. The increasing
Martin Kircher et al.
Nature communications, 10(1), 3583-3583 (2019-08-10)
The majority of common variants associated with common diseases, as well as an unknown proportion of causal mutations for rare diseases, fall in noncoding regions of the genome. Although catalogs of noncoding regulatory elements are steadily improving, we have a
Vasso Skouridou et al.
Food chemistry, 287, 354-362 (2019-03-13)
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