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Roche

KAPA2G Robust HotStart PCR Kit

with dNTPs

Synonym(s):

PCR, hotstart PCR

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About This Item

UNSPSC Code:
41106300
NACRES:
NA.55

Quality Level

usage

sufficient for 1000 reactions
sufficient for 200 reactions
sufficient for 500 reactions

shelf life

≤12 mo.

feature

Difficult Templates/Specialty Enzymes PCR
dNTPs included
hotstart

packaging

pkg of 100 U (KK5532)
pkg of 250 U (KK5516)
pkg of 500 U (KK5518)

manufacturer/tradename

Roche

technique(s)

PCR: suitable

input

crude DNA

storage temp.

−20°C

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General description

The second-generation KAPA2G Robust DNA Polymerase evolves to solve inconsistent amplification across a broad range of amplicon types (GC- and AT-rich). This product 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.

Application

KAPA2G Robust HotStart® PCR Kit has been used for:
  • Amplification of GC- or AT-rich templates
  • 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
  • qPCR
  • Nested polymerase chain reaction (PCR) amplification
  • Amplification of DNA targets in PCR
  • DNA amplification using conventional PCR
  • Routine PCR

Biochem/physiol Actions

DNA fragments created with KAPA2G Robust HotStart® DNA Polymerase have the same characteristics as DNA fragments generated with wild-type Taq DNA polymerase. It can be used for routine downstream applications, such as restriction enzyme digestion, cloning, and sequencing. Like wild-type Taq, KAPA2G Robust HotStart has 5′→3′ polymerase and 5′→3′ exonuclease activities, devoid of 3′→5′ exonuclease (proofreading) activity. The fidelity of KAPA2G Robust HotStart is similar to wild-type Taq. It shows an error rate of approximately 1 error per 1.7 x 105 nucleotides incorporated.

Features and Benefits

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 HotStart® PCR Kits with dNTPs contain KAPA2G Robust HotStart 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 HotStart 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.

Quality

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

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 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.

Other Notes

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

Legal Information

HOTSTART is a registered trademark of Molecular BioProducts, Inc.

Kit Components Only

Product No.
Description

  • KAPA2G Robust HotStart® DNA Polymerase 5 U/µL

  • 5X KAPA2G Buffer A

  • 5X KAPA2G Buffer B

  • 5X KAPA2G GC Buffer

  • 5X KAPA Enhancer 1

  • KAPA MgCl2 25 mM

  • KAPA dNTP Mix 10 mM each

Pictograms

Exclamation markHealth hazard

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 1

Flash Point(F)

does not flash

Flash Point(C)

does not flash


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Areli de la Cruz-de la Cruz et al.
Diagnostic microbiology and infectious disease, 97(4), 115075-115075 (2020-06-14)
Formalin-fixed paraffin-embedded (FFPE) tissues are a source of biological material for molecular studies; several methods to extract DNA from FFPE tissues have been reported. This process is challenging because of formaldehyde-induced cross-linking between proteins and DNA as well as molecule
Xuan Chen et al.
Archives of gynecology and obstetrics, 298(6), 1219-1227 (2018-09-27)
Grb10 is a key imprinted gene that is suspected to have a role in the adverse outcomes of assisted reproductive technology (ART), but little is known about the effects of ART on it. Primary ART techniques, including superovulation, in vitro
Jani J Sormunen et al.
Experimental & applied acarology, 70(4), 491-500 (2016-11-05)
Anaplasma phagocytophilum is the causative agent of an emerging tick-borne disease, human granulocytic anaplasmosis. While the bacterium has been reported from questing ticks in neighboring Sweden, Norway and Russia, the few surveys regarding questing ticks in Finland have thus far
Han Yih Lau et al.
Scientific reports, 7, 38896-38896 (2017-01-18)
Developing quick and sensitive molecular diagnostics for plant pathogen detection is challenging. Herein, a nanoparticle based electrochemical biosensor was developed for rapid and sensitive detection of plant pathogen DNA on disposable screen-printed carbon electrodes. This 60 min assay relied on the
Anaplasma phagocytophilum in questing Ixodes ricinus ticks in southwestern Finland.
Sormunen J J, et al.
Experimental & Applied Acarology, 70(4), 491-500 (2016)

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