Not available outside of the UK & Ireland.

Application

KAPA2G Robust PCR Kit is suitable for:Amplification of GC- or AT-rich templatesTemplates containing common PCR inhibitors e.g. salts, urea, SDS, or ethanolCrude sample PCR e.g. buccal swabs, cultured mammalian, yeast, or bacterial cellsColony PCRPolymerase chain reaction

Biochem/physiol Actions

KAPA2G Robust DNA polymerase has 5’;→3’; polymerase and 5’;→3’; exonuclease activities, but no 3’;→5’; exonuclease (proofreading) activity. 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. KAPA2G Robust is a highly processive DNA polymerase, capable of amplifying DNA fragments of up to 1 kb in size with a 15 sec/cycle extension time. The use of excessive extension times is likely to result in smearing and nonspecific amplification. For amplicons ﹤1 kb with genomic DNA as a template, 15 sec per cycle should be sufficient for a high yield of the product. In the case of longer amplicons, the time may be increased to a maximum of 60 sec/kb, in 15-sec increments. PCR products generated by KAPA2G Robust are 3’;-dA-tailed and may be cloned into TA cloning vectors.

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 ratesImproved tolerance to common PCR inhibitors Efficient amplification from crude samples Higher yield and sensitivity per unit of enzymeUnrivalled performance in colony PCR Higher yields and improved consistency of PCR direct from E. coli and yeast cellsQuick Notes: KAPA2G Robust PCR Kits with dNTPs 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 inhibitor contaminated 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.

General description

The second-generation KAPA2G Robust DNA Polymerase was evolved 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.

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 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.

Quality

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.