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KAPA3G Plant PCR Kit

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Properties

Related Categories Genomic DNA Amplification, Molecular Biology, PCR/Amplification, from Plant
usage   50 μL sufficient for 250 reactions (KK7251)
  50 μL sufficient for 500 reactions (KK7252)
shelf life   ≤12 mo.
shipped in   dry ice
storage temp.   −20°C

Description

Packaging

• KAPA3G Plant DNA Polymerase (2.5 U/μL)
• KAPA Plant PCR Buffer (2X) Contains MgCl2 and dNTPs
• MgCl2 (25 mM)

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.

Quality

Each batch of KAPA3G Plant DNA Polymerase is confirmed to contain <2% contaminating protein (Agilent Protein 230 Assay). KAPA3G Plant 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.

Application

• Amplification of fragments up to 5 kb in size from purified plant DNA, extracted with commercial kits or CTAB-based methods
• Direct PCR from leaf discs, seed samples, and other plant tissue types
• PCR from crude plant DNA extracts, prepared from leaf and/or seed material

Features and Benefits

Key features of the KAPA3G Plant PCR Kit include:
• Fast PCR direct from plant tissues such as leaf discs, seeds and crude plant extracts.
• Streamlined workflows for transgenic screening.
• Improved PCR success rates and reproducibility.
• Efficient amplification of long and difficult targets from all sample types.

Amplify long targets from crude samples and purified DNA:

• Amplify fragments up to 5 kb from purified DNA and crude samples
• High yield and specificity with purified DNA and crude samples

Perform direct PCR from a variety of plant species and tissue types:
• Direct PCR with leaf disc or seed as template
• No need for time-consuming DNA extractions

Streamline workflows and improve turnaround times:
• Perform PCR in half the time compared with wild-type enzymes
• Eliminate the need for time-consuming

DNA extractions Improve success rates with novel crude sample plant PCR workflow:
• Use extraction buffer to prepare crude extracts for plant PCR in just 5 minutes
• High success rates with even the most challenging sample types

Quick Notes:
• KAPA3G Plant DNA Polymerase is tolerant to plant-derived PCR inhibitors, and can amplify frompurified DNA, crude extracts, and plant material.
• Optimize reaction conditions using purified DNA before attempting direct or crude sample PCR.
• For direct PCR, use a sampling tool to control the amount of plant material added to the reaction. The use of excessive amounts of crude plant material in PCR is a major cause of direct PCR reaction failure.
• For crude sample PCR, prepare a crude DNA extract using a small amount of plant material in Extraction Buffer (Refer to Section 3: Crude sample PCR), and use 1 μL per 50 μL reaction.
• KAPA Plant PCR Buffer contains MgCl2 (1.5 mM at 1X) and dNTPs (0.2 mM each at 1X). Additional MgCl2(25 mM) is supplied separately for optimization.

General description

KAPA3G Plant PCR Kits are designed for PCR of plant-derived DNA, using either purified DNA or DNA prepared by crude extraction methods (crude sample PCR). In addition, the KAPA3G Plant PCR Kit can be used to amplify DNA from plant material added directly to the PCR (direct PCR). The KAPA3G Plant PCR Kit contains KAPA3G DNA Polymerase, a novel, third-generation (3G) enzyme which was engineered via a process of directed evolution for improved tolerance to common plant-derived PCR inhibitors such as polyphenolics and polysaccharides.The KAPA3G Plant PCR Kits are optimized for fast and efficient amplification of plant DNA from crude samples, DNA-containing carry-over inhibitors from crude extraction methods, and purified DNA.

Other Notes

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

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport

Documents

Certificate of Analysis

Protocols & Articles

Articles

Directed Evolution

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Peer-Reviewed Papers
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