i-Taq™ DNA Polymerase with Buffer and dNTPs

PRODUCT INFORMATION

i-Taq™ DNA Polymerase with Buffer and dNTPs

ManufactureriNtRON Biotechnology Catalogue / SKU25021 Pack / Variant250 Units
Price £58.45 GBP UK pricing

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PRODUCT INFORMATION

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Product typeDNA Polymerases CollectionDNA Polymerases
01 Description, applications & specifications

Description

i-Taq™ DNA Polymerase with Buffer and dNTPs from iNtRON Biotechnology is a highly purified, thermostable DNA polymerase for routine PCR amplification of DNA targets up to approximately 5 kb.

i-Taq™ is a recombinant 94 kDa Taq DNA polymerase derived from the polymerase gene of Thermus aquaticus strain YT-1 and expressed in E. coli. The purification process is designed to remove residual host-derived proteins and DNA that could otherwise contribute to contamination or non-specific amplification.

The enzyme is supplied at a concentration of 5 U/µL together with a 10X PCR Buffer containing MgCl₂, a separate 10X MgCl₂-free PCR Buffer, a dNTP mixture and 25 mM MgCl₂. This flexible component format allows users to perform standard PCR using the MgCl₂-containing buffer or optimise the magnesium concentration for demanding templates and primer sets using the MgCl₂-free buffer and separately supplied MgCl₂ solution.

i-Taq™ DNA Polymerase has optimal DNA synthesis activity at approximately 72°C. It is suitable for amplification from genomic DNA and cDNA templates, routine PCR, RT-PCR-derived cDNA amplification, direct sequencing-related PCR, T/A cloning and PCR assays used for loss-of-heterozygosity or microsatellite-instability research.

As a conventional Taq DNA polymerase, i-Taq™ does not possess 3′→5′ proofreading exonuclease activity and typically produces PCR products with 3′-adenine overhangs. This makes the amplified products suitable for T/A cloning. For applications requiring substantially higher sequence fidelity, a proofreading polymerase such as i-pfu™ or an enzyme blend such as i-MAX™ II should be considered.

Key Features: Standard recombinant Taq DNA polymerase • 94 kDa thermostable enzyme • 5 U/µL concentration • Amplifies DNA targets up to approximately 5 kb • Optimal extension at approximately 72°C • Supplied with dNTP mixture • Includes MgCl₂-containing and MgCl₂-free PCR buffers • Separate MgCl₂ solution for optimisation • Suitable for genomic DNA and cDNA templates • Produces PCR products suitable for T/A cloning • Flexible individual-component format

Template Types: Genomic DNA • cDNA • Plasmid DNA • Purified DNA • Cloned DNA Templates • Other Compatible DNA Templates

Applications: Routine PCR • Genomic DNA PCR • cDNA Amplification • RT-PCR-Related Amplification • Colony PCR • Direct Sequencing-Related PCR • T/A Cloning • Loss-of-Heterozygosity Research • Microsatellite-Instability Research • Other Standard PCR Applications

Research Use: Research Use Only (RUO)

Manufacturer: iNtRON Biotechnology

Technical Specifications

Specification Details
Product Name i-Taq™ DNA Polymerase with Buffer and dNTPs
Catalogue Nos. 25021 / 25022
Available Pack Sizes 250 units / 500 units
Enzyme Concentration 5 U/µL
Enzyme Molecular Weight Approximately 94 kDa
Enzyme Source Recombinant Thermus aquaticus YT-1 DNA polymerase expressed in E. coli
Maximum Amplicon Length Up to approximately 5 kb
Optimal Extension Temperature Approximately 72°C
Recommended Extension Time Approximately 1 minute per kb
Proofreading Activity No 3′→5′ proofreading exonuclease activity
PCR Product Ends Typically generates 3′-adenine overhangs
Cloning Compatibility Suitable for T/A cloning
Supplied PCR Buffers 10X PCR Buffer with 20 mM MgCl₂ and 10X MgCl₂-free PCR Buffer
dNTP Mixture 10 mM total mixture, 2.5 mM of each dNTP
Separate MgCl₂ Solution 25 mM
Hot-Start Capability No; standard Taq DNA polymerase
Storage –20°C
Classification Research Use Only (RUO)
Manufacturer iNtRON Biotechnology

Kit Contents

Component 250 Units – 25021 500 Units – 25022
i-Taq™ DNA Polymerase, 5 U/µL 250 units 500 units
10X PCR Buffer with 20 mM MgCl₂ 1 mL 1 mL
10X MgCl₂-Free PCR Buffer 1 mL 1 mL
dNTP Mixture, 2.5 mM Each 500 µL 1 mL
25 mM MgCl₂ 1 mL 1 mL

Note: Maximum amplicon length and PCR performance depend on template quality, target GC content, primer design, magnesium concentration, cycle conditions and reaction optimisation. For high-fidelity cloning or sequence-critical applications, use an appropriate proofreading polymerase.

TECHNICAL LIBRARY

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