PRODUCT INFORMATION
i-Taq™ DNA Polymerase with Buffer and dNTPs
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PRODUCT INFORMATION
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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.
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