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🍁 CSR Hot Start Taq DNA Polymerase, with 10X Reaction Buffer (no dNTPs)

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CSR Hot Start Taq DNA Polymerase reliably amplifies a wide variety of DNA templates—including mouse, human, plasmid, and bisulfite-converted DNA—producing... Read more

$99.00

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    Description

    CSR Hot Start Taq DNA Polymerase reliably amplifies a wide variety of DNA templates—including mouse, human, plasmid, and bisulfite-converted DNA—producing consistent PCR products. This polymerase leaves a 3′ adenine overhang, making the products well-suited for TA cloning. Verified extension capabilities reach up to 5,000 base pairs, with speeds of up to 1 kb per minute.

    Hot Start Technology
    Hot Start Taq DNA Polymerase contains an aptamer based Hot Start technology that prevents amplification during PCR setup and minimizes the amplification of primer-dimer and nonspecific products. Initial incubation at 94 - 95 °C is NOT required. The aptamer contains a 3’ cap that prevents its amplification and ensures no interference with cloning or any downstream analysis.

    🍁 Researched, Developed and Manufactured in London, ON, Canada.


     Catalogue Number Units Number of Reactions
    M0202-010 1000 U 400
    M0202-050 5000 U 2000
    M0202-500 50,000 U 20,000

     

    Included in the Kit
    • 10X PCR Buffer
    • 50 mM Magnesium Sulfate
    • GC Extender (For GC-rich templates and difficult templates)
    • Protocol
    Features
    • Generates PCR product with 3'-dA overhangs
    • The error rate in PCR is 2.2 x 10-5 errors per nucleotide per cycle
    • Generates PCR product of up to 5 kb
    • Aptamer based Hot Start provides a reversible inhibition of non-specific PCR products
    • Stable at room temperature for up to 2 weeks
    Applications
    • Effective in routine and high throughput PCR
    • Incorporates modified nucleotides in PCR
    • Effective in DNA labeling

    Documents

    1. Product Information Sheet
    2. Quick Guide Sheet
    3. SDS Sheet

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


    Specifications

    • Species of Origin: Thermus aquaticus
    • Enzyme Type: Thermostable DNA polymerase
    • 5’->3′ Exonuclease Activity: Yes
    • “A” Overhang: Yes
    • 3’->5′ Exonuclease Activity: No
    • Processivity Rate: 1 Kbp / minute
    • Unit Definition: One unit incorporates 10 nmol of dNTP into acid-precipitable material in 30 minutes at 74°C.
    • Amplification Limit: Confirmed to 5 Kbp
    • Enzyme Concentration: 5 units/ÂľL
    • Read more

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