Hot-Start J-Taq DNA Polymerase (40 U/μL)
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Hot-Start J-Taq DNA Polymerase (40 U/μL)

Cat.No: IVDRM-0102 Datasheet

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Product Name Hot-Start J-Taq DNA Polymerase (40 U/μL)
Catalog No. IVDRM-0102
Description Hot-Start J-Taq DNA Polymerase (40 U/μL) is an antibody-modified, hot-start mutant Taq DNA polymerase. The antibody-blocked enzyme delivers excellent amplification sensitivity and specificity. The blocking antibody is completely inactivated after 30 seconds of heating at the pre-denaturation temperature, releasing full DNA polymerase activity. This hot-start Taq effectively suppresses amplification resulting from non-specific primer annealing during reaction setup and initial heating.
Intended Use Hot-start PCR amplification requiring high specificity and sensitivity; suitable for bulk formulation in molecular reagent manufacturing.
Principle / Technology Antibody-based hot-start mechanism: polymerase activity is blocked by a specific antibody at low temperatures, preventing non-specific primer annealing and extension during reaction setup. Heating at the pre-denaturation temperature for 30 seconds completely inactivates the antibody and restores full polymerase activity.
Sample Type DNA templates for PCR amplification.
Performance Range / Specifications Concentration: 40 U/μL
Blocking antibody fully inactivated after 30 sec at pre-denaturation temperature
Specificity Antibody-mediated hot start effectively suppresses amplification from non-specific primer annealing, delivering high amplification specificity and sensitivity.
Reaction Conditions / Protocol Include a pre-denaturation step at the standard pre-denaturation temperature for at least 30 seconds to fully inactivate the blocking antibody and release DNA polymerase activity.
Storage Conditions Store at -20°C.
Shelf Life 2 years when stored at -20°C.
Package Specifications 400 U
4 KU
40 KU
1,000 KU
Concentration 40 U/μL
Shipping Conditions Shipped with ice packs.
Expiration Date / Stability Stable for 2 years at -20°C.
Application Notes / Precautions Ensure the initial pre-denaturation step lasts at least 30 seconds so that the blocking antibody is completely inactivated and full polymerase activity is released.

For research use only, not for clinical use.

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