Horse-Power™ Taq DNA Polymerase, MasterMix
Horse-Power™ Taq DNA Polymerase MasterMix (2x) is a ready-to-use, optimized PCR Master Mix containing TruePure™ dNTPs, Mg²⁺, buffer, and thermostable Taq DNA Polymerase.
Manufactured under ISO 13485 and ISO 9001 certified facilities, it ensures lot-to-lot consistency, reproducibility, and outstanding performance.
Simply add primers and template — no extra components required.
Horse Power™ Taq DNA Polymerase MasterMix is a ready-to-use 2× mix containing all necessary components for routine PCR amplification. It offers high specificity, strong yields, and reliable reproducibility.
The formulation simplifies PCR setup, reducing pipetting steps and minimizing contamination risk. It ensures consistent results across a broad range of DNA templates.
The optimized 2× formulation saves time and minimizes the risk of contamination by reducing pipetting steps. Each lot is produced in ISO 13485 and ISO 9001 certified facilities, guaranteeing consistent quality and reliable amplification performance for both research (RUO) and diagnostic (IVD) applications.
Have questions or require under IVD Grade? Contact us
Price: 78.00 € – 899.00 €
Detailed information:
Advantages & Features
- eliable: consistent results across batches thanks to strict QC and manufacturing control.
- Highest purity: enzyme ≥ 98 %, ultra-low residual DNA, minimal secondary activities, and low bioburden
- ISO certified: produced under ISO 13485 & ISO 9001 quality systems.
- Highly efficient enzyme: exceptional activity, specificity, and thermostability.
- Customizable: Available in different concentrations, bulk, and Lyophilization-friendly format. Contact us
- Thermostable: enzyme half-life ≈ 40 min at 94 °C.
- A-tailing capability: adds 3′-adenine overhangs for TA cloning.
- Modified nucleotide incorporation: supports biotinylated and fluorescent nucleotides.
- Convenient: complete PCR mix (only primers and DNA required).
- Molecular weight: 94 kDa.
Specifications
Includes
P0035: 250 rxn* Horse-Power™ Taq DNA Polymerase Master Mix (2x)
P0036: 10,000 rxn* Horse-Power™ Taq DNA Polymerase Master Mix (2x)
*Includes all necessary reagents except template and primer DNA.
Download documentation
Datasheet MSDSBrochureApplications
- Routine amplifications. PCR and qPCR.
- Colony screening (see Horse-Power™ Red DNA Polymerase).
- Amplification of plasmid, viral, or genomic DNA templates (up to 5 kb).
- Amplification of mixed DNA templates.
- Incorporation of labeled or modified nucleotides.
- PCR product generation for TA or GC cloning.
Tables & Figures
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Quality Control
- Functionally tested in PCR.
- Ultra-low residual host DNA (by qPCR).
- Exempt of nucleases (endo-, exo, and ribonucleases) activities guaranteed by appropriate quality tests.
- Control of Bioburden.
Advice
Storage, Shipping & Guarantee
- Shipped in: Gel pack.
- Storage: -20 °C.
Citations
- Díaz, P. A., Baldrich, Á. M., Rodríguez, F., Díaz, M., Álvarez, G., Pérez-Santos, I., … & Reguera, B. (2024). Mesodinium–Dinophysis encounters: temporal and spatial constraints on Dinophysis blooms.
- U. Tillmann, M. Gottschling, I. Sunesen, S. Wietkamp, N. Dzhembekova, F. Rodriguez Hernández, J. Tardivo Kubis, E. Sar, M. Kaufmann & M. Hoppenrath (2024). Morphological and molecular characterization of Prorocentrum bidens (formerly known as P. compressum) and description of the closely related Prorocentrum bisaeptum sp. nov. (Prorocentrales, Dinophyceae). Phycologia
- Angelova, G., Stefanova, P., Brazkova, M., & Krastanov, A. (2023). Molecular and morphological characterization of Xylaria karsticola (Ascomycota) isolated from the fruiting body of Macrolepiota procera (Basidiomycota) from Bulgaria. Plos one, 18(6), e0287679.
- Petrova, S., & Petkova, M. (2023). Plant Traits of Tilia tomentosa Moench, Fraxinus excelsior L., and Pinus nigra JF Arnold as a Proxy of Urbanization. Forests, 14(4), 800.
- Mwangi, Z., Naeku, G., Mureithi, M., Onyambu, F., & Bulimo, W. (2022). Mutation patterns of resistance genes for macrolides, aminoglycosides, and rifampicin in nontuberculous mycobacteria isolates from Kenya. F1000Research, 11(962), 962.
- Petkova, M., Gotcheva, V., Dimova, M., Bartkiene, E., Rocha, J. M., & Angelov, A. (2022). Screening of Lactiplantibacillus plantarum Strains from Sourdoughs for Biosuppression of Pseudomonas syringae pv. syringae and Botrytis cinerea in Table Grapes. Microorganisms, 10(11), 2094.
- Petkova, M., Spasova-Apostolova, V., Masheva, V., Atanasova, D., & Tahsin, N. (2021). Endophytic colonization of Solanaceае family plants by fungal entomopathogen Beauveria bassiana strain 339 to control Colorado potato beetle (Leptinotarsa decemlineata Say). Bulgarian Journal of Agricultural Science, 27, 1.
- Petkova, Mariana, et al. “Isolation and Characterization of Lactic Acid Bacteria and Yeasts from Typical Bulgarian Sourdoughs.” Microorganisms 9.7 (2021): 1346.
- Rodriguez-Sanchez, A., Margareto, A., Robledo-Mahon, T., Aranda, E., Diaz-Cruz, S., Gonzalez-Lopez, J., … & Gonzalez-Martinez, A. (2017). Performance and bacterial community structure of a granular autotrophic nitrogen removal bioreactor amended with high antibiotic concentrations.Chemical Engineering Journal.
- Ruiz Carrascoso, G. (2016). Características microbiológicas y clínico-epidemiológicas de enterobacterias productoras de carbapenemasa oxa-48 en el contexto de un brote hospitalario (Doctoral dissertation, Universidad Complutense de Madrid).
Safety Statements
This product is Manufactured by Canvax Reagents SLU, in facilities certified ISO13485 and ISO9001 and according to cGMP following ICHQ7. For further processing in clinical or diagnostic applications, but not suitable for administration to humans or animals.
For more info, please check its Material Safety Data Sheet
MSDS
Customers Review
FAQs
1 review for Horse-Power™ Taq DNA Polymerase, MasterMix
Carlos Mendez –
In our teaching laboratory, we use this MasterMix for routine end-point PCR with undergraduate students. Having the mix pre-formulated reduces pipetting steps and minimizes setup errors during practical sessions. The reactions perform consistently under standard cycling parameters, which is important when multiple groups run samples simultaneously. It has made training new students much smoother.