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OnePCR SuperMix (50 uL for each total RXN volume)

OnePCR™ is a ready-to-use PCR reaction mixture. Simply add primers, template, and water, the reagent will execute primer extensions and other molecular biology applications. OnePCR™ is a pre-mixed solution containing Taq DNA polymerase, PCR Buffer, dNTP, gel loading dyes, and fluorescence dye.OnePCR™ which contains the Taq DNA polymerase, is purified from the E. coli., and expressing the Thermus aquaticus DNA polymerase gene. This enzyme has a 5′ → 3′ DNA polymerase and the 5′ → 3′ exonuclease activity but lacks the 3′ → 5′ exonuclease activity. OnePCR™, which contains the fluorescence dye, is directly detected on BLooK LED transilluminator or UV epi-illuminator after the DNA electrophoresis. OnePCR™ mixture is supplied at the 2X concentration to allow approximately 50% of the final reaction volume to be used for the addition of primer and template solutions.Reagents are provided with the sufficient amplification reactions of 50 μl each.

100 in stock

100 in stock

OnePCR™ is a ready-to-use PCR reaction mixture. Simply add primers, template, and water, the reagent will execute primer extensions and other molecular biology applications. OnePCR™ is a pre-mixed solution containing Taq DNA polymerase, PCR Buffer, dNTP, gel loading dyes, and fluorescence dye.OnePCR™ which contains the Taq DNA polymerase, is purified from the E. coli., and expressing the Thermus aquaticus DNA polymerase gene. This enzyme has a 5′ → 3′ DNA polymerase and the 5′ → 3′ exonuclease activity but lacks the 3′ → 5′ exonuclease activity. OnePCR™, which contains the fluorescence dye, is directly detected on BLooK LED transilluminator or UV epi-illuminator after the DNA electrophoresis. OnePCR™ mixture is supplied at the 2X concentration to allow approximately 50% of the final reaction volume to be used for the addition of primer and template solutions.Reagents are provided with the sufficient amplification reactions of 50 μl each.

MB203-0100
100 rxns (2.5 mL)
Ambient temperature
Store at -20°C

R.U.O

Rebih, N., Boutaiba, S., Aboualchamat, G., Souttou, K., Hakem, A., & Al Nahhas, S. (2020). Molecular and epidemiological characterization of Giardia intestinalis assemblages detected in Djelfa, Algeria. Journal of Parasitic Diseases, 44(2), 281-288. Tasanapak, K., Kucharoenphaibul, S., Wongwigkarn, J., Sitthisak, S., Thummeepak, R., Chaibenjawong, P., … & Nimanussornkul, K. (2023). Prevalence and virulence genes of Staphylococcus aureus from food contact surfaces in Thai restaurants. PeerJ, 11, e15824. EL-Mahdi, M. B. M. Sequence Variances and Phylogenetic Relationship among Seven River Nile Teleostei Species from Qena, Egypt using Partial Mitochondrial Cytochrome-b Gene Sequences.

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OnePCR SuperMix (50 uL for each total RXN volume)

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