Standard PCR Reagents

Useful for a range of PCR operations, Moltaq plays a crucial role in amplification of DNA for many applications. As an example,  in Single-nucleotide polymorphism, Moltaq sees uses for quality measurement of food and water, for gene mutation research, and many others.

A variety of kits are available depending on your need. These kits will meet your needs for high performance PCR amplification in daily routine. MolTaq is the standard Taq DNA polymerase kit supplying PCR buffer (1.5mM MgSO4) and PCR enhancer for high G+C content targets.

MolTaq Basic enables optimization of PCR amplification by variation of Mg2+ concentration (basic buffer and extra 100 mM MgCl2 solution). Control of accurate pipetting and direct transfer of the amplification reaction to the gel for analysis is possible using MolTaqRED and MolTaqRED basic, respectively.

Catalog Numbers

Catalog #
Test Description

P-010-1000

P-010-5000

P-016-1000

P-016-5000

P-017-1000

P-017-5000

P-040-1000

P-040-5000

P-060-1000

P-060-5000

MolTaq – Thermostable DNA Polymerase (1000 Reactions)

MolTaq – Thermostable DNA Polymerase (5000 Reactions)

MolTaq Basic – Thermostable DNA Polymerase ¹ (1000 Reactions)

MolTaq Basic – Thermostable DNA Polymerase¹ (1000 Reactions)

Hot MolTaq – Hot start Thermostable DNA Polymerase (1000 Reactions)

Hot MolTaq – Hot start Thermostable DNA Polymerase (1000 Reactions)

MolTaq Red – Basic Thermostable DNA Polymerase¹ (1000 Reactions)

MolTaq Red – Basic Thermostable DNA Polymerase¹ (1000 Reactions)

Hot MolTaq – Basic Hot start thermostable DNA Polymerase (1000 Reactions)

Hot MolTaq – Basic Hot start thermostable DNA Polymerase (1000 Reactions)

¹: Mg(2+) supplied separately

²: Red dye for visualization

Publications

Effect of seaweed-derived laminarin and fucoidan and zinc oxide on gut morphology, nutrient transporters, nutrient digestibility, growth performance and selected microbial populations in weaned pigs (Heim G, 2014)

(Cryptic) sex in the microsporidian Nosema granulosis – evidence from parasite rDNA and host mitochondrial DNA (Krebes L, 2014)

Autophagic kinases SmVPS34 and SmVPS15 are required for viability in the filamentous ascomycete Sordaria macrospora (Voigt O, 2014)

Mutational modifications of hepatitis A virus proteins 2B and 2C described for cell culture-adapted and attenuated virus are present in wild-type virus populations (Weilandt R, 2014)

Evolutionary systematics of the Australian Eocyzicus fauna (Crustacea: Branchiopoda: Spinicaudata) reveals hidden diversity and phylogeographic structure (Schwentner M, 2013)

Prevalence of clinically relevant antibiotic resistance genes in surface water samples collected from Germany and Australia (Stoll C, 2012)

Phenotypic variability in RDH5 retinopathy (Fundus Albipunctatus) (Sergouniotis P, 2011)

Composition of epiphytic bacterial communities differs on petals and leaves (Junker R, 2011)

A Survey of DNA Variation of C2ORF71 in Probands with Progressive Autosomal Recessive Retinal Degeneration and Control (Sergouniotis P, 2011)

Estimation of dispersal distances of the obligately plant-associated ant Crematogaster decamera (Turke M, 2010)

Small, specialised and highly mobile? The tree-hole breeding frog, Phrynobatrachus guineensis, lacks fine-scale population structure (Sandberger-Loua L. 2010)

Dok-7 promotes slow muscle integrity as well as neuromuscular junction formation in a zebrafish model of congenital myasthenic syndromes (Müller J, 2010)

A detailed phenotypic assessment of individuals affected by MFRP-related oculopathy (Mukhopadhyay B, 2010)

Novel mutations in MERTK associated with childhood onset rodcone dystrophy (Mackay D, 2010)

Glacial-driven vicariance in the amphipod Gammarus duebeni (Krebes L, 2010)

Glucose and glucose 6-phosphate as carbon sources in extra- and intracellular growth of enteroinvasive Escherichia coli and Salmonella enterica (Götz A, 2010)

Detection of Toxoplasma gondii, Neospora caninum, and Encephalitozoon cuniculi in the brains of common voles (Microtus arvalis) and water voles (Arvicola terrestris) by gene amplification techniques in western Austria (Fuehrer H, 2010)

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