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a thermostable Taq DNA polymerase purified from the Thermus aquaticus strain in accordance with the procedures developed by Kaledin (1,2,3) for the isolation of thermostable enzymes processing DNA polymerase activity from thermophilic bacteria.
The 1 kb DNA ladder is suitable for sizing linear double-stranded DNA fragments .
To demonstrate the mobility of the DNA fragments
The 100 bp DNA ladder is suitable for sizing linear double-stranded DNA fragments from 100 to 1000 bp.
The recommended amount of size marker to load on an agarose gel is 0.5-1 µg per lane (5-10 µl).
To demonstrate the mobility of the DNA fragments, 1 µg of marker were loaded onto a 1% agarose gel.
AccuTherm™ is a thermostable enzyme possessing 5'-3' DNA polymerase and 3'-5' proof reading exonuclea-se activities. t is isolated from the hyperthermophilic marine archae Pyrococcus furiosis (Pfu).
a novel thermostable DNA polymerase that dramatically improves incorporation of Biotin- and Digoxigenin-dUTP as compared to Taq DNA polymerase
BioThermPlus™ DNA Polymerase is designed for maximum PCR success. It is a blend of BioTherm™ DNA Polymerase and Accutherm™ DNA Polymerase which allows amplification of longer templates with greater success and higher yields than either enzyme component alone. Together with a optimized buffer BioThermPlus™ DNA Polymerase provides the highest success rate of any PCR enzyme or enzyme blend.
BioThermT™ is a modified BioTherm™ DNA Polymerase to facilitate incorporation of Biotin- and Digoxigenin-dUTP in DN
BioTherm™ Mix is a 2.5x concentrated reagent mix for PCR comprising BioTherm™ DNA polymerase(0.06 u/µl), 2.5x PCR-Buffer with 3.75 mM MgCl2 , 500 µM of each dNTP and stabilizers.
Contains all four dNTPs in a pre-mixed solution, ready for immediate use
dNTP Set, BioTherm™ DNA polymerase, KlenTherm™ DNA polymerase, Synergy™ DNA polymerase, TthPlus™ DNA polymerase, GeneScript™ reverse transcriptase
Ready-to-use dNTP solutions are available as tetrasodium salts for use in DNA polymerization reactions and all DNA labelling and sequencing processes.
purified from the Thermus aquaticus strain by several rounds of liquid chromatography.