Proteins that have the ability to structurally alter macromolecules without being altered themselves. Useful for a variety of molecular biology procedures; products include DNA and RNA polymerases, phosphatases, kinases, nucleases, etc.
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Degrade proteins even in the presence of detergents with Proteinase K, a broad-range endolytic protease widely used for digestion of proteins in nucleic acid preparations.
SH-reagents, such as N-ethylmaleimide, 2-iodobenzoic Acid, Iodoacetic Acid and Chloromercuribenzoic Acid, Heavy Metals (especially Cu2-) and Acetaldehyde (at high concentrations)
Form
Lyophilized Powder
Product Type
Aldehyde Dehydrogenase
Molecular Weight (g/mol)
≈200000
Color
Off-White
pH
9
Concentration
≈5 U/mg Protein, ≥1 U/mg Solid
For Use With (Application)
Oxidizes a number of Aliphatic and Aromatic Aldehydes
For consistent performance in a variety of molecular biology applications that require animal-free formulations, high quality recombinant BSA can be used to stabilize enzymes, enhance enzymatic activity, or to block non-specific binding.
Klenow Fragment, exo- is the large fragment of DNA polymerase I. Exhibits 5'→3' polymerase activity, but lacks the 3'→5' and 5'→3' exonuclease activities.
OPTIZYME™ T4 DNA Pol Buffer 5X: Tris HCl 335mM (8.8 pH at 25°C), MgCl2 33mM, DTT 5mM, (NH4)2SO4 84mM
Color
Colorless
pH
7.5
Concentration
5 U/μL
For Use With (Application)
Synthesis of labeled DNA probes, creation of blunt PCR products with 3'-dA overhangs, ligation-independent cloning of PCR products, Restriction Enzymes, reverse transcriptases and T4 DNA ligase
Source
E. coli cells with a cloned gene 43 of bacteriophage T4
Thermo Scientific TheraPure in vitro transcription (IVT) enzymes are designed for advanced research and early development of mRNA therapeutics and vaccines.