
Enzymes, or biological catalysts, are some of the most widely manipulated reagents in molecular biology and biochemistry research and diagnostics. The appropriate enzymatic reagent depends on the type of enzyme, target molecule, final reaction product, reagent grade, and working volume. Peptidases, enzymes that initiate protein catabolism by hydrolysis of the peptide bonds that link amino acids together in the polypeptide chain, DNA glycosylases, the enzymes involved in base excision repair, and kinases, enzymes that transfers phosphate groups from high-energy donor molecules, such as ATP to specific substrates, are examples of available enzymes from suppliers such as New England Biolabs®, Promega, and Roche. DNA experiments use nucleic acid-specific enzymes, such as restriction enzymes which cut DNA, ligases which join DNA bases, and topoisomerases which uncoil DNA. If a simple protein detection scheme is the target, the available selection of HRP (Horseradish Peroxidase) products will complement any experimental design. Enzymes are synthesized in various quantities, so researchers have the option of 100µg or 100g of Trypsin, for example. Catalyze your research goals with the products in this enzyme collection.
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Introducing the LUNA-FX7™ - the automated cell counter that builds on the success of its predecessors. The LUNA-FX7™ is our most powerful cell counter to date, with unmatched cell counting accuracy, a maximum counting volume of 5 µL (10 times that of...
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Measure and assess your cell cultures with ease. Our Millicell® DCI Digital Cell Imager enables more efficient execution of the repetitive daily techniques associated with cell passaging. Quickly and objectively assess confluency, morphology, ...
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I used Thermo Scientific RNase A to degrade unprotected mRNA during a gel retention assay to evaluate the protective effect of lipid nanoparticles (LNPs). Using 1 µL RNase A provided efficient RNA digestion while allowing clear discrimination between...
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I work extensively with cell wall hydrolases (enzymes) of bacteria. To check the enzymatic activity, I have to solubilize the intact cell wall of bacteria using mutanolysin. To examine the specific site of action on the cell wall, the resultant ...
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