Dipeptidyl peptidase IV, human, 10 MU

Dipeptidyl Peptidase Iv (Dpp-Iv) Human


Alcohol dehydrogenase

Alcohol Dehydrogenase


Phosphoglucose isomerase

Phosphoglucose Isomerase


Streptokinase catalyzes hydrolysis of amide linkages. Forms a 1:1 complex with plasminogen which is then converted to streptokinase-plasmin. Both streptokinase-plasminogen and streptokinase-plasmin complexes can activate plasminogen. As a result of its interaction with human or rabbit plasminogen, streptokinase undergoes specific fragmentation.

Pancreatin, USP

Pancreatin, U.S.P.





Beta-glucuronidases are members of the glycosidase family of enzymes that catalyze breakdown of complex carbohydrates. Human β-glucuronidase is a type of glucuronidase that catalyzes hydrolysis of β-D-glucuronic acid residues from the non-reducing end of mucopolysaccharides such as heparan sulfate. In human gut β-glucuronidase converts conjugated bilirubin to the unconjugated form for reabsorption.

Trypsin 1-250, virus free

Trypsin 1-250, Virus Free

Carbonic anhydrase

Carbonic Anhydrase

Leucine aminopeptidase

Leucine Aminopeptidase

Glycerol-3-phosphate oxidase

Glycerol-3-Phosphate Oxidase

Alkaline phosphatase

Alkaline Phosphatase

Malate dehydrogenase

Malate Dehydrogenase


Superoxide dismutase, ≥3500 U/mg solid

Superoxide dismutases are enzymes that catalyze the dismutation of superoxide into oxygen and hydrogen peroxide. Thus, they are an important antioxidant defense in nearly all cells exposed to oxygen.Superoxide dismutases are a group of low molecular weight metalloproteins present in all aerobic cells of plants, animals and micro-organisms. They provide protection against damaging reactions with the superoxide radical anion (O2-) by catalyzing its disproportionation into oxygen and hydrogen peroxide.

Aldehyde dehydrogenase

Aldehyde Dehydrogenase

Alkaline phosphatase

Alkaline Phosphatase

Catalase, 1 mg/mL

Catalase occurs in almost all aerobically respiring organisms and serves to protect cells from the toxic effects of hydrogen peroxide.It promotes growth of cells including T-cells, B-cells, myeloid leukemia cells, melanoma cells, mastocytoma cells and normal and transformed fibroblast cells.Defects in catalase are the cause of acatalasemia,a metabolic disorder characterized by absence of catalase activity in red cells and is often associated with ulcerating oral lesions.

Proteinase K, >30 mAnson U/mg

A highly active stable endopeptidase with a broad spectrum of action was isolated by E. Merk's Darmstadt Biochemical Research Department in 1970 from a culture filtrate of the fungus, Tritirachium album Limber, suitable for both protein and nucleic acid isolation, it exhibits proteolytic activity on proteins, peptides, glycoproteins, amides and esters. Also active with nitroanilides of amino acids with protected amino groups, excluding arginine.

Pancreatin 4x, USP

Pancreatin is a mixture of digestive enzymes produced by the exocrine cells of the pancreas. It is composed of amylase, lipase and protease. The trypsin found in pancreatin works to hydrolyze proteins into oligopeptides; amylase hydrolyzes starches into oligosaccharides and the disaccharide maltose; and lipase hydrolyzes triglycerides into fatty acids and glycerols.

Ribonuclease A

Ribonuclease belongs to pancreatic ribonuclease family. RNase A is an endoribonuclease that attacks at the 3¢ phosphate of a pyrimidine nucleotide. The sequence of pG-pG-pC-pA-pG will be cleaved to give pG-pG-pCp and A-pG.

Alkaline phosphatase

Alkaline Phosphatase