Enzyme Activators

Butyl butyrate is an ester present in pineapple flavor and is very important for the food and beverages industries . Kinetcis of butyl butyrate synthesis by enzymatic esterification and trans -esterification in supercritical carbon dioxide with a

Research area: Cell Signaling Catalase is an active enzyme present in aerobic organisms. It is a ferric hemoprotein and a tetramer.

Research area: Cell Signaling Catalase is an active enzyme present in aerobic organisms. It is a ferric hemoprotein and a tetramer.

Application Catalase acts as a natural antioxidant to study the roles of reactive oxygen species in gene expression and apoptosis. It has also been used to protect against oxidative damage to proteins, lipids, and nucleic acids.

Application Catalase acts as a natural antioxidant to study the roles of reactive oxygen species in gene expression and apoptosis. It has also been used to protect against oxidative damage to proteins, lipids, and nucleic acids.

Application Catalase acts as a natural antioxidant to study the roles of reactive oxygen species in gene expression and apoptosis. It has also been used to protect against oxidative damage to proteins, lipids, and nucleic acids.

Application Catalase acts as a natural antioxidant to study the roles of reactive oxygen species in gene expression and apoptosis. It has also been used to protect against oxidative damage to proteins, lipids, and nucleic acids.

Application Catalase acts as a natural antioxidant to study the roles of reactive oxygen species in gene expression and apoptosis. It has also been used to protect against oxidative damage to proteins, lipids, and nucleic acids.

Cellubiohydrolase I is an enzyme present in many fungi, but particularly wood rot fungi. It is a monomer of 53 kDa with a catalytic domain and a cellulose binding domain.

Biochem/physiol Actions Acyl group acceptor Substrates Choline acetyltransferase substrate

1 unit is defined as the amount of enzyme required to achieve the maximum site-specific recombination of 250ng of control DNA in 30 minutes at 37℃ in a 50μl reaction system. The maximum recombination can be analyzed by agarose gel electrophoresis or

1 unit is defined as the amount of enzyme required to achieve the maximum site-specific recombination of 250ng of control DNA in 30 minutes at 37℃ in a 50μl reaction system. The maximum recombination can be analyzed by agarose gel electrophoresis or