Descrizione Azione

A synthesized peptide derived from human Tyrosinase, corresponding to a region within C-terminal amino acids.

Codice: DF6383 Confezionamento: 100ul
Dettagli

A synthetic peptide from human Tyrosinase

Codice: BF3336 Confezionamento: 100ul
Dettagli

A synthesized peptide derived from human Tyrosine Hydroxylase, corresponding to a region within N-terminal amino acids.

Codice: AF6113 Confezionamento: 100ul
Dettagli

A synthesized peptide derived from human TyrHydroxylase around the site of Ser40.

Codice: BF8114 Confezionamento: 100ul
Dettagli

TH (Tyrosine 3-hydroxylase), also known as Tyrosine 3-monooxygenase, is a 60-62 kDa member of the biopterin-dependent aromatic amino acid hydroxylase family of molecules. It is expressed by neurons of the dopamine and autonomic nervous system, plus the neuroendocrine cells of the adrenal medulla. TH is considered the rate limiting enzyme for catecholamine synthesis, and serves to catalyze the hydroxylation of L-tyrosine.

Codice: E-AB-40585_100μL Confezionamento: 100μL
Dettagli

TH (Tyrosine 3-hydroxylase), also known as Tyrosine 3-monooxygenase, is a 60-62 kDa member of the biopterin-dependent aromatic amino acid hydroxylase family of molecules. It is expressed by neurons of the dopamine and autonomic nervous system, plus the neuroendocrine cells of the adrenal medulla. TH is considered the rate limiting enzyme for catecholamine synthesis, and serves to catalyze the hydroxylation of L-tyrosine.

Codice: E-AB-40585_25μL Confezionamento: 25μL
Dettagli

A synthetic peptide from human Tyrosine Hydroxylase

Codice: BF3158 Confezionamento: 100ul
Dettagli

The enzyme encoded by this gene catalyzes the first 2 steps, and at least 1 subsequent step, in the conversion of tyrosine to melanin. The enzyme has both tyrosine hydroxylase and dopa oxidase catalytic activities, and requires copper for function. Mutations in this gene result in oculocutaneous albinism, and nonpathologic polymorphisms result in skin pigmentation variation. The human genome contains a pseudogene similar to the 3' half of this gene.

Codice: E-AB-14431_120μL Confezionamento: 120μL
Dettagli

The enzyme encoded by this gene catalyzes the first 2 steps, and at least 1 subsequent step, in the conversion of tyrosine to melanin. The enzyme has both tyrosine hydroxylase and dopa oxidase catalytic activities, and requires copper for function. Mutations in this gene result in oculocutaneous albinism, and nonpathologic polymorphisms result in skin pigmentation variation. The human genome contains a pseudogene similar to the 3' half of this gene.

Codice: E-AB-14431_20μL Confezionamento: 20μL
Dettagli

The enzyme encoded by this gene catalyzes the first 2 steps, and at least 1 subsequent step, in the conversion of tyrosine to melanin. The enzyme has both tyrosine hydroxylase and dopa oxidase catalytic activities, and requires copper for function. Mutations in this gene result in oculocutaneous albinism, and nonpathologic polymorphisms result in skin pigmentation variation. The human genome contains a pseudogene similar to the 3' half of this gene.

Codice: E-AB-14431_200μL Confezionamento: 200μL
Dettagli

The enzyme encoded by this gene catalyzes the first 2 steps, and at least 1 subsequent step, in the conversion of tyrosine to melanin. The enzyme has both tyrosine hydroxylase and dopa oxidase catalytic activities, and requires copper for function. Mutations in this gene result in oculocutaneous albinism, and nonpathologic polymorphisms result in skin pigmentation variation. The human genome contains a pseudogene similar to the 3' half of this gene.

Codice: E-AB-14431_60μL Confezionamento: 60μL
Dettagli

A synthesized peptide derived from Human U1A.

Codice: DF13997 Confezionamento: 100ul
Dettagli