Esta buscando: 4-Hydroxyphenylpyruvic+acid

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4-Hydroxyphenylpyruvic acid ≥95.0% (by HPLC, titration analysis)

Proveedor: TCI

Descripción: 4-Hydroxyphenylpyruvic acid ≥95.0% (by HPLC, titration analysis)

4-Hydroxyphenylpyruvic acid 95%

Proveedor: Apollo Scientific

Descripción: 4-Hydroxyphenylpyruvic acid 95%

Anti-HPD Mouse Monoclonal Antibody [clone: 2F3]

Numero del catalogo: (USBI128056)

Proveedor: US Biological

Descripción: Anti-HPD Mouse Monoclonal Antibody [clone: 2F3]

UOM: 1 * 100 µG

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Human recombinant 4HPPD (from E. coli)

Numero del catalogo: (PRSI92-016)

Proveedor: ProSci Inc.

Descripción: 4-Hydroxyphenylpyruvate Dioxygenase (4HPPD) belongs to the 4HPPD family. 4HPPD is a key enzyme in the degradation of tyrosine, which catalyzes the second reaction in the catabolism of tyrosine the conversation of 4-hydroxyphenylpyruvate to homogentisate. 4HPPD exists in homodimer forms, which uses zinc as a cofactor to catalyze the third step in the conversion of L-phenylalanine to fumarate and acetoacetic acid. When the active 4HPPD enzyme concentration is low in the human body, it results in high levels of tyrosine concentration in the blood, which can cause mild mental retardation at birth, and degradation in vision as a patient grows older.

UOM: 1 * 50 µG

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N/A Each

Anti-TAT Rabbit Polyclonal Antibody

Numero del catalogo: (BOSSBS-1907R)

Proveedor: Bioss

Descripción: This nuclear gene encodes a mitochondrial protein tyrosine aminotransferase which is present in the liver and catalyzes the conversion of L-tyrosine into p-hydroxyphenylpyruvate. Mutations in this gene cause tyrosinemia (type II, Richner-Hanhart syndrome), a disorder accompanied by major skin and corneal lesions, with possible mental retardation. A regulator gene for tyrosine aminotransferase is X-linked.

UOM: 1 * 100 µl

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