Background:

This nuclear gene TAT (tyrosine aminotransferase) encodes a mitochondrial protein tyrosine aminotransferase which is present in the liver and catalyzes the conversion of L-tyrosine into p-hydroxyphenylpyruvate. Mutations in TAT 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.

Classification:

Primary antibody

Alternative names:

TAT; Tyrosine aminotransferase; TAT; L-tyrosine:2-oxoglutarate aminotransferase

Species reactivity:

Human;Mouse;Rat

Host:

Rabbit

Isotype:

IgG

Immunogen:

The antiserum was produced against synthesized peptide derived from human TAT. AA range:255-304

Concentration:

1 mg/ml

Molecular weight:

50399

Applications:

IHC-p, ELISA

Storage:

-20°C for one year

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