Human Tyrosine Aminotransferase protein, His tag

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 cognitive disability. A regulator gene for tyrosine aminotransferase is X-linked. [provided by RefSeq, Jul 28]
Read more
€0.00 (tax incl.)
Reference:
GTX00184-pro
Brand:
Product Details
GTX00184-pro

Data sheet

Size
10μg
Conjugation
Unconjugated
Application
Functional Assay
URL - Product
https://www.genetex.com/Product/Detail/Human-Tyrosine-Aminotransferase-protein-His-tag/GTX00184-pro

Menu

Settings