Anti-TAT Polyclonal Antibody, 100.0ul

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.

• Size: 100.0ul
• Molecular Weight: 50kDa
• Physical State: Liquid
• Storage: Store at -20℃. Avoid freeze/thaw cycles.
• Application: WB;IF;IHC
• Brand: Saint Michael
• Catalogue No.: K108923P-100.0ul

For laboratory research use only. Not for human or animal consumption, diagnostic or therapeutic use.