TAT Polyclonal Antibody, 50ul Hybridoma Antibody Sequencing Alterations in the subunit composition

Alterations in the subunit composition of the receptor are associated with pathophysiological conditions such as Parkinson's disease

Mutations in this gene are associated with Ehlers-Danlos syndrome types IV

The encoded preproprotein is proteolytically processed by plasmin or trypsin to generate heavy and light chains

60S ribosomal protein L17 belongs to the L22P family of ribosomal proteins

TAT Polyclonal Antibody, 50ul Hybridoma Antibody Sequencing Alterations in the subunit compositionThis 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.