TAT Polyclonal Antibody, 50ul Hybridoma Antibody Sequencing The second intron contains an

The second intron contains an apparently intronless gene

The encoded protein aids in translation initiation by recruiting ribosomes to the 5'-cap structure

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 re-sealable bag ensures long-lasting use

TAT Polyclonal Antibody, 50ul Hybridoma Antibody Sequencing The second intron contains anThis 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.