AAT Polyclonal Antibody, 50ul[BT-AP00075] Culture Media Two transcript variants encoding the

Two transcript variants encoding the same pr

it's perfect for your cell culture needs

Mutations in this gene cause Leber congenital amaurosis type 12| a disease that results in retinal degeneration

The recombination activating gene 1 component is thought to contain most of the catalytic activity

AAT Polyclonal Antibody, 50ul[BT-AP00075] Culture Media Two transcript variants encoding theAASS encodes a bifunctional enzyme (aminoadipate semialdehyde synthase) that catalyzes the first two steps in the mammalian lysine degradation pathway. The N terminal and the C terminal portions of this enzyme contain lysine ketoglutarate reductase and saccharopine dehydrogenase activity, respectively, resulting in the conversion of lysine to alpha aminoadipic semialdehyde. Mutations in AASS are associated with familial hyperlysinemia.