AASS Polyclonal Antibody

Background:
aminoadipate-semialdehyde synthase(AASS) Homo sapiens This gene encodes a bifunctional enzyme 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 this gene are associated with familial hyperlysinemia. [provided by RefSeq, Jul 2008],

Alternative Names:
AASS, Alpha-aminoadipic semialdehyde synthase, mitochondrial, LKR/SDH

Immunogen: The antiserum was produced against synthesized peptide derived from human AASS. AA range:251-300

Isotype: Rabbit

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Concentration: 1 mg/ml

Observed band: 102

GeneID: AASS

Storage: -20°C/1 year

NOTE: For Research Use Only