Background:

AASS 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.

Classification:

Primary antibody

Alternative names:

AASS; Alpha-aminoadipic semialdehyde synthase; mitochondrial; LKR/SDH

Species reactivity:

Human

Host:

Rabbit

Isotype:

IgG

Immunogen:

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

Concentration:

1 mg/ml

Molecular weight:

102132

Applications:

WB, ELISA

Storage:

-20°C for one year

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