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AASS rabbit pAb

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],

Product Specifications

Background

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]

Product Name Alternative

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

UniProt

Q9UDR5

Swiss Prot

Q9UDR5

Reactivity

Human; Rat; Mouse

Immunogen

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

Target

AASS

Clonality

Polyclonal

Source

Rabbit

Applications

WB; ELISA

Concentration

1 mg/ml

Dilution

Western Blot: 1/500 - 1/2000. ELISA: 1/10000. Not yet tested in other applications.

Buffer

-20°C/1 year

Molecular Weight

102kD

Storage Conditions

-20°C/1 year

Observed Molecular Weight

102kD

Fragment

IgG

Subcellular Location

Mitochondrion .

Other Product Names

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

Gene ID (Human)

10157

Available Sizes

Curated Selection

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