AASS Antilichaam

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.

10157

Q9UDR5

Human, Mouse, Rat

Recombinant fusion protein containing a sequence corresponding to amino acids 180-400 of human AASS (NP_005754.2) .

Unconjugated

Primary Antibodies

Signal Transduction

Affinity purification

293T

Batch dependent

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

None

Blue Ice

Store at -20˚ C. Avoid freeze / thaw cycles.

Observed: 102kDa

IgG

WB: 1:500 - 1:2000

AASS

Mouse kidney

Mouse liver

Mouse heart

Mouse brain

Rat kidney

Alpha-aminoadipic semialdehyde synthase, mitochondrial

Homo sapiens

Alpha-aminoadipic semialdehyde synthase, mitochondrial, LKR/SDH, Lysine ketoglutarate reductase, LKR, LOR, Saccharopine dehydrogenase, SDH, AASS

WB

Liquid