AASS Antibody
- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- Dry Ice Shipment: No


AASS Antibody
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.NCBI Gene ID:
10157Swiss Prot:
Q9UDR5Host:
RabbitReactivity:
Human, Mouse, RatImmunogen:
Recombinant fusion protein containing a sequence corresponding to amino acids 180-400 of human AASS (NP_005754.2) .Clonality:
PolyclonalConjugation:
UnconjugatedType:
Primary AntibodiesField of Research:
Signal TransductionPurification:
Affinity purificationPositive Control:
293TConcentration:
Batch dependentBuffer:
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.Modification:
NoneShipping Conditions:
Blue IceStorage Conditions:
Store at -20˚ C. Avoid freeze / thaw cycles.Calculated Molecular Weight:
Observed: 102kDaFragment:
IgGApplications Notes:
WB: 1:500 - 1:2000Symbol:
AASSPositive Control 2:
Mouse kidneyPositive Control 3:
Mouse liverPositive Control 4:
Mouse heartPositive Control 5:
Mouse brainPositive Control 6:
Rat kidneyNCBI Official Name:
Alpha-aminoadipic semialdehyde synthase, mitochondrialNCBI Organism:
Homo sapiensOther Product Names:
Alpha-aminoadipic semialdehyde synthase, mitochondrial, LKR/SDH, Lysine ketoglutarate reductase, LKR, LOR, Saccharopine dehydrogenase, SDH, AASSTested Applications:
WBPhysical Properties:
Liquid
