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


AGPS Polyclonal Antibody
Background :
AGPS is a 658 amino acid enzyme that is required for glycerolipid metabolism and ether lipid biosynthesis. Localized to the inner aspect of the peroxisomal membrane, AGPS is likely part of a heterotrimeric complex that is also composed of GNPAT and a modified form of GNPAT. Containing one FAD-binding PCMH-type domain, AGPS utilizes FAD as a cofactor in the synthesis of alkyl-glycerone 3-phophate and a long-chain acid anion from 1-acteyl-glyerone 3-phosphate and a long-chain alcohol. Defects in the gene encoding AGPS results in rhizomelic chondrodysplasia punctata type 3, a disease characterized by vertebral disorders, severe mental retardation, cutaneous lesions, cataracts and rhizomelic shortening of the humerus and femur.Synonyms :
AAG5; ADAP-S; ADAS; ADAS_HUMAN; ADHAPS; ADPS; Aging associated gene 5 protein; Aging-associated gene 5 protein; AGPS; ALDHPSY; Alkyl-DHAP synthase; Alkyldihydroxyacetonephosphate synthase; Alkyldihydroxyacetonephosphate synthase, peroxisomal; Alkylglycerone phosphate synthase; Alkylglycerone-phosphate synthase; peroxisomal.Gene ID :
8540Cellular Locus :
Cytoplasm, Cell membraneHost :
RabbitCross Reactivity :
RatImmunogen :
31-130/658Target :
AGPSClonality :
PolyclonalIsotype :
IgGConjugation :
UnconjugatedSource :
KLH conjugated synthetic peptide derived from human AGPS/Alkyl-DHAP synthaseApplications :
ELISA, IHC-P, IHC-F, IF (IHC-P), IF (IHC-F), IF (ICC)Purification :
Purified by Protein A.Concentration :
1µg/µlDilution :
ELISA (1:500-1000), IHC-P (1:200-400), IHC-F (1:100-500), IF (IHC-P) (1:50-200), IF (IHC-F) (1:50-200), IF (ICC) (1:50-200)Buffer :
0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.Modification :
UnmodifiedStorage Conditions :
Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.Gene ID URL :
8540Predicted Cross Reactivity :
Human, Mouse, Cow, Pig, Horse

