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Invitrogen™ GNPAT Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA5101555
Description
Antibody detects endogenous levels of total GNPAT.
GNPAT is a key enzyme located in the peroxisomal membrane which is essential to the synthesis of ether phospholipids. Mutations in GNPAT are associated with rhizomelic chondrodysplasia punctata type 2, which is characterized by rhizomelic shortening of femur and humerus, vertebral disorders, cataract, cutaneous lesions and severe mental retardation.
Specifications
GNPAT | |
Polyclonal | |
Unconjugated | |
GNPAT | |
acyl-CoA:dihydroxyacetonephosphate acyltransferase; acyl-CoA:dihydroxyacetonephosphateacyltransferase; AU019525; D1Ertd819e; DAPAT; DAP-AT; DHAPAT; DHAP-AT; Dihydroxyacetone phosphate acyltransferase; glycerone-phosphate O-acyltransferase; glyceronephosphate O-acyltransferase; GNPAT; RCDP2 | |
Rabbit | |
Affinity chromatography | |
RUO | |
8443 | |
-20°C | |
Liquid |
Western Blot, Immunocytochemistry | |
1 mg/mL | |
PBS with 50% glycerol and 0.02% sodium azide; pH 7.4 | |
O15228 | |
GNPAT | |
A synthesized peptide derived from human GNPAT(Accession O15228), corresponding to amino acid residues V332-V382. | |
100 μL | |
Primary | |
Human | |
Antibody | |
IgG |
Safety and Handling
WARNING: Cancer - www.P65Warnings.ca.gov
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