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Invitrogen™ GNPAT Polyclonal Antibody

Rabbit Polyclonal Antibody

Supplier:  Invitrogen™ PA5101555

Catalog No. PIPA5101555


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Description

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.
TRUSTED_SUSTAINABILITY
Specifications

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
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