|Western Blot (WB)||1:500-1:1000|
|Tested Species reactivity||Human|
|Host / Isotype||Rabbit / IgG|
|Immunogen||A synthetic peptide derived from the C-terminal region of human GNPAT|
|Purification||Antigen affinity chromatography|
|Storage buffer||Dulbecco's PBS, pH 7.4, with 50% glycerol, 150mM NaCl|
|Contains||0.02% sodium azide|
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Acyl-CoA:dihydroxyacetonephosphateacyltransferase; DAP-AT; DAPAT; DHAP-AT; DHAPAT; Dihydroxyacetone phosphate acyltransferase; Glycerone-phosphate O-acyltransferase; GNPAT
Gene Aliases: DAP-AT; DAPAT; DHAPAT; GNPAT; RCDP2
UniProt ID: (Human) O15228
Entrez Gene ID: (Human) 8443
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