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GNPAT Rabbit anti-Human, Polyclonal, Invitrogen™
Rabbit Polyclonal Antibody
Supplier: Thermo Scientific PA572492
Description
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 | |
Dihydroxyacetone phosphate acyltransferase; DAP-AT; DHAP-AT; Acyl-CoA:dihydroxyacetonephosphateacyltransferase; Glycerone-phosphate O-acyltransferase; GNPAT; DAPAT; DHAPAT | |
Rabbit | |
Protein A | |
RUO | |
8443 | |
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. | |
Liquid |
Flow Cytometry, Immunohistochemistry (Paraffin), Western Blot | |
0.46 mg/mL | |
PBS with 0.09% sodium azide | |
O15228 | |
GNPAT | |
KLH conjugated synthetic peptide between 654-680 amino acids from the C-terminal region of human GNPAT | |
400 μL | |
Primary | |
Human | |
Antibody | |
IgG |
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