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GNPAT Polyclonal Antibody
GNPAT Polyclonal Antibody
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GNPAT Polyclonal Antibody
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经销商客户: ¥440.0
实验室客户: ¥600.0
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商品描述

商品属性

Target:GNPAT

Fields:Glycerophospholipid metabolism;Peroxisome

Gene Name:GNPAT

Protein Name:Dihydroxyacetone phosphate acyltransferase

Human Gene Id:8443

Human Swiss Prot No:O15228

Mouse Swiss Prot No:P98192

Immunogen:The antiserum was produced against synthesized peptide derived from human GNPAT. AA range:231-280

Specificity:GNPAT Polyclonal Antibody detects endogenous levels of GNPAT protein.

Formulation:Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

Source:Polyclonal, Rabbit,IgG

Dilution:WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:20000.. IF 1:50-200

Purification:The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Concentration:1 mg/ml

Storage Stability:-15°C to -25°C/1 year(Do not lower than -25°C)

Other Name:GNPAT;DAPAT;DHAPAT;Dihydroxyacetone phosphate acyltransferase;DAP-AT;DHAP-AT;Acyl-CoA:dihydroxyacetonephosphateacyltransferase;Glycerone-phosphate O-acyltransferase

Observed Band(KD):77kD

Background: This gene encodes an enzyme located in the peroxisomal membrane which is essential to the synthesis of ether phospholipids. Mutations in this gene are associated with rhizomelic chondrodysplasia punctata. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015],

Function:catalytic activity:Acyl-CoA + glycerone phosphate = CoA + acylglycerone phosphate.,disease:Defects in GNPAT are the cause of rhizomelic chondrodysplasia punctata type 2 (RCDP2) [MIM:222765]. RDCP2 is characterized by rhizomelic shortening of femur and humerus, vertebral disorders, cataract, cutaneous lesions and severe mental retardation.,domain:The HXXXXD motif is essential for acyltransferase activity and may constitute the binding site for the phosphate moiety of the glycerol-3-phosphate.,pathway:Membrane lipid metabolism; glycerophospholipid metabolism.,similarity:Belongs to the GPAT/DAPAT family.,subcellular location:Exclusively localized to the lumenal side of the peroxisomal membrane.,subunit:May be part of an heterotrimeric complex composed of DAP-AT, ADAP-S and a modified form of DAP-AT.,

Subcellular Location:Peroxisome membrane ; Peripheral membrane protein ; Matrix side . Exclusively localized to the lumenal side of the peroxisomal membrane. .

Expression: Aorta endothelial cell,Brain,Liver,Lung,Thymus,

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