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首页 > 产品中心 > 抗体系列 > 一抗

货号:BSCY0274

CD36 Rabbit mAb

CD36;GP3B;GP4;Platelet glycoprotein 4;Fatty acid translocase;FAT;Glycoprotein IIIb;GPIIIB;Leukocyte differentiation antigen CD36;PAS IV;PAS-4;Platelet collagen receptor;Platelet glycoprotein IV;GPIV;Thrombospondin receptor;CD36

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别名 CD36;GP3B;GP4;Platelet glycoprotein 4;Fatty acid translocase;FAT;Glycoprotein IIIb;GPIIIB;Leukocyte differentiation antigen CD36;PAS IV;PAS-4;Platelet collagen receptor;Platelet glycoprotein IV;GPIV;Thrombospondin receptor;CD36
基因名称 CD36
蛋白名称 Platelet glycoprotein 4
推荐应用
反应物种 Human,Mouse,Rat,
存储缓冲液 PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
Human Gene Link 948
Human Swissprot No. P16671
Mouse Gene ID 12491
Mouse Swissprot No. Q08857
Rat Swissprot No. Q07969
特异性 endogenous
稀释度 IHC 1:1000-1:4000;WB 1:1000-1:2500;IF 1:200-1:1000;ELISA 1:5000-1:20000;IP 1:50-1:200;
参考分子量 MW(Observed):90kD
预测分子量 MW(Calculated):53kD
运输及保存条件 -15°C to -25°C/1 year(Do not lower than -25°C)
宿主 Rabbit
同种型 IgG,Kappa
背景介绍 The protein encoded by this gene is the fourth major glycoprotein of the platelet surface and serves as a receptor for thrombospondin in platelets and various cell lines. Since thrombospondins are widely distributed proteins involved in a variety of adhesive processes, this protein may have important functions as a cell adhesion molecule. It binds to collagen, thrombospondin, anionic phospholipids and oxidized LDL. It directly mediates cytoadherence of Plasmodium falciparum parasitized erythrocytes and it binds long chain fatty acids and may function in the transport and/or as a regulator of fatty acid transport. Mutations in this gene cause platelet glycoprotein deficiency. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Feb 2014],
细胞定位 Membrane
功能 Disease:Defects in CD36 are the cause of platelet glycoprotein IV deficiency [MIM:608404]; also known as CD36 deficiency. Platelet glycoprotein IV deficiency can be divided into 2 subgroups. The type I phenotype is characterized by platelets and monocytes/macrophages exhibiting complete CD36 deficiency. The type II phenotype lacks the surface expression of CD36 in platelets, but expression in monocytes/macrophages is near normal.,Disease:Genetic variations in CD36 are associated with susceptibility to coronary heart disease type 7 (CHDS7) [MIM:610938].,Function:Seems to have numerous potential physiological functions. Binds to collagen, thrombospondin, anionic phospholipids and oxidized LDL. May function as a cell adhesion molecule. Directly mediates cytoadherence of Plasmodium falciparum parasitized erythrocytes. Binds long chain fatty acids and may function in the transport and/or as a regulator of fatty acid transport.,online information:CD36 entry,polymorphism:Genetic variation in CD36 influences the severity and outcome of malaria infection.,PTM:N-glycosylated and O-glycosylated with a ratio of 2:1.,similarity:Belongs to the CD36 family.,
纯化 Protein A
Clonality Monoclonal
修饰类型 Unmodified
细胞定位 Membrane
组织表达 Adipocyte,Liver,Mammary gland,Milk,Placenta,Platelet,Skeletal muscle,
研究领域 >>PPAR signaling pathway;>>Phagosome;>>AMPK signaling pathway;>>ECM-receptor interaction;>>Hematopoietic cell lineage;>>Adipocytokine signaling pathway;>>Insulin resistance;>>Fat digestion and absorption;>>Cholesterol metabolism;>>Malaria;>>Diabetic cardiomyopathy;>>Lipid and atherosclerosis

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