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首页 > 产品中心 > 抗体系列 > 一抗

货号:BSCY30292

CD63 Rabbit mAb

CD63, MLA1, TSPAN30, CD63 antigen, Granulophysin, Lysosomal-associated membrane protein 3, Lysosome integral membrane protein 1, Melanoma-associated antigen ME491, OMA81H, Ocular melanoma-associated antigen, Tetraspanin-30, LAMP-3, Limp1, Tspan-30

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别名 CD63, MLA1, TSPAN30, CD63 antigen, Granulophysin, Lysosomal-associated membrane protein 3, Lysosome integral membrane protein 1, Melanoma-associated antigen ME491, OMA81H, Ocular melanoma-associated antigen, Tetraspanin-30, LAMP-3, Limp1, Tspan-30
基因名称 CD63 MLA1 TSPAN30
蛋白名称 CD63 antigen (Granulophysin) (Lysosomal-associated membrane protein 3) (LAMP-3) (Lysosome integral membrane protein 1) (Limp1) (Melanoma-associated antigen ME491) (OMA81H) (Ocular melanoma-associated antigen) (Tetraspanin-30) (Tspan-30) (CD antigen CD63)
推荐应用
反应物种 Human
存储缓冲液 PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
Human Swissprot No. P08962
特异性 Endogenous
稀释度 IHC 1:100-1:300
预测分子量 26kDa
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 a member of the transmembrane 4 superfamily , also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development , activation , growth and motility. The encoded protein is a cell surface glycoprotein that is known to complex with integrins. It may function as a blood platelet activation marker. Deficiency of this protein is associated with Hermansky-Pudlak syndrome. Also this gene has been associated with tumor progression. Alternative splicing results in multiple transcript variants encoding different protein isoforms.
细胞定位 Membrane, Lysosome
功能 Function:This antigen is associated with early stages of melanoma tumor progression. May play a role in growth regulation. ,miscellaneous:Lack of expression of CD63 in platelets has been observed in a patient with Hermansky-Pudlak syndrome (HPS) . Hermansky-Pudlak syndrome (HPS) is a genetically heterogeneous , rare , autosomal recessive disorder characterized by oculocutaneous albinism , bleeding due to platelet storage pool deficiency , and lysosomal storage defects. This syndrome results from defects of diverse cytoplasmic organelles including melanosomes , platelet dense granules and lysosomes. Ceroid storage in the lungs is associated with pulmonary fibrosis , a common cause of premature death in individuals with HPS.
纯化 Protein A
Clonality Monoclonal
修饰类型 Unmodified
细胞定位 Membrane, Lysosome
组织表达 Ubiquitous expression

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