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TMEM15/跨膜蛋白15抗体

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产品名称: TMEM15/跨膜蛋白15抗体
产品型号: DOLK
产品展商: 单克隆抗体/多克隆抗体
产品文档: 无相关文档

简单介绍

TMEM15/跨膜蛋白15抗体应用于IHC、WB、 IF、IP、ELISA等科研实验,按理化性质和生物学功能IgM、IgG、IgA、IgE、IgD五类。按抗体的来源,可将其分为天然抗体和**抗体。TMEM15/跨膜蛋白15抗体生产每个流程都执行严格的检测标准,保证蛋白抗原产品质量,质量稳定,实验效果明显。


TMEM15/跨膜蛋白15抗体  的详细介绍

TMEM15/跨膜蛋白15抗体

规格:1mg/1ml

英文名: DOLK

别名: CDG1M; DK; DK1; Dolichol kinase; KIAA1094; DOLK_HUMAN; SEC59; SEC59, YEAST, HOMOLOG OF; TMEM15; Transmembrane protein 15.

分子量: 59kDa

储存液:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce

克隆类型:Polyclonal

亚型:IgG

纯化方法:affinity purified by Protein A

**原:KLH conjugated synthetic peptide derived from human DOLK

交叉反应:Human, Mouse, Rat, Chicken, Pig, Cow, Horse, Sheep,

细胞定位:细胞膜

TMEM15/跨膜蛋白15抗体产品介绍:background: The protein encoded by this gene catalyzes the CTP-mediated phosphorylation of dolichol, and is involved in the synthesis of Dol-P-Man, which is an essential glycosyl carrier lipid for C- and O-mannosylation, N- and O-linked glycosylation of proteins, and for the biosynthesis of glycosyl phosphatidylinositol anchors in endoplasmic reticulum. Mutations in this gene are associated with dolichol kinase deficiency.[provided by RefSeq, Apr 2010] Function: DOLK belongs to the polyprenol kinase family. Defects inTMEM15/跨膜蛋白15抗体 DOLK are the cause of congenital disorder of glycosylation type 1M (CDG1M), also known as dolichol kinase deficiency. Subcellular Location: Endoplasmic reticulum integral membrane protein Tissue Specificity: Ubiquitous. DISEASE: Congenital disorder of glycosylation 1M (CDG1M) [MIM:610768]: A multisystem disorder caused by a defect in glycoprotein biosynthesis and characterized by under-glycosylated TMEM15/跨膜蛋白15抗体serum glycoproteins. Congenital disorders of glycosylation result in a wide variety of clinical features, such as defects in the nervous system development, psychomotor retardation, dysmorphic features, hypotonia, coagulation disorders, and immunodeficiency. The broad spectrum of features reflects the critical role of N-glycoproteins during embryonic development, differentiation, and maintenance of cell functions. CDG1M is a very severe disease with death occurring in early life. Note=The disease is caused by mutations affecting the gene represented in this entry. Similarity: Belongs to the polyprenol kinase family. Gene ID: 22845 Database links: Entrez Gene: 22845 Human Omim: 610746 Human SwissProt: Q9UPQ8 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

TMEM15/跨膜蛋白15抗体产品应用:WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复) not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.

研究领域:细胞生物  跨膜蛋白  细胞膜蛋白  

储存条件: Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

来源: Rabbit

外观: Lyophilized or Liquid


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