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BSPRY蛋白抗体

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产品名称: BSPRY蛋白抗体
产品型号: BSPRY
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

BSPRY蛋白抗体应用于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。BSPRY蛋白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。


BSPRY蛋白抗体  的详细介绍

BSPRY蛋白抗体

规格:1mg/1ml

英文名: BSPRY

别名: B box and SPRY domain containing; B box and SPRY domain containing protein; B box and SPRY domain-containing protein; B-box and SPRY domain containing; Bspry; BSPRY_HUMAN; FLJ20150; Zetin 1.

分子量: 44kDa

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 BSPRY

交叉反应:Human, Mouse, Rat,

细胞定位:细胞浆 细胞膜

BSPRY蛋白抗体产品介绍:background: BSPRY is a 402 amino acid protein that localizes to both the membrane and the cytoplasm and contains one B box-type zinc finger and one B30.2/SPRY domain. Existing as two alternatively spliced isoforms, BSPRY interacts with TRPV5 and TRPV6 and is thought to regulate the transport of calcium across the epithelium, probably by inhibiting the activity of TRPV proteins. The gene encoding BSPRY maps to human chromosome 9, which houses over 900 genes and comprises nearly 4% of the human genome. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Function: BSPRY is a 402 amino acid protein that localizes to both the membrane and the cytoplasm and contains one B box-type zinc finger and one B30.2/SPRY domain. Existing as two alternatively spliced isoformsBSPRY蛋白抗体 BSPRY interacts with TRPV5 and TRPV6 and is thought to regulate the transport of calcium across the epithelium, probably by inhibiting the activity of TRPV proteins. The gene encoding BSPRY maps to human chromosome 9, which houses over 900 genes and comprises nearly 4% of the human genome. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Subcellular BSPRY蛋白抗体Location: Cytoplasm. Membrane. Similarity: Contains 1 B box-type zinc finger. Contains 1 B30.2/SPRY domain. Gene ID: 54836 Database links: Entrez Gene: 54836 Human SwissProt: Q5W0U4 Human Unigene: 614517 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

BSPRY蛋白抗体产品应用: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:肿瘤  细胞生物  信号转导  

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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