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绒毛膜特异性转录因子GCM2抗体

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产品名称: 绒毛膜特异性转录因子GCM2抗体
产品型号: GCM2
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

绒毛膜特异性转录因子GCM2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。绒毛膜特异性转录因子GCM2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。


绒毛膜特异性转录因子GCM2抗体  的详细介绍

绒毛膜特异性转录因子GCM2抗体

规格:1mg/1ml

英文名: GCM2

别名: Chorion-specific transcription factor GCMb; GCM motif protein 2; GCMb; Glial cells missing homolog 2; glial cells missing homolog b; GCM2_HUMAN.

分子量: 57kDa

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 GCM2

交叉反应:Human, Mouse, Rat, Dog, Horse, Rabbit,

细胞定位:细胞核

绒毛膜特异性转录因子GCM2抗体产品介绍:background: Glial cells missing homolog 2 (GCM2), also known as Chorion-specific transcription factor GCMb, is a 506 amino acid nuclear protein. GCM2 is a transcription factor that acts as an essential regulator of parathyroid development. GCM2 is also thought to mediate the effect of calcium on parathyroid hormone expression and secretion in parathyroid cells. GCM2 contains one N-terminal GCM domain, which has DNA binding activity. Mutations of the gene that encodes GCM2 are associated with hypoparathyroidism, an autosomal recessive condition characterized by hypocalcemia and hyperphosphatemia. Function: Gcm2, a mouse ortholog of the绒毛膜特异性转录因子GCM2抗体 Drosophila Glial Cells Missing gene, is expressed in the parathyroid-specific domains in the 3rd pouches from E9.5. The null mutation of Gcm2 causes aparathyroidism in the fetal and ***** mouse and has been proposed to be a master regulator for parathyroid development. During Drosophila embryogenesis Gcm2 plays a crucial role in promoting glial cell differentiation. Subcellular Location: Nuclear绒毛膜特异性转录因子GCM2抗体. DISEASE: Defects in GCM2 are a cause of familial isolated hypoparathyroidism (FIH) [MIM:146200]; also known as autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. An autosomal recessive form of FIH also exists. Similarity: Contains 1 GCM DNA-binding domain. Database links: UniProtKB/Swiss-Prot: O75603.1 Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

绒毛膜特异性转录因子GCM2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  发育生物学  干细胞  转录调节因子  

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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