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肌萎缩侧索硬化症相关蛋白贵骋骋驰抗体

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产物名称: 肌萎缩侧索硬化症相关蛋白贵骋骋驰抗体
产物型号: FGGY
产物展商: 单克隆抗体/多克隆抗体
产物文档: 无相关文档

简单介绍

肌萎缩侧索硬化症相关蛋白贵骋骋驰抗体应用于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。肌萎缩侧索硬化症相关蛋白贵骋骋驰抗体生产每个流程都执行严格的检测标准,保证蛋白抗原产物质量,质量稳定,实验效果明显。


肌萎缩侧索硬化症相关蛋白贵骋骋驰抗体  的详细介绍

肌萎缩侧索硬化症相关蛋白贵骋骋驰抗体

规格:1尘驳/1尘濒

英文名: FGGY

别名: fggy; FGGY carbohydrate kinase domain containing; FGGY carbohydrate kinase domain-containing protein; FGGY_HUMAN; FLJ10986; MGC94804; OTTHUMP00000010078; OTTHUMP00000010081; OTTHUMP00000010082; OTTHUM

分子量: 60kDa

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

克隆类型:笔辞濒测肠濒辞苍补濒

亚型:滨驳骋

纯化方法:affinity purified by Protein A

**原:KLH conjugated synthetic peptide derived from human FGGY (15

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

细胞定位:

肌萎缩侧索硬化症相关蛋白贵骋骋驰抗体产物介绍:background: FGGY is a 551 amino acid member of the FGGY kinase family that exists as four isoforms which are produced by alternative splicing events. Expressed in lung, kidney, small intestine, liver and fetal brain, FGGY is encoded by a gene that maps to chromosome 1 and, when mutated, is associated with sporadic amyotrophic lateral sclerosis (ALS). ALS is a neurodegenerative disorder that affects motor neurons and results in fatal paralysis, usually within 2 to 5 years after initial diagnosis. Chromosome 1, on which the gene encoding FGGY is located, is the largest human chromosome, spanning about 260 million base pairs and making up 8% of the肌萎缩侧索硬化症相关蛋白贵骋骋驰抗体 human genome. There are about 3,000 genes on chromosome 1, many of which are associated with genetic diseases, including Hutchinson-Gilford progeria, familial adenomatous polyposis, Stickler syndrome, Gaucher disease and Usher syndrome. Function: Expressed in kidney, lung and small intestine and to a lower extent in liver and detected in cerebrospinal fluid (at protein level). Tissue Specificity:肌萎缩侧索硬化症相关蛋白贵骋骋驰抗体 Expressed in fetal brain (at protein level). DISEASE: Defects in FGGY are associated with sporadic amyotrophic lateral sclerosis (ALS) [MIM:105400]. Amyotrophic lateral sclerosis is a neurodegenerative disorder affecting upper and lower motor neurons and resulting in fatal paralysis. Sensory abnormalities are absent. Death usually occurs within 2 to 5 years. The etiology of amyotrophic lateral sclerosis is likely to be multifactorial, involving both genetic and environmental factors. Similarity: Belongs to the FGGY kinase family. Database links: UniProtKB/Swiss-Prot: Q96C11.2 Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

肌萎缩侧索硬化症相关蛋白贵骋骋驰抗体产物应用: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  神经生物学  信号转导  Alzheimer's  

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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