产品资料
  首页 >>> 产品目录 >>> **学 >>> 单克隆抗体

醛缩酶A抗体

如果您对该产品感兴趣的话,可以
产品名称: 醛缩酶A抗体
产品型号: Aldolase A
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

醛缩酶A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。醛缩酶A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。


醛缩酶A抗体  的详细介绍

醛缩酶A抗体

规格:1mg/1ml

英文名: Aldolase A

别名: ALDA; Aldo1; ALDOA; ALDOA_HUMAN; Aldolase 1; Aldolase A; Aldolase A fructose bisphosphatase; Aldolase A fructose bisphosphate; FRUCTOALDOLASE A; Fructose 1 6 bisphosphate triosephosphate lyase; Fructo

分子量: 39kDa

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 Aldolase

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

细胞定位:

醛缩酶A抗体产品介绍:background: Research areas:Cancer //Cancer Metabolism //Metabolic signaling pathway < Aldolase A (fructose bisphosphate aldolase) is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3 phosphate and dihydroxyacetone phosphate. Three aldolase isozymes (A, B, and C), encoded by three different genes, are differentially expressed during development. Aldolase A is found in the developing embryo and is produced in even greater amounts in ***** muscle. Aldolase A expression is repressed in ***** liver, kidney and intestine and similar to aldolase C levels in brain and other nervous tissue. Aldolase A deficiency has been associated with myopathy and hemolytic anemia. Alternative splicing of this gene results in multiple transcript variants which encode 醛缩酶A抗体the same protein. Cellular localization:Cytoplasmic Tissue Specificity:***** liver, kidney and intestine and similar to aldolase C levels in brain and other nervous tissue. Function: Plays a key role in glycolysis and gluconeogenesis. In addition, may also function as scaffolding protein. Subunit: Homotetramer. Interacts with SNX9 and WAS. DISEASE: Glycogen storage disease 12 (GSD12) [MIM:611881]: A metabolic disorder associated醛缩酶A抗体 with increased hepatic glycogen and hemolytic anemia. It may lead to myopathy with exercise intolerance and rhabdomyolysis. Note=The disease is caused by mutations affecting the gene represented in this entry. Similarity: Belongs to the class I fructose-bisphosphate aldolase family. Gene ID: 226 Database links: Entrez Gene: 226 Human Omim: 103850 Human SwissProt: P04075 Human Unigene: 513490 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

醛缩酶A抗体产品应用:WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 Flow-Cyt=1:20-300 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:**学  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


产品留言
标题
联系人
联系电话
内容
验证码
点击换一张
注:1.可以使用快捷键Alt+S或Ctrl+Enter发送信息!
2.如有必要,请您留下您的详细联系方式!