首页 >>> 产品目录 >>> **学 >>> 单克隆抗体
仪表展览网 >>> 展馆展区 >>> 试剂 >>> **试剂 >>> 钠钾离子转运蛋白1抗体
> 钠钾离子转运蛋白1抗体

产品资料

钠钾离子转运蛋白1抗体

钠钾离子转运蛋白1抗体
  • 如果您对该产品感兴趣的话,可以
  • 产品名称:钠钾离子转运蛋白1抗体
  • 产品型号: NKCC1/SLC12A2
  • 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
钠钾离子转运蛋白1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。钠钾离子转运蛋白1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。
产品描述

钠钾离子转运蛋白1抗体

规格:1mg/1ml

英文名: NKCC1/SLC12A2

别名: Basolateral Na-K-Cl symporter; BSC; BSC2; Bumetanide-sensitive sodium-(potassium)-chloride cotransporter 1; mBSC2; NKCC1; S12A2_HUMAN; SLC12A2; sodium-potassium-chloride cotransporter 1; solute carrie

分子量: 133kDa

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 NKCC1

交叉反应:Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Chimpanzee,

细胞定位:细胞膜

钠钾离子转运蛋白1抗体产品介绍:background: Na-K-Cl cotransporters (NKCC) are channel proteins that aid in the transcellular movement of chloride across both secretory and absorptive epithelia. NKCC1 is expressed in muscle cells, neurons, and red blood cells. In the basolateral membrane of secretory epithelia, NKCC1 mediates active chloride secretion. The gene encoding human NKCC1 maps to chromosome 5q23.3. In mice, disruption of the NKCC1 gene leads to deafness and impaired balance. NKCC2 is specifically expressed in the kidney where it mediates active reabsorption of sodium chloride in the thick ascending limb of the loop of Henle. NKCC2 is sensitive to the clinically important diuretics furosemide and bumetanide. The gene encoding human NKCC2 maps to chromosome 15q15-q21 and mutations in this gene lead to Bartter’s syndrome, an inherited hypokalaemic alkalosis. NCCT is a thiazide-sensitive Na-Cl cotransporter that is primarily expressed in the distal convoluted tubule of the kidney where it accounts for a significant fraction of net renal sodium reabsorption. The gene for human NCCT map to chromosome钠钾离子转运蛋白1抗体 16q13. Mutations in the gene encoding NCCT cause Gitelman’s syndrome, a subset of Bartter’s syndrome. Function: Electrically silent transporter system. Mediates sodium and chloride reabsorption. Plays a vital role in the regulation of ionic balance and cell volume. Subcellular Location: Membrane; Multi-pass membrane protein. Tissue Specificity: Expressed in many tissues. Post-translational modifications: Phosphorylated upon DNA damage, probably by ATM or ATR. Similarity: Belongs to the SLC12A transporter family. Database links: Entrez Gene: 471620 Chimpanzee Entrez Gene: 286845 Cow Entrez Gene: 481490 Dog Entrez Gene: 6558 Human Entrez Gene: 20496 Mouse Entrez Gene: 100516960 Pig Entrez Gene: 钠钾离子转运蛋白1抗体83629 Rat Omim: 600840 Human SwissProt: P55011 Human SwissProt: P55012 Mouse Unigene: 162585 Human Unigene: 712970 Human Unigene: 399997 Mouse Unigene: 11523 Rat Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

钠钾离子转运蛋白1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  心血管  细胞生物  神经生物学  信号转导  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!
  • 温馨提示:为规避购买风险,建议您在购买前务必确认供应商资质与产品质量。
  • 免责申明:以上内容为注册会员自行发布,若信息的真实性、合法性存在争议,平台将会监督协助处理,欢迎举报
产品留言
标题
内容
联系人
联系电话
电子邮件
公司名称
联系地址
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!