全国空降,快活林手机版登录入口,加qq群快餐妹同城约跑16以上,全国ww招聘大圈

产品资料
  首页 >>> 产品目录 >>> **学 >>> 单克隆抗体

载脂蛋白A5抗体

如果您对该产品感兴趣的话,可以
产品名称: 载脂蛋白A5抗体
产品型号: Apolipoprotein A V
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

载脂蛋白A5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。载脂蛋白A5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。


载脂蛋白A5抗体  的详细介绍

载脂蛋白A5抗体

规格:1mg/1ml

英文名: Apolipoprotein A V

别名: APOA5; Apolipoprotein A V; Apo-AV; ApoA-V; Apoa5; APOA5_HUMAN; ApoAV; Apolipoprotein A-V; Apolipoprotein A5; RAP3; Regeneration associated protein 3; Regeneration-associated protein 3.

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 APOA5

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

细胞定位:分泌型蛋白

载脂蛋白A5抗体产品介绍:background: The protein encoded by this gene is an apolipoprotein that plays an important role in regulating the plasma triglyceride levels, a major risk factor for coronary artery disease. It is a component of high density lipoprotein and is highly similar to a rat protein that is upregulated in response to liver injury. Mutations in this gene have been associated with hypertriglyceridemia and hyperlipoproteinemia type 5. This gene is located proximal to the apolipoprotein gene cluster on chromosome 11q23. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Oct 2009]. Function: Minor apolipoprotein mainly associated with HDL and to a lesser extent with VLDL. May also be associated with chylomicrons. Important determinant of plasma triglyceride (TG) levels by both being a potent stimulator of apo-CII lipoprotein lipase (LPL) TG hydrolysis and a inhibitor of the hepatic VLDL-TG production rate (without affecting the VLDL-apoB production rate). Activates poorly lecithin:cholesterol acyltransferase (LCAT) and does not enhance efflux of cholesterol from macrophages.载脂蛋白A5抗体 Subunit: Interacts with GPIHBP1. Subcellular Location: Secreted. Tissue Specificity: Liver and plasma. Post-translational modifications: Phosphorylation sites are present in the extracellular medium. DISEASE: Defects in APOA5 are a cause of hyperlipoproteinemia type 5 (HLPP5) [MIM:144650]. HLPP5 is characterized by increased amounts of chylomicrons and very low density lipoprotein (VLDL) and decreased low density lipoprotein (LDL) and high density lipoprotein (HDL) in the plasma after a fast. Numerous conditions cause this phenotype, including insulin-dependent 载脂蛋白A5抗体diabetes mellitus, contraceptive steroids, alcohol abuse, and glycogen storage disease type 1A (GSD1A) [MIM:232200]. Similarity: Belongs to the apolipoprotein A1/A4/E family. Database links: Entrez Gene: 116519 Human Omim: 606368 Human SwissProt: Q6Q788 Human Unigene: 283923 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

载脂蛋白A5抗体产品应用:WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=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  **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!