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- 详细信息
- 询价记录
- 文献和实验
- 技术资料
- 克隆性:
多克隆
- 抗体英文名:
ApoE4 Antibody,Apolipoprotein E4,APOE 4,APOE4,APOE-4
- 规格:
100 ug
产品名称:ApoE4抗体|ApoE4 Antibody,Apolipoprotein E4,APOE 4,APOE4,APOE-4
【产品形式】:艾美捷为您提供的ApoE4抗体产品为100 ug 无色溶液,其浓度为0.5 mg/ml,溶解于包含有30%甘油, 0.5% BSA, 0.01%硫柳汞 的PBS (pH 7.2)缓冲液中.请将该ApoE4抗体产品置于-20 ℃冷冻保存,建议分装使用以避免反复冻融.
【背景资料】:ApoE belongs to a group of proteins that bind reversibly with lipoprotein and play an important role in lipid metabolism. In addition to facilitating solublization of lipids, these proteins help to maintain the structural integrity of lipoproteins, serve as ligands for lipoprotein receptors, and regulate the activity of enzymes involved in lipid metabolism. Significant quantities of ApoE are produced in liver and brain and to some extent in almost every organ. ApoE is an important constituent of all plasma lipoproteins. It’s interaction with specific ApoE receptor enables uptake of chylomicron remnants by liver cells, which is an essential step during normal lipid metabolism. It also binds with the LDL receptor (apo B/E). Defects in ApoE are a cause of hyperlipoproteinemia type III. ApoE exists in three major isoforms; E2, E3, and E4, which differ from one another by a single amino-acid substitution. Individuals heterozygous for the ApoE4 allele are at higher risk of late-onset Alzheimer’s disease.
BioVision的公司总部在美丽的旧金山湾地区,它是全球生命科学公司的领导者.BioVision在开发和研究细胞凋亡检测分析、代谢检测方面具有 卓越的影响力.包括检测各种检测分析试剂盒、相关特色抗体、重组蛋白及细胞因子和酶等多种产品,以及其他创新的研究工具.其产品覆盖细胞凋亡研究、能量代 谢、细胞/组织蛋白提取、氧化应激与损伤、代谢与肥胖症、细胞增殖与毒性、信号转导、干细胞研究等领域.作为多家知名品牌的中国总代理以及中国区域代理, 艾美捷与BioVision一起为研究者们提供最好、最新的细胞生物学研究工具而不断扩大产品及服务质量.
点击:ApoE4抗体,查看更详细产品说明,更多应用、储存、价格、货期等信息请致电400-6800-868垂询BioVision中国区域授权总代理艾美捷科技有限公司。
关键词:ApoE,ApoE4抗体
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文献和实验施一公团队 2023 首秀!发现 APOE4 受体,揭示阿尔兹海默症潜在致病因子
导读 APOE 的基因产物 APOE 在脂质代谢、免疫调节和神经学中起着关键作用。最常见的三种 APOE 等位基因对应于三种蛋白质异构体,分别是 APOE2、APOE3 和 APOE4,它们仅在 112 和 158 两个氨基酸位置上存在差异。尽管只存在微小差别,但前期的研究数据表明,这些 APOE 亚型在生理和病理学层面却表现出不同的作用。 其中,APOE 的免疫调节作用最初是作为血浆脂蛋白对 T 细胞增殖抑制作用的一部分被发现的。研究表明,APOE 能够抑制 T 细胞增殖和中
APOE-Based Models of Pre-Dementia
Producing a valid animal model of apolipoprotein E (APOE )-based dementia is critical to understanding the etiology and progression of late-onset Alzheimer’s disease (AD). Unfortunately, no such model exists. Herein, I review
Laser-Capture Microdissection of Hyperlipidemic/ApoE/ Mouse Aorta Atherosclerosis
roles have not been defined. To map these infiltrates, we employed laser-capture microdissection (LCM) to isolate the three arterial wall laminae using apoE−/− mouse aorta as a model. RNA from LCM-separated tissues was extracted and large-scale
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