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academy biomed/[P16] Human Apolipoprotein E (Apo E)/1232

价格
面议
货号:1232
浏览量:127
品牌:academy biomed
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商品描述
Concentration:0.9 mg / ml, determined by the Lowry method
Source:From fresh human plasma that has tested negative for Hepatitis C, HIV-I and HIV-II antibodies as well as Hepatitis surface antigens.
Purification:After series ultracentrifugations, Very Low density Lipoprotein (VLDL) is isolated from human plasma. Apo E is purified from delipidated VLDL, followed by gel-filtration. Minor impurities of other apo-proteins are then removed by antibody-Sepharose™ affinity column.
Purity:≥ 98% by SDS-PAGE
Buffer:20 mM Tris-HCl, 0.15 mM NaCl, 0.5 mM EDTA, 0.02 % NaN3, pH 7.4.
Storage:-20°C for long-term storage, 4°C for short- term storage. Aliquot to avoid repeated freezing and thawing.

 

*These products are for research or manufacturing use only, not for use in human therapeutic or diagnostic applications.

 

Importance

Apo E contains 299 amino acid residues. It is a 34-37 kDa glycosylated protein (Rall et al., 1983).

Apo E is involved with triglyceride, phospholipid, cholesteryl ester, and cholesterol transport in and out of cells and is a ligand for LDL receptors. Apo E has also been implicated in immune and nerve degeneration. It has been found to suppress lymphocyte proliferation. Late-onset familial and sporadic Alzheimer disease patients have been found to have a higher occurrence of one of the three common Apo E isoforms, Apo E4. The Apo E4 isoform has been detected in senile plaques and neurofibrillary tangles of Alzheimer disease patients. Apo E4 is associated with rapid chylomicron-remnant clearance and increased total cholesterol levels.

Rall, S C, K H Weisgraber, T L Innerarity, T P Bersot, R W Mahley, and C B Blum. "Identification of a New Structural Variant of Human Apolipoprotein E, E2(Lys146 Leads to Gln), in a Type III Hyperlipoproteinemic Subject with the E3/2 Phenotype." Journal of Clinical Investigation 72.4 (1983): 1288-297.

 

Citations

[P16]2016Yassine, Hussein N.; Feng, Qingru; Chiang, Jiarong; Petrosspour, Larissa M.; Fonteh, Alfred N.; Chui, Helena C.; Harrington, Michael G. (2016): ABCA1-Mediated Cholesterol Efflux Capacity to Cerebrospinal Fluid Is Reduced in Patients With Mild Cognitive Impairment and Alzheimer"s Disease. In Journal of the American Heart Association 5 (2). DOI: 10.1161/JAHA.115.002886.
[P16]2014O’Callaghan, Paul; Noborn, Fredrik; Sehlin, Dag; Li, Jin-ping; Lannfelt, Lars; Lindahl, Ulf; Zhang, Xiao (2014): Apolipoprotein E increases cell association of amyloid-β 40 through heparan sulfate and LRP1 dependent pathways. In Amyloid 21 (2), pp. 76–87. DOI: 10.3109/13506129.2013.879643.
[P16]2009Benyamini, Payam; Webster, Paul; Meyer, David I. (2009): Knockdown of p180 eliminates the terminal differentiation of a secretory cell line. In Molecular biology of the cell 20 (2), pp. 732–744. DOI: 10.1091/mbc.E08-07-0682.
[P16]2006Kawakami, Akio; Aikawa, Masanori; Libby, Peter; Alcaide, Pilar; Luscinskas, Francis W.; Sacks, Frank M. (2006): Apolipoprotein CIII in apolipoprotein B lipoproteins enhances the adhesion of human monocytic cells to endothelial cells. In Circulation 113 (5), pp. 691–700. DOI: 10.1161/CIRCULATIONAHA.105.591743.
academy biomed[A05]绵羊抗人类载脂蛋白AII多克隆抗体12A-S1a学院生物医学公司$ 155.00$ 155.00目录号数量1寄主物种: 羊浓度: 1毫克/毫升(OD 1.35 / 280 nm)抗原: 人类载脂蛋白AII纯化: 亲和纯化缓冲: 75 mM磷酸钠,75 mM NaCl,0.5 mM EDTA,0.02%NaN3,pH 7.2特异性 与人载脂蛋白AII特异性结合。免疫印迹和ELISA的稀释范围:1,000至80,000。用: 该抗体可用于检测血浆和脂蛋白中的载脂蛋白AII,免疫测定,免疫印迹,酶结合或生物素化。存储: -20°C长期保存,4°C短期保存。等分试样,以避免反复冻结和解冻。 *这些产品仅用于研究或制造用途,不能用于人体治疗或诊断应用。 重要性Apo AII占HDL的25%。它在人血浆中以77条氨基酸残基的2条相同链的二聚体形式存在,并通过二硫键连接。据报道,单链的分子量为8.7kDa(Brewer等,1972)。对小鼠的研究报道,apoAII可能具有促动脉粥样硬化作用(Warden等,1993)。然而,一项大型的欧洲前瞻性研究中的病例对照研究表明,血浆Apo AII浓度与冠心病事件密切相关(Birjmohun等,2007)。Birjmohun,RS,GM Dallinga-Thie,JA Kuivenhoven,ESg Stroes,JD Otvos,NJ Wareham,R.Luben,JJp Kastelein,K.-T. Khaw和SM Boekholdt。“载脂蛋白A-II与未来冠状动脉疾病的风险成反比。” 循环116(2007):2029-035。Brewer,HB,SE Lux,R.Ronan和KM John。“人ApoLp-Gln-II(apoA-II),一种从高密度脂蛋白复合物中分离的载脂蛋白的氨基酸序列。” 美国国家科学院院刊69.5(1972):1304-308。Warden,C.,C.Hedrick,J.Qiao,L.Castellani和A.Lusis。“过表达载脂蛋白A-II的转基因小鼠中的动脉粥样硬化。” 科学261(1993):469-72。