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academy biomed/[A07] Goat Anti-Human Apolipoprotein B-100 Polyclonal Antibody/1.0 mg/20A-G1b

价格
¥17480.00
货号:20A-G1b
浏览量:127
品牌:academy biomed
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商品描述
Host Species:Goat
Concentration:1 mg/ml (OD 1.35 / 280 nm)
Antigen:Human Apolipoprotein B100
Purification:Affinity purified
Buffer:75 mM Sodium Phosphate, 75 mM NaCl, 0.5 mM EDTA, 0.02% NaN3, pH 7.2
SpecificitySpecifically binds to human apo B-100. Dilution for immunoblot and ELISA range: 1,000 to 80,000.
Use:The antibody can be used for detection of apo B-100 in plasma and lipoproteins, immunoassays, immunoblots, enzyme conjugation, or biotinylation.
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

ApoB exists in human plasma in two isoforms, ApoB-48 (Chen et al., 1987) and Apo B-100 (Wei et al., 1985, Yang et al., 1986a; 1989a,b; 1990; Chen et al., 1986; Yang et al., 1990, Yang and Pownall, 1992). Apo B-100 is the major physiological ligand for the LDL receptor. Apo B-100 is a large monomeric protein, containing 4536 amino acids (m.w. 515 kDa, Yang et al., 1986b).

Apo B-100 is synthesized in the liver and is required for the assembly of VLDL. It is found in LDL and VLDL after the removal of the Apo A, E and C. Apo B-48 is present in chylomicrons and their remnants. It is essential for the intestinal absorption of dietary lipids. Apo B levels correlate with the risk of coronary disease.

The Apo B protein is directly involved in the retention of LDL with the arterial wall (Olofsson and Boren, 2012). Apo B-48 is synthesized in the small intestine. It comprises approximately half of the N-terminal region of ApoB-100 and is the result of posttranscriptional mRNA editing by a stop codon in the intestine not found in the liver.

Chen, S., G. Habib, C. Yang, Z. Gu, B. Lee, S. Weng, S. Cai, J. Deslypere, M. Rosseneu, and Al. Et. "Apolipoprotein B-48 Is the Product of a Messenger RNA with an Organ-specific In-frame Stop Codon." Science 238 (1987): 363- 66.

Olofsson, S.-O., and J. Boren. "Apolipoprotein B Secretory Regulation by Degradation." Arteriosclerosis, Thrombosis, and Vascular Biology 32 (2012): 1334-338.

Wei, C. F., S. H. Chen, C. Y. Yang, Y. L. Marcel, R. W. Milne, W. H. Li, J. T. Sparrow, A. M. Gotto, and L. Chan. "Molecular Cloning and Expression of Partial cDNAs and Deduced Amino Acid Sequence of a Carboxyl-terminal Fragment of Human Apolipoprotein B-100." Proceedings of the National Academy of Sciences 82 (1985): 7265- 269.

Yang, Chao-Yuh, and Pownall, H.J. "In Structure and Function of Plasma Apolipoproteins." Structure and Function of Apolipoproteins. Boca Raton, Fla.: CRC, 1992.

Yang, Chao-Yuh, T. W. Kim, S. A. Weng, B. R. Lee, M. L. Yang, and A. M. Gotto. "Isolation and Characterization of Sulfhydryl and Disulfide Peptides of Human Apolipoprotein B-100." Proceedings of the National Academy of Sciences 87 (1990): 5523-527.

Yang, Chao-Yuh, Z. W. Gu, S. A. Weng, T. W. Kim, S. H. Chen, H. J. Pownall, P. M. Sharp, S. W. Liu, W. H. Li, and A. M. Gotto. "Structure of Apolipoprotein B-100 of Human Low Density Lipoproteins." Arteriosclerosis, Thrombosis, and Vascular Biology 9 (1989a): 96-108.

Yang, Chao-Yuh, Zi-Wei Gu, Lawrence Chan, Henry J. Pownall, and Antonio M. Gotto. "Structure and Functional Domains of Human Apolipoprotein B-100: A Strategy to Elucidate the Structure Information of a Large Protein." Methods in Protein Sequence Analysis (1989b): 466-74.

Yang, Chao-Yuh, San-Hwan Chen, Sandra H. Gianturco, William A. Bradley, James T. Sparrow, Masako Tanimura, Wen-Hsiung Li, Doris A. Sparrow, Hans Deloof, Maryvonne Rosseneu, Fu-Shin Lee, Zi-Wei Gu, Antonio M. Gotto, and Lawrence Chan. "Sequence, Structure, Receptor-binding Domains and Internal Repeats of Human Apolipoprotein B-100." Nature 323 (1986a): 738-42.

 

Citations

[A07]2020

Walsh, Meghan T.; Celestin, Oni M.; Thierer, James H.; Rajan, Sujith; Farber, Steven A.; Hussain, M. Mahmood (2020): Model systems for studying the assembly, trafficking, and secretion of apoB lipoproteins using fluorescent fusion proteins. In J. Lipid Res. 61 (3), pp. 316–327. DOI: 10.1194/jlr.RA119000259.

[A07]2020

Liu, Gang; Zhang, Bo; Hu, Yang; Rood, Jennifer; Liang, Liming; Qi, Lu et al. (2020): Associations of Perfluoroalkyl substances with blood lipids and Apolipoproteins in lipoprotein subspecies: the POUNDS-lost study. In Environmental Health : A Global Access Science Source 19 (1), p. 5. DOI: 10.1186/s12940-020-0561-8.

[A07]2020

Chen, Wei-Yu; Chen, Yun-Fang; Chan, Hua-Cheng; Chung, Ching-Hu; Peng, Hsien-Yu; Ho, Yu-Cheng et al. (2020): Role of apolipoprotein E in electronegative low-density lipoprotein-induced mitochondrial dysfunction in cardiomyocytes. In Metabolism: Clinical and Experimental 107, p. 154227. DOI: 10.1016/j.metabol.2020.154227.

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[A07]2014Lee, An-Sheng; Chen, Wei-Yu; Chan, Hua-Chen; Hsu, Jing-Fang; Shen, Ming-Yi; Chang, Chia-Ming et al. (2014): Gender disparity in LDL-induced cardiovascular damage and the protective role of estrogens against electronegative LDL. In Cardiovascular Diabetology 13, p. 64. DOI: 10.1186/1475-2840-13-64.
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[A07]2014Yang, Tzu-Ching; Chen, Yi-Jie; Chang, Shwu-Fen; Chen, Chu-Huang; Chang, Po-Yuan; Lu, Shao-Chun (2014): Malondialdehyde mediates oxidized LDL-induced coronary toxicity through the Akt-FGF2 pathway via DNA methylation. In Journal of Biomedical Science 21, p. 11. DOI: 10.1186/1423-0127-21-11.
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[A07]2013Sumner, Anne E.; Furtado, Jeremy D.; Courville, Amber B.; Ricks, Madia; Younger-Coleman, Novie; Tulloch-Reid, Marshall K.; Sacks, Frank M. (2013): ApoC-III and visceral adipose tissue contribute to paradoxically normal triglyceride levels in insulin-resistant African-American women. In Nutrition & Metabolism 10 (1), p. 73. DOI: 10.1186/1743-7075-10-73.
[A07]2012Avraham-Davidi, Inbal; Ely, Yona; van Pham, N.; Castranova, Daniel; Grunspan, Moshe; Malkinson, Guy et al. (2012): ApoB-containing lipoproteins regulate angiogenesis by modulating expression of VEGF receptor 1. In Nature Medicine 18 (6), pp. 967–973. DOI: 10.1038/nm.2759.
[A07]2012Shen, Xun; Wang, Wei; Wang, Liangsu; Houde, Caroline; Wu, Weizhen; Tudor, Matt et al. (2012): Identification of genes affecting apolipoprotein B secretion following siRNA-mediated gene knockdown in primary human hepatocytes. In Atherosclerosis 222 (1), pp. 154–157. DOI: 10.1016/j.atherosclerosis.2012.02.012.
[A07]2012Wang, Min S.; Messersmith, Reid E.; Reed, Scott M. (2012): Membrane curvature recognition by C-reactive protein using lipoprotein mimics. In Soft Matter 8 (30), pp. 7909–7918. DOI: 10.1039/C2SM25779C.
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[A07]2008Seki, Takenori; Kunichika, Tomoya; Watanabe, Kiyotaka; Orino, Koichi (2008): Apolipoprotein B binds ferritin by hemin-mediated binding: evidence of direct binding of apolipoprotein B and ferritin to hemin. In Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine 21 (1), pp. 61–69. DOI: 10.1007/s10534-007-9093-8.
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[A07]2007Temel, Ryan E.; Tang, Weiqing; Ma, Yinyan; Rudel, Lawrence L.; Willingham, Mark C.; Ioannou, Yiannis A. et al. (2007): Hepatic Niemann-Pick C1-like 1 regulates biliary cholesterol concentration and is a target of ezetimibe. In The Journal of clinical investigation 117 (7), pp. 1968–1978. DOI: 10.1172/JCI30060.
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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。