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品种反应性 主要应用 宿主 格式 抗体类型 H WB Gt Serum Polyclonal Antibody 描述 产品目录编号 AB740 品牌系列 Chemicon®
商名 - Chemicon
描述 Anti-Apolipoprotein A-I Antibody Alternate Names - ApoAI
产品信息 格式 Serum 演示 Goat serum defibrinated, delipidized and adsorbed by solid phase chromatography as required. Liquid in 0.05M Tris-HCl, pH 7.5, 0.5M NaCl with 0.1% sodium azide. 应用 应用 This Anti-Apolipoprotein A-I Antibody is validated for use in WB for the detection of Apolipoprotein A-I. 主要应用 - Western Blotting
应用说明 Optimal working dilutions must be determined by the end user. 生物信息 免疫原品种 Purified human apolipoprotein A-I 宿主 Goat 特异性 Human apolipoprotein A-I. Monospecific by IEP. 品种反应性 Human 抗体类型 Polyclonal Antibody Entrez基因编号 - NM_000039.1
Entrez基因汇总 This gene encodes apolipoprotein A-I, which is the major protein component of high density lipoprotein (HDL) in plasma. The protein promotes cholesterol efflux from tissues to the liver for excretion, and it is a cofactor for lecithin cholesterolacyltransferase (LCAT) which is responsible for the formation of most plasma cholesteryl esters. This gene is closely linked with two other apolipoprotein genes on chromosome 11. Defects in this gene are associated with HDL deficiencies, including Tangier disease, and with systemic non-neuropathic amyloidosis. 基因符号 - Apo-AI
- APOA1
- ApoA-I
- MGC117399
- preproapolipoprotein
- amyloidosis
UniProt编号 - P02647
UniProt汇总 FUNCTION: SwissProt: P02647 # Participates in the reverse transport of cholesterol from tissues to the liver for excretion by promoting cholesterol efflux from tissues and by acting as a cofactor for the lecithin cholesterol acyltransferase (LCAT).
SIZE: 267 amino acids; 30778 Da
SUBUNIT: Interacts with APOA1BP.
SUBCELLULAR LOCATION: Secreted.
TISSUE SPECIFICITY: Major protein of plasma HDL, also found in chylomicrons. Synthesized in the liver and small intestine.
PTM: Palmitoylated.
DISEASE: SwissProt: P02647 # Defects in APOA1 are a cause of high density lipoprotein deficiency type 2 (HDLD2) [MIM:604091]; also known as familial hypoalphalipoproteinemia (FHA). Inheritance is autosomal dominant. & Defects in APOA1 are a cause of the low HDL levels observed in high density lipoprotein deficiency type 1 (HDLD1) [MIM:205400]; also known as analphalipoproteinemia or Tangier disease (TGD). HDLD1 is a recessive disorder characterized by the absence of plasma HDL, accumulation of cholesteryl esters, premature coronary artery disease, hepatosplenomegaly, recurrent peripheral neuropathy and progressive muscle wasting and weakness. In HDLD1 patients, ApoA-I fails to associate with HDL probably because of the faulty conversion of pro-ApoA-I molecules into mature chains, either due to a defect in the converting enzyme activity or a specific structural defect in Tangier ApoA-I. & Defects in APOA1 are a cause of systemic non-neuropathic amyloidosis [MIM:105200]; also known as amyloidosis VIII or Ostertag-type amyloidosis. It is an autosomal dominant disorder characterized by generalized amyloid deposition.
SIMILARITY: SwissProt: P02647 ## Belongs to the apolipoprotein A1/A4/E family.产品使用声明 使用声明 - Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
储存和货运信息 存储条件 Maintain at -20°C in undiluted aliquots for up to 12 months. Avoid repeated freeze/thaw cycles. 包装信息 数量 1 mL
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