anti-NPC1 / Niemann Pick C1 antibody

Key features and details

  • 产品描述: Rabbit Polyclonal antibody recognizes NPC1 / Niemann Pick C1
  • 反应物种: Ms, Rat
  • 预测物种: Hu
  • 应用: WB
  • 宿主: Rabbit
  • 克隆: Polyclonal
  • 同位型: IgG
  • 靶点名称: NPC1 / Niemann Pick C1
  • 抗原物种: Human
  • Brand:
CAT.NO. : ARG59009
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Product Details
概述
产品描述Rabbit Polyclonal antibody recognizes NPC1 / Niemann Pick C1
反应物种Ms, Rat
预测物种Hu
应用WB
宿主Rabbit
克隆Polyclonal
同位型IgG
靶点名称NPC1 / Niemann Pick C1
抗原物种Human
抗原Recombinant protein corresponding to A1022-F1278 of Human NPC1 / Niemann Pick C1.
偶联标记Un-conjugated
別名Niemann-Pick C1 protein; NPC
应用说明
应用建议
应用推荐稀释比
WB0.1 - 0.5 µg/ml
应用说明* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
属性
形式Liquid
纯化Affinity purification with immunogen.
缓冲液0.2% Na2HPO4, 0.9% NaCl, 0.05% Sodium azide and 4% Trehalose.
抗菌剂0.05% Sodium azide
稳定剂4% Trehalose
浓度0.5 mg/ml
存放说明For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
注意事项For laboratory research only, not for drug, diagnostic or other use.
生物信息
数据库连接

GeneID: 18145 Mouse NPC1

Swiss-port # O35604 Mouse Niemann-Pick C1 protein

基因名称NPC1
全名Niemann-Pick disease, type C1
背景介绍This gene encodes a large protein that resides in the limiting membrane of endosomes and lysosomes and mediates intracellular cholesterol trafficking via binding of cholesterol to its N-terminal domain. It is predicted to have a cytoplasmic C-terminus, 13 transmembrane domains, and 3 large loops in the lumen of the endosome - the last loop being at the N-terminus. This protein transports low-density lipoproteins to late endosomal/lysosomal compartments where they are hydrolized and released as free cholesterol. Defects in this gene cause Niemann-Pick type C disease, a rare autosomal recessive neurodegenerative disorder characterized by over accumulation of cholesterol and glycosphingolipids in late endosomal/lysosomal compartments.[provided by RefSeq, Aug 2009]
生物功能Intracellular cholesterol transporter which acts in concert with NPC2 and plays an important role in the egress of cholesterol from the endosomal/lysosomal compartment. Both NPC1 and NPC2 function as the cellular 'tag team duo' (TTD) to catalyze the mobilization of cholesterol within the multivesicular environment of the late endosome (LE) to effect egress through the limiting bilayer of the LE. NPC2 binds unesterified cholesterol that has been released from LDLs in the lumen of the late endosomes/lysosomes and transfers it to the cholesterol-binding pocket of the N-terminal domain of NPC1. Cholesterol binds to NPC1 with the hydroxyl group buried in the binding pocket and is exported from the limiting membrane of late endosomes/ lysosomes to the ER and plasma membrane by an unknown mechanism. Binds oxysterol with higher affinity than cholesterol. May play a role in vesicular trafficking in glia, a process that may be crucial for maintaining the structural and functional integrity of nerve terminals. [UniProt]
细胞定位Late endosome membrane. [UniProt]
预测分子量142 kDa
翻译后修饰Glycosylated. [UniProt]
检测图片 (1)
  • ARG59009 anti-NPC1 / Niemann Pick C1 antibody WB image

    Western blot: 50 µg of samples under reducing conditions. Rat pancreas and NIH/3T3 lysates stained with ARG59009 anti-NPC1 / Niemann Pick C1 antibody at 0.5 µg/ml, overnight at 4°C.

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