anti-LPL / Lipoprotein Lipase antibody [5D2] (low endotoxin)

Key features and details

  • 产品描述: Azide free and low endotoxin Mouse Monoclonal antibody [5D2] recognizes LPL / Lipoprotein Lipase
  • 反应物种: Hu, Rat, Bov, Chk, Gpig
  • 不反应物种: Ms
  • 应用: ELISA, FuncSt, IP, WB
  • 宿主: Mouse
  • 克隆: Monoclonal
  • 克隆号: 5D2
  • 同位型: IgG1
  • 靶点名称: LPL / Lipoprotein Lipase
  • Brand:
CAT.NO. : ARG23654
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Product Details
概述
产品描述Azide free and low endotoxin Mouse Monoclonal antibody [5D2] recognizes LPL / Lipoprotein Lipase
反应物种Hu, Rat, Bov, Chk, Gpig
不反应物种Ms
应用ELISA, FuncSt, IP, WB
宿主Mouse
克隆Monoclonal
克隆号5D2
同位型IgG1
靶点名称LPL / Lipoprotein Lipase
抗原物种Bovine
抗原Purified Bovine milk lipoprotein lipase.
偶联标记Un-conjugated
別名EC 3.1.1.34; LPL; Lipoprotein lipase; LIPD; HDLCQ11
应用说明
应用建议
应用推荐稀释比
ELISA1:500 - 1:5000
FuncStAssay-dependent
IPAssay-dependent
WBAssay-dependent
应用说明WB: This product detects a band of ~ 53 kDa using partially purified LPL from postheparin plasma.
ELISA: This product can be used in an indirect ELISA, or as the capture antibody in a sandwich ELISA.
* 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Purification with Protein G.
纯化说明Low endotoxin
缓冲液PBS.
浓度1 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: 100135570 Guinea pig LPL

GeneID: 24539 Rat LPL

GeneID: 280843 Bovine LPL

基因名称LPL
全名lipoprotein lipase
背景介绍LPL encodes lipoprotein lipase, which is expressed in heart, muscle, and adipose tissue. LPL functions as a homodimer, and has the dual functions of triglyceride hydrolase and ligand/bridging factor for receptor-mediated lipoprotein uptake. Severe mutations that cause LPL deficiency result in type I hyperlipoproteinemia, while less extreme mutations in LPL are linked to many disorders of lipoprotein metabolism. [provided by RefSeq, Jul 2008]
生物功能The primary function of this lipase is the hydrolysis of triglycerides of circulating chylomicrons and very low density lipoproteins (VLDL). Binding to heparin sulfate proteogylcans at the cell surface is vital to the function. The apolipoprotein, APOC2, acts as a coactivator of LPL activity in the presence of lipids on the luminal surface of vascular endothelium (By similarity). [UniProt]
预测分子量53 kDa
翻译后修饰Tyrosine nitration after lipopolysaccharide (LPS) challenge down-regulates the lipase activity. [UniProt]
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