anti-Galactosidase alpha antibody

Key features and details

  • 产品描述: Rabbit Polyclonal antibody recognizes Galactosidase alpha
  • 反应物种: Hu, Ms
  • 应用: ICC/IF, WB
  • 宿主: Rabbit
  • 克隆: Polyclonal
  • 同位型: IgG
  • 靶点名称: Galactosidase alpha
  • 抗原物种: Human
  • 抗原: Recombinant fusion protein corresponding to aa. 150-429 of Human Galactosidase alpha (NP_000160.1).
  • Brand:
CAT.NO. : ARG58844
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Product Details
概述
产品描述Rabbit Polyclonal antibody recognizes Galactosidase alpha
反应物种Hu, Ms
应用ICC/IF, WB
宿主Rabbit
克隆Polyclonal
同位型IgG
靶点名称Galactosidase alpha
抗原物种Human
抗原Recombinant fusion protein corresponding to aa. 150-429 of Human Galactosidase alpha (NP_000160.1).
偶联标记Un-conjugated
別名Alpha-galactosidase A; Melibiase; Alpha-D-galactosidase A; Alpha-D-galactoside galactohydrolase; EC 3.2.1.22; Agalsidase; GALA
应用说明
应用建议
应用推荐稀释比
ICC/IF1:50 - 1:100
WB1:500 - 1:1000
应用说明* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
实际分子量49 kDa
属性
形式Liquid
纯化Affinity purified.
缓冲液PBS (pH 7.3), 0.02% Sodium azide and 50% Glycerol.
抗菌剂0.02% Sodium azide
稳定剂50% Glycerol
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. 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: 2717 Human GLA

Swiss-port # P06280 Human Alpha-galactosidase A

基因名称GLA
全名galactosidase, alpha
背景介绍This gene encodes a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. This enzyme predominantly hydrolyzes ceramide trihexoside, and it can catalyze the hydrolysis of melibiose into galactose and glucose. A variety of mutations in this gene affect the synthesis, processing, and stability of this enzyme, which causes Fabry disease, a rare lysosomal storage disorder that results from a failure to catabolize alpha-D-galactosyl glycolipid moieties. [provided by RefSeq, Jul 2008]
细胞定位Lysosome. [UniProt]
预测分子量49 kDa
检测图片 (1)
  • ARG58844 anti-Galactosidase alpha antibody ICC/IF image

    Immunofluorescence: HeLa cells stained with ARG58844 anti-Galactosidase alpha antibody.

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