anti-HEXA antibody [20F1]

Key features and details

  • 产品描述: Mouse Monoclonal antibody [20F1] recognizes HEXA
  • 反应物种: Hu
  • 应用: FACS, WB
  • 宿主: Mouse
  • 克隆: Monoclonal
  • 克隆号: 20F1
  • 同位型: IgG2a, lambda
  • 靶点名称: HEXA
  • 抗原物种: Human
  • Brand:
CAT.NO. : ARG57022
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Product Details
概述
产品描述Mouse Monoclonal antibody [20F1] recognizes HEXA
反应物种Hu
应用FACS, WB
宿主Mouse
克隆Monoclonal
克隆号20F1
同位型IgG2a, lambda
靶点名称HEXA
抗原物种Human
抗原Recombinant fragment around aa. 89-529 of Human HEXA.
偶联标记Un-conjugated
別名N-acetyl-beta-glucosaminidase subunit alpha; Beta-N-acetylhexosaminidase subunit alpha; EC 3.2.1.52; TSD; Beta-hexosaminidase subunit alpha; Hexosaminidase subunit A
应用说明
应用建议
应用推荐稀释比
FACSAssay-dependent
WB1:3000
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Purification with Protein A.
缓冲液PBS (pH 7.4), 0.02% Sodium azide and 10% Glycerol.
抗菌剂0.02% Sodium azide
稳定剂10% Glycerol
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. 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: 3073 Human HEXA

Swiss-port # P06865 Human Beta-hexosaminidase subunit alpha

基因名称HEXA
全名hexosaminidase A (alpha polypeptide)
背景介绍This gene encodes the alpha subunit of the lysosomal enzyme beta-hexosaminidase that, together with the cofactor GM2 activator protein, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Beta-hexosaminidase is composed of two subunits, alpha and beta, which are encoded by separate genes. Both beta-hexosaminidase alpha and beta subunits are members of family 20 of glycosyl hydrolases. Mutations in the alpha or beta subunit genes lead to an accumulation of GM2 ganglioside in neurons and neurodegenerative disorders termed the GM2 gangliosidoses. Alpha subunit gene mutations lead to Tay-Sachs disease (GM2-gangliosidosis type I). [provided by RefSeq, Jul 2009]
生物功能Responsible for the degradation of GM2 gangliosides, and a variety of other molecules containing terminal N-acetyl hexosamines, in the brain and other tissues. The form B is active against certain oligosaccharides. The form S has no measurable activity. [UniProt]
预测分子量61 kDa
翻译后修饰N-linked glycan at Asn-115 consists of Man(3)-GlcNAc(2).
检测图片 (3)
  • ARG57022 anti-HEXA antibody [20F1] FACS image

    Flow Cytometry: A549 cell line stained with ARG57022 anti-HEXA antibody [20F1] at 2-5 µg for 1x10^6 cells (red line). Secondary antibody: Goat anti-Mouse IgG Alexa fluor 488 conjugate. Isotype control antibody was Mouse IgG (black line).

  • ARG57022 anti-HEXA antibody [20F1] WB image

    Western blot: 40 µg of MCF7 cell lysate stained with ARG57022 anti-HEXA antibody [20F1] at 1:3000.

  • ARG57022 anti-HEXA antibody [20F1] WB image

    Western blot: 10 µg of 1) 293T cell lysate, 2) HEXA Transfected 293T cell lysate stained with ARG57022 anti-HEXA antibody [20F1] at 1:3000.

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