anti-ACY1 / Aminoacylase 1 antibody [1E2]

Key features and details

  • 产品描述: Mouse Monoclonal antibody [1E2] recognizes ACY1 / Aminoacylase 1
  • 反应物种: Hu
  • 应用: FACS, WB
  • 宿主: Mouse
  • 克隆: Monoclonal
  • 克隆号: 1E2
  • 同位型: IgG2b, kappa
  • 靶点名称: ACY1 / Aminoacylase 1
  • 抗原物种: Human
  • Brand:
CAT.NO. : ARG57036
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Product Details
概述
产品描述Mouse Monoclonal antibody [1E2] recognizes ACY1 / Aminoacylase 1
反应物种Hu
应用FACS, WB
宿主Mouse
克隆Monoclonal
克隆号1E2
同位型IgG2b, kappa
靶点名称ACY1 / Aminoacylase 1
抗原物种Human
抗原Recombinant fragment around aa. 1-408 of Human Aminoacylase 1.
偶联标记Un-conjugated
別名ACY-1; N-acyl-L-amino-acid amidohydrolase; ACY1D; EC 3.5.1.14; HEL-S-5; Aminoacylase-1
应用说明
应用建议
应用推荐稀释比
FACSAssay-dependent
WB1:250 - 1:500
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: 95 Human ACY1

Swiss-port # Q03154 Human Aminoacylase-1

基因名称ACY1
全名aminoacylase 1
背景介绍This gene encodes a cytosolic, homodimeric, zinc-binding enzyme that catalyzes the hydrolysis of acylated L-amino acids to L-amino acids and an acyl group, and has been postulated to function in the catabolism and salvage of acylated amino acids. This gene is located on chromosome 3p21.1, a region reduced to homozygosity in small-cell lung cancer (SCLC), and its expression has been reported to be reduced or undetectable in SCLC cell lines and tumors. The amino acid sequence of human aminoacylase-1 is highly homologous to the porcine counterpart, and this enzyme is the first member of a new family of zinc-binding enzymes. Mutations in this gene cause aminoacylase-1 deficiency, a metabolic disorder characterized by central nervous system defects and increased urinary excretion of N-acetylated amino acids. Alternative splicing of this gene results in multiple transcript variants. Read-through transcription also exists between this gene and the upstream ABHD14A (abhydrolase domain containing 14A) gene, as represented in GeneID:100526760. A related pseudogene has been identified on chromosome 18. [provided by RefSeq, Nov 2010]
生物功能Involved in the hydrolysis of N-acylated or N-acetylated amino acids (except L-aspartate). [UniProt]
预测分子量46 kDa
检测图片 (3)
  • ARG57036 anti-ACY1 / Aminoacylase 1 antibody [1E2] FACS image

    Flow Cytometry: Hep3B cells stained with ARG57036 anti-ACY1 / Aminoacylase 1 antibody [1E2] at 2-5 µg/10^6 cells (red line). Secondary antibody: Goat anti-Mouse IgG Alexa fluor 488 conjugate. Isotype control antibody was Mouse IgG (black line).

  • ARG57036 anti-ACY1 / Aminoacylase 1 antibody [1E2] WB image

    Western blot: 40 µg of Jurkat, HepG2, HeLa, and A549 stained with ARG57036 anti-ACY1 / Aminoacylase 1 antibody [1E2] at 1:500.

  • ARG57036 anti-ACY1 / Aminoacylase 1 antibody [1E2] WB image

    Western blot: 50 ng of Recombinant Human ACY1 stained with ARG57036 anti-ACY1 / Aminoacylase 1 antibody [1E2] at 1:1000.

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