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AARS1 Rabbit Polyclonal Antibody

Alanine--tRNA ligase,cytoplasmic,Alanyl-tRNA synthetase (AlaRS),Protein lactyltransferase AARS1,Renal carcinoma antigen NY-REN-42,AARS

价格 600.00 供应商现货 : 3-5个工作日
货号 S0B60022
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产品介绍 评论(0)

产品规格
  • 宿主来源

    Rabbit
  • 抗原名称

    AARS1
  • 分子别名

    Alanine--tRNA ligase, cytoplasmic; Alanyl-tRNA synthetase (AlaRS); Protein lactyltransferase AARS1; Renal carcinoma antigen NY-REN-42; AARS
  • 细胞定位

    Cytoplasm, Nucleus
  • Accession

    P49588
  • 抗体类型

    Polyclonal antibody
  • 抗体同种型

    IgG
  • 反应种属 ?

    Hu, Ms, Rt
  • 阳性样本

    MCF7, A549, HeLa, HepG2, Raji, NIH/3T3, C6
  • 纯化方式

    Immunogen Affinity
  • 浓度

    0.5 mg/ml
  • 标记

    Unconjugated
  • 性状

    Liquid
  • 缓冲体系

    PBS, 40% Glycerol, 0.05% BSA, 0.02% sodium azide

  • 储存条件

    12 months from date of receipt / reconstitution, -20 °C as supplied

  • 应用

    ICC ?

    WB

  • 稀释度

    应用 稀释度 推荐种属
    WB 1:1000 Hu, Ms, Rt
    ICC 1:500 Hu
背景介绍
  • AARS1 (Alanyl-tRNA synthetase 1) is a highly evolutionarily conserved class II aminoacyl-tRNA synthetase, whose core function is to catalyze the ligation of alanine to its corresponding tRNA(Ala), thereby providing critical quality control for protein synthesis. This enzyme accomplishes its task through a two-step process: first, it activates alanine using ATP to form alanyl-AMP; second, it transfers the activated alanine to tRNA (Ala). To ensure absolute translational fidelity, AARS1 is also equipped with a built-in editing or proofreading domain, which hydrolyzes and corrects mischarged amino acids, thus preventing the synthesis of toxic proteins caused by errors in genetic information translation. Although AARS1 is widely expressed throughout the body and primarily localizes to the cytoplasm, its dysfunction exhibits remarkable tissue specificity—particularly within the nervous system, where mutations in this gene have been definitively linked to several severe neurodegenerative diseases, such as Charcot-Marie-Tooth disease (CMT2N) and developmental epileptic encephalopathy (DEE29).

  • 免疫印迹

    • WB result of AARS1 Rabbit pAb
      Primary antibody: AARS1 Rabbit pAb at 1/1000 dilution
      Lane 1: MCF7 whole cell lysate 20 µg
      Lane 2: A549 whole cell lysate 20 µg
      Secondary antibody: Goat Anti- rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 107 kDa
      Observed MW: 110 kDa

    • WB result of AARS1 Rabbit pAb
      Primary antibody: AARS1 Rabbit pAb at 1/1000 dilution
      Lane 1: NIH/3T3 whole cell lysate 20 µg
      Secondary antibody: Goat Anti- rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 107 kDa
      Observed MW: 110 kDa

    • WB result of AARS1 Rabbit pAb
      Primary antibody: AARS1 Rabbit pAb at 1/1000 dilution
      Lane 1: C6 whole cell lysate 20 µg
      Secondary antibody: Goat Anti- rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 107 kDa
      Observed MW: 110 kDa

  • 免疫细胞化学

    • ICC shows positive staining in HeLa cells. Anti-AARS1 antibody was used at 1/500 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. The cells were fixed with 100% ice-cold methanol and permeabilized with 0.1% PBS-Triton X-100. Nuclei were counterstained with DAPI (Blue). Counterstain with tubulin (Red).

    • ICC shows positive staining in HepG2 cells. Anti-AARS1 antibody was used at 1/500 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. The cells were fixed with 100% ice-cold methanol and permeabilized with 0.1% PBS-Triton X-100. Nuclei were counterstained with DAPI (Blue). Counterstain with tubulin (Red).

    • ICC shows positive staining in Raji cells. Anti-AARS1 antibody was used at 1/500 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. The cells were fixed with 100% ice-cold methanol and permeabilized with 0.1% PBS-Triton X-100. Nuclei were counterstained with DAPI (Blue). Counterstain with tubulin (Red).

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