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AHR Recombinant Rabbit mAb (S-2370-150)

Aryl hydrocarbon receptor,Ah receptor,AhR,Class E basic helix-loop-helix protein 76 (bHLHe76),BHLHE76

价格 600.00 供应商现货 : 3-5个工作日
货号 S0B6455
规格
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产品规格
  • 宿主来源

    Rabbit
  • 抗原名称

    AHR
  • 分子别名

    Aryl hydrocarbon receptor; Ah receptor; AhR; Class E basic helix-loop-helix protein 76 (bHLHe76); BHLHE76
  • 免疫原

    Synthetic Peptide
  • 细胞定位

    Nucleus, Cytoplasm
  • Accession

    P35869
  • 克隆号

    S-2370-150
  • 抗体类型

    Recombinant mAb
  • 抗体同种型

    IgG
  • 反应种属 ?

    Hu, Ms, Rt, Mk
  • 阳性样本

    A204, HepG2, A431, MCF7, PC-3, C2C12, mouse testis, rat liver, COS-7
  • 纯化方式

    Protein A
  • 浓度

    0.5 mg/ml
  • 标记

    Unconjugated
  • 性状

    Liquid
  • 缓冲体系

    PBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300

  • 储存条件

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

  • 应用

    ChIP

    ICC ?

    WB

  • 稀释度

    应用 稀释度 推荐种属
    WB 1:1000 Hu, Ms, Rt, Mk
    ICC 1:500 Hu
    ChIP 1:20-1:50 Hu
背景介绍
  • The aryl hydrocarbon receptor (AHR) is an evolutionarily conserved, ligand-activated transcription factor that resides primarily in the cytoplasm as part of an HSP90-containing multiprotein complex; upon binding planar aromatic ligands—ranging from environmental pollutants such as dioxins and polycyclic aromatic hydrocarbons to endogenous or dietary molecules like tryptophan photoproducts and flavonoids—it translocates to the nucleus, heterodimerizes with its partner ARNT (HIF-1β), and binds xenobiotic response elements (XRE/DRE) to drive transcription of genes involved in xenobiotic metabolism (e.g., CYP1A1), but it also exerts broad non-genomic and non-canonical actions by crosstalking with NF-κB, Wnt, MAPK, and hypoxia signaling pathways, thereby modulating immune cell differentiation, inflammatory cytokine production, antioxidant responses, cell cycle checkpoints, and even osteoclastogenesis, placing AHR at the hub of environmental sensing, metabolic homeostasis, immune tolerance, and pathologies including autoimmunity, cancer, osteoporosis, and premature aging.

  • 免疫印迹

    • WB result of AHR Recombinant Rabbit mAb
      Primary antibody: AHR Recombinant Rabbit mAb at 1/1000 dilution
      Lane 1: A204 whole cell lysate 20 µg
      Lane 2: HepG2 whole cell lysate 20 µg
      Lane 3: A431 whole cell lysate 20 µg
      Lane 4: MCF7 whole cell lysate 20 µg
      Lane 5: PC-3 whole cell lysate 20 µg
      Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 96 kDa
      Observed MW: 96 kDa

    • WB result of AHR Recombinant Rabbit mAb
      Primary antibody: AHR Recombinant Rabbit mAb at 1/1000 dilution
      Lane 1: C2C12 whole cell lysate 20 µg
      Lane 2: mouse testis lysate 20 µg
      Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 96 kDa
      Observed MW: 96 kDa

    • WB result of AHR Recombinant Rabbit mAb
      Primary antibody: AHR Recombinant Rabbit mAb at 1/1000 dilution
      Lane 1: rat liver lysate 20 µg
      Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 96 kDa
      Observed MW: 96 kDa

    • WB result of AHR Recombinant Rabbit mAb
      Primary antibody: AHR Recombinant Rabbit mAb at 1/1000 dilution
      Lane 1: COS-7 whole cell lysate 20 µg
      Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 96 kDa
      Observed MW: 96 kDa

  • 免疫细胞化学

    • ICC shows positive staining in HepG2 cells. Anti-AHR 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).

  • ChIP

    • Chromatin immunoprecipitation (ChIP) was performed on HepG2 cells cross-linked with 1% formaldehyde for 10 min, then chromatin was fragmented by sonication.
      Parallel reactions used AHR Recombinant Rabbit mAb (S-2370-150) and Rabbit mAb IgG Isotype Control (SDT-R173) at 1:50 for immunoprecipitation.
      Post - immunoprecipitation, both samples were washed, eluted, and cross - links reversed. Purified DNA was analyzed by qPCR.

      qPCR showed the enrichment of CYP1A1, NFE2L2 and SAT-α in AHR Recombinant
      Rabbit mAb (S-2370-150)-immunoprecipitated sample.

FAQs

斯达特公司的抗体,可以回收利用几次?

我们一般不推荐客户回收利用抗体。 因为抗体使用之后缓冲体系已经发生改变,不同客户在回收抗体的保存条件上也会有差异,所以抗体回收使用效果无法保证。另外,我们对一批抗体回收验证测试,测试结果显示不同抗体可回收次数不同,一般效价越高的抗体,可重复使用的次数越多,客户可根据实验情况来确定

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