WB | 咨询技术 | Human,Mouse,Rat |
IF | 咨询技术 | Human,Mouse,Rat |
IHC | 咨询技术 | Human,Mouse,Rat |
ICC | 技术咨询 | Human,Mouse,Rat |
FCM | 咨询技术 | Human,Mouse,Rat |
Elisa | 咨询技术 | Human,Mouse,Rat |
Aliases | bHLHe76 |
Entrez GeneID | 196; |
WB Predicted band size | 90kDa |
Host/Isotype | Rabbit IgG |
Antibody Type | Primary antibody |
Storage | Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles. |
Species Reactivity | Human,Mouse,Rat |
Immunogen | Peptide sequence around phosphorylation site of Serine 36 (N-P-S(p)-K-R) derived from Human AhR. |
Formulation | Purified antibody in PBS with 0.05% sodium azide. |
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以下是关于AhR (Phospho-Ser36)抗体的3篇参考文献的简要整理(注:因文献检索范围限制,部分内容可能为模拟示例,建议进一步核实):
1. **文献名称**:*Phosphorylation of Aryl Hydrocarbon Receptor (AhR) at Serine 36 Modulates Its Interaction with HSP90 and Proteasomal Degradation*
**作者**:Smith J, et al.
**摘要**:本研究通过质谱分析鉴定了AhR在Ser36位点的磷酸化修饰,开发了特异性抗体验证其磷酸化状态,并证明该修饰通过削弱AhR与HSP90的结合促进其泛素化降解。
2. **文献名称**:*AhR Phosphorylation at Ser36 Mediates Cytosolic Retention and Suppression of Inflammatory Signaling*
**作者**:Lee S, Kim M.
**摘要**:利用Phospho-Ser36特异性抗体,作者发现LPS刺激下AhR的Ser36磷酸化抑制其核转位,从而下调NF-κB通路活性,揭示其在炎症反应中的负调控作用。
3. **文献名称**:*Development of a Phospho-Specific AhR Antibody for Studying Environmental Toxin-Induced Activation*
**作者**:Brown K, et al.
**摘要**:本文报道了一种针对AhR Ser36磷酸化位点的多克隆抗体制备方法,验证其在Western blot和免疫荧光中的特异性,应用于二噁英处理后AhR激活机制的研究。
**提示**:以上文献为示例性质,实际引用时建议通过PubMed或Web of Science以关键词“AhR Ser36 phosphorylation antibody”检索近年研究,并优先选择高影响力期刊(如*JBC*、*PNAS*)的论文。部分关键研究可能集中于AhR的经典激活通路(如核转位与ARNT结合),需结合具体实验背景筛选。
The aryl hydrocarbon receptor (AhR) is a ligand-activated transcription factor that plays a central role in regulating cellular responses to environmental contaminants, such as polycyclic aromatic hydrocarbons and dioxins. Upon ligand binding, AhR translocates to the nucleus, dimerizes with ARNT, and activates genes involved in xenobiotic metabolism (e.g., CYP1A1) and immune modulation. Post-translational modifications, including phosphorylation, tightly regulate AhR activity, stability, and subcellular localization.
Phosphorylation at Serine 36 (Ser36) is a critical regulatory event in AhR signaling. This modification occurs in the N-terminal PAS domain and has been implicated in modulating AhR nuclear translocation, protein-protein interactions, and transcriptional activity. Studies suggest that phosphorylation at Ser36 may influence AhR’s response to ligands or cellular stress, affecting downstream pathways linked to inflammation, apoptosis, and carcinogenesis.
The AhR (Phospho-Ser36) antibody is a specialized tool designed to detect AhR specifically phosphorylated at Ser36. It is widely used in techniques like Western blotting, immunofluorescence, and immunoprecipitation to study AhR activation dynamics, ligand-dependent signaling, and cross-talk with other pathways (e.g., NF-κB or EGFR). Researchers employ this antibody to explore AhR’s role in toxicology, cancer biology, and immune regulation, particularly in contexts where environmental pollutants or endogenous metabolites dysregulate AhR-mediated processes. Validation in multiple species (human, mouse, rat) ensures broad applicability in preclinical and mechanistic studies.
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