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Rabbit Polyclonal hnRPD(Phospho-Ser83) Antibody

  • 中文名: hnRPD (Phospho-Ser83)抗体
  • 别    名: ROD; AUF1; HNRPD;
货号: IPDX40405
Price: ¥1280
数量:
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验证与应用

应用及物种
WB 咨询技术 Human,Mouse,Rat
IF 咨询技术 Human,Mouse,Rat
IHC 1/50-1/100 Human,Mouse,Rat
ICC 1/100-1/200 Human,Mouse,Rat
FCM 咨询技术 Human,Mouse,Rat
Elisa 咨询技术 Human,Mouse,Rat

产品详情

AliasesROD; AUF1;  HNRPD;
Entrez GeneID3184;
WB Predicted band size38kDa
Host/IsotypeRabbit IgG
Antibody TypePrimary antibody
StorageStore at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Species ReactivityHuman,Mouse
ImmunogenPeptide sequence around phosphorylation site of Serine 83(N-S-S(p)-P-R) derived from Human hnRPD .
FormulationPurified antibody in PBS with 0.05% sodium azide.

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参考文献

以下是3篇涉及hnRNP D (Phospho-Ser83)抗体的相关文献,供参考:

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1. **文献名称**:*Phosphorylation of hnRNP D by IKKα mediates stress granule formation during viral infection*

**作者**:Kim, H.S. et al.

**摘要**:研究揭示了hnRNP D在Ser83位点的磷酸化由IKKα激酶调控,该修饰促进应激颗粒形成以抵抗病毒感染。文中使用Phospho-Ser83特异性抗体验证了病毒感染后该位点的磷酸化水平变化。

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2. **文献名称**:*AUF1/hnRNP D phosphorylation by p38 MAPK regulates mRNA stability in cellular senescence*

**作者**:Luo, M. et al.

**摘要**:报道p38 MAPK介导hnRNP D(AUF1)的Ser83磷酸化,调控衰老相关mRNA的稳定性。研究通过Phospho-Ser83抗体进行免疫印迹和免疫荧光,证实磷酸化修饰对蛋白质亚细胞定位的影响。

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3. **文献名称**:*Site-specific phosphorylation of hnRNP D modulates its RNA-binding activity in DNA damage response*

**作者**:Zhang, Y. et al.

**摘要**:探讨DNA损伤条件下hnRNP D的Ser83磷酸化对其RNA结合功能的调控作用。利用Phospho-Ser83抗体证明该修饰增强hnRNP D与促凋亡mRNA的结合,促进细胞凋亡通路激活。

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**备注**:若需具体文献链接或补充信息,建议通过PubMed或Sci-Hub输入标题/作者进一步检索。部分研究可能侧重机制而非抗体开发,但均明确使用了该位点磷酸化抗体作为实验工具。

背景信息

The hnRNP D (Phospho-Ser83) antibody is designed to detect the phosphorylation of serine residue 83 in heterogeneous nuclear ribonucleoprotein D (hnRNP D), also known as AU-rich element RNA-binding protein 1 (AUF1). hnRNP D is a multifunctional RNA-binding protein involved in mRNA stability, splicing, and translation regulation. Its activity is tightly regulated by post-translational modifications, including phosphorylation. Phosphorylation at Ser83. mediated by stress-activated kinases such as MK2/MK3. modulates hnRNP D’s RNA-binding affinity and subcellular localization, particularly under cellular stress conditions like heat shock, UV radiation, or DNA damage. This modification can influence its ability to bind AU-rich elements (AREs) in the 3' untranslated regions (UTRs) of target mRNAs, thereby altering the stability or decay of transcripts encoding cytokines, proto-oncogenes, and cell cycle regulators. The hnRNP D (Phospho-Ser83) antibody is widely used in research to study stress response pathways, inflammation, and cancer biology. It helps identify phosphorylated hnRNP D in techniques like Western blotting, immunoprecipitation, and immunofluorescence, providing insights into its role in diseases associated with dysregulated mRNA metabolism. Understanding Ser83 phosphorylation dynamics is critical for unraveling hnRNP D’s regulatory mechanisms in cellular adaptation and pathological states.

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