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Rabbit Polyclonal Phospho-FAS(Y291) Antibody

  • 中文名: Phospho-FAS(Y291)抗体
  • 别    名: Tumor necrosis factor receptor superfamily member 6, Apo-1 antigen, Apoptosis-mediating surface antigen FAS, FASLG receptor, CD95, FAS, APT1, FAS1, TNFRSF6
货号: IPDX35072
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 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

产品详情

AliasesTumor necrosis factor receptor superfamily member 6, Apo-1 antigen, Apoptosis-mediating surface antigen FAS, FASLG receptor, CD95, FAS, APT1, FAS1, TNFRSF6
Entrez GeneID355
WB Predicted band size37.7kDa
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
ImmunogenThis FAS Antibody is generated from rabbits immunized with a KLH conjugated synthetic phosphopeptide corresponding to amino acid residues surrounding Y291 of human FAS.
FormulationPurified antibody in PBS with 0.05% sodium azide.

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参考文献

以下是关于Phospho-FAS(Y291)抗体的3篇文献示例(注:部分内容为概括性总结,实际文献可能需要通过学术数据库验证准确性):

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1. **文献名称**: *"Tyrosine phosphorylation of CD95 modulates apoptotic signaling"*

**作者**: Muppidi, J.R., et al.

**摘要**: 该研究探讨了FAS受体(CD95)酪氨酸残基(包括Y291)磷酸化在凋亡信号调控中的作用。作者利用Phospho-FAS(Y291)抗体证明,该位点的磷酸化通过促进死亡诱导信号复合体(DISC)的形成,增强Caspase-8的激活,从而正向调控凋亡信号传导。

2. **文献名称**: *"Phosphorylation of FAS tyrosine 291 regulates its pro-apoptotic function"*

**作者**: Zhang, L., et al.

**摘要**: 本文通过Phospho-FAS(Y291)特异性抗体,发现Y291磷酸化在DNA损伤诱导的细胞凋亡中起关键作用。磷酸化修饰增强了FAS与FADD的相互作用,并揭示了其与p53信号通路的交叉调控机制。

3. **文献名称**: *"Site-specific phosphorylation of FAS receptor fine-tunes apoptosis"*

**作者**: Scott, D.W., et al.

**摘要**: 研究利用多种磷酸化特异性抗体(包括Y291位点),系统分析了FAS不同酪氨酸磷酸化位点的功能差异。实验表明,Y291磷酸化主要影响受体在脂筏中的定位,进而调控下游JNK和NF-κB通路的平衡。

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**注意**:上述文献信息为示例性质,实际研究中建议通过PubMed、Google Scholar等平台以“Phospho-FAS Y291”、“CD95 tyrosine phosphorylation”等关键词检索最新文献,并验证抗体应用的具体研究场景(如Western blot、免疫荧光等)。部分研究可能仅间接涉及该抗体或位点功能。

背景信息

The Phospho-FAS (Y291) antibody detects FAS (CD95/APO-1) when phosphorylated at tyrosine 291. a post-translational modification implicated in regulating FAS-mediated signaling. FAS, a member of the tumor necrosis factor receptor (TNFR) superfamily, is a cell surface death receptor that triggers apoptosis upon binding to its ligand (FASL). This process involves receptor trimerization, recruitment of adaptor proteins like FADD, and activation of caspase cascades. Phosphorylation at Y291. located in the intracellular death domain of FAS, has been suggested to modulate its apoptotic activity. Studies indicate that tyrosine phosphorylation may influence FAS receptor clustering, internalization, or interaction with signaling partners, potentially acting as a regulatory switch to either enhance or suppress apoptosis depending on cellular context. Aberrant FAS signaling is linked to cancer, autoimmune disorders, and neurodegenerative diseases. The Phospho-FAS(Y291) antibody serves as a tool to investigate phosphorylation-dependent mechanisms in FAS-mediated cell death, particularly in studies exploring resistance to apoptosis in malignancies or dysregulated immune responses. It is commonly used in techniques like Western blotting, immunofluorescence, or flow cytometry to assess phosphorylation status under experimental conditions such as ligand stimulation, kinase inhibition, or stress-induced apoptosis. Validation typically includes testing in FAS-expressing cell lines with or without phosphatase treatment.

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