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 |
Aliases | G3BP; GAP SH3-domain binding protein 1; |
Entrez GeneID | 10146; |
WB Predicted band size | 60kDa |
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 |
Immunogen | Peptide sequence around phosphorylation site of serine 232 (S-S-S(p)-P-A) derived from Human G3BP-1. |
Formulation | Purified antibody in PBS with 0.05% sodium azide. |
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以下是关于G3BP-1(Phospho-Ser232)抗体的3篇文献参考,按简单格式整理:
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1. **文献名称**:*Phosphorylation of G3BP1-Ser232 facilitates stress granule formation by promoting its oligomerization*
**作者**:Zhang H, et al.
**摘要**:研究揭示了Ser232磷酸化通过增强G3BP-1寡聚化能力调控应激颗粒(stress granules)的组装,抗体用于检测该位点磷酸化水平及其在细胞应激反应中的功能。
2. **文献名称**:*G3BP1 phosphorylation-dependent stress granule dynamics regulate viral replication and innate immune signaling*
**作者**:Yang P, et al.
**摘要**:利用Phospho-Ser232抗体发现,病毒感染通过激活激酶MK2磷酸化G3BP-1.抑制应激颗粒形成以逃逸宿主抗病毒反应,揭示了其在先天免疫中的新机制。
3. **文献名称**:*A phospho-switch in G3BP1 regulates amyloid-beta aggregation and synaptic toxicity in Alzheimer’s disease*
**作者**:Lee JY, et al.
**摘要**:通过Phospho-Ser232特异性抗体证实,磷酸化G3BP-1促进神经元中Aβ聚积和突触损伤,为阿尔茨海默病病理机制提供了新治疗靶点。
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注:以上文献为虚拟示例,实际引用需根据具体研究检索PubMed或Google Scholar获取。
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