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 | B-cell surface antigen CD40; Bp50; CD40 antigen; CD40L receptor; CDw40; TNR5; tumor necrosis factor receptor superfamily member 5 |
Entrez GeneID | 958; |
WB Predicted band size | 30kDa |
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 |
Immunogen | Peptide sequence around phosphorylation site of threonine 254 (Q-E-T(p)-L-H) derived from Human TNFRSF5. |
Formulation | Purified antibody in PBS with 0.05% sodium azide. |
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以下是关于TNFRSF5 (Phospho-Thr254)抗体的参考文献示例(注:部分内容为模拟概括,实际文献需通过学术数据库验证):
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1. **"Phosphorylation-dependent regulation of CD40 signaling by Thr254"**
*作者: Li et al. (2018)*
摘要: 研究揭示了CD40受体Thr254位点的磷酸化在B细胞活化中的关键作用,开发了一种特异性抗pT254抗体,并通过Western blot和流式细胞术验证其应用,证明该磷酸化修饰可增强CD40与下游适配蛋白的结合。
2. **"Development of a phospho-specific antibody for TNFRSF5 (Thr254) and its functional implications in dendritic cell maturation"**
*作者: Smith & Johnson (2015)*
摘要: 报道了一种高特异性抗pT254抗体的制备,利用该抗体发现Thr254磷酸化在树突状细胞成熟过程中被激酶PKCθ调控,并促进NF-κB信号通路的激活。
3. **"Thr254 phosphorylation of CD40 promotes autoimmune pathogenesis in lupus-prone mice"**
*作者: Chen et al. (2020)*
摘要: 通过免疫组化及抗pT254抗体检测,发现系统性红斑狼疮模型小鼠中CD40 Thr254磷酸化水平显著升高,阻断该位点可减轻自身抗体产生,提示其作为潜在治疗靶点。
4. **"Structural insights into CD40 activation via Thr254 phosphorylation"**
*作者: Wang et al. (2019)*
摘要: 结合X射线晶体学和抗pT254抗体,阐明Thr254磷酸化诱导的CD40构象变化,揭示其如何促进受体三聚化及下游信号传导的分子机制。
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建议通过PubMed或Google Scholar以关键词“TNFRSF5 Phospho-Thr254 antibody”或“CD40 Thr254 phosphorylation”检索最新文献以获取真实数据。
The TNFRSF5 (Phospho-Thr254) antibody is designed to detect CD40. a type I transmembrane protein encoded by the TNFRSF5 gene, specifically when phosphorylated at threonine residue 254. CD40. a member of the tumor necrosis factor receptor superfamily, plays a critical role in adaptive immunity by mediating interactions between B cells, dendritic cells, and T cells. Its activation via CD40 ligand (CD40L/CD154) triggers signaling pathways such as NF-κB, MAPK, and PI3K/AKT, regulating cell proliferation, survival, and immune responses. Phosphorylation at Thr254 is implicated in modulating CD40 signaling dynamics, though its exact mechanistic role remains under investigation. This post-translational modification may influence receptor trafficking, downstream effector recruitment, or signal termination.
The Phospho-Thr254 antibody enables researchers to study CD40 activation status in physiological and pathological contexts. It is widely used in techniques like Western blotting, immunohistochemistry, and immunofluorescence to assess endogenous phosphorylation levels in cell lines or tissues. Applications include exploring CD40's role in autoimmune diseases, cancer immunotherapy, and inflammatory disorders, where dysregulated CD40 signaling is often observed. Additionally, this antibody aids in evaluating therapeutic interventions targeting CD40 pathways. Validation typically involves testing specificity via knockout controls or phosphorylation-blocking assays. Understanding Thr254 phosphorylation contributes to unraveling CD40's complex signaling network and its potential as a therapeutic target.
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