WB | DB: 1/500 | 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 | Inhibitor of nuclear factor kappa-B kinase subunit beta, I-kappa-B-kinase beta, IKK-B, IKK-beta, IkBKB, I-kappa-B kinase 2, IKK2, Nuclear factor NF-kappa-B inhibitor kinase beta, NFKBIKB, IKBKB, IKKB |
Entrez GeneID | 3551 |
WB Predicted band size | 86.6kDa |
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 | This IKKB Antibody is generated from rabbits immunized with a KLH conjugated synthetic phosphopeptide corresponding to amino acid residues surrounding S689 of human IKKB. |
Formulation | Purified antibody in PBS with 0.05% sodium azide. |
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以下是关于Phospho-IKKβ (S689)抗体的参考文献示例(部分内容为假设性概括,具体文献需根据实际研究验证):
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1. **"IKKβ phosphorylation at Serine 689 regulates NF-κB activation in response to TNF-α"**
*Authors: Lee et al. (2015)*
**摘要**:研究揭示了IKKβ在Serine 689位点的磷酸化对TNF-α诱导的NF-κB信号通路的激活至关重要。作者通过突变实验和Phospho-IKKβ(S689)抗体检测,证明该位点的磷酸化增强了IKK复合物的激酶活性,促进炎症反应。
2. **"A novel phosphorylation site in IKKβ modulates oxidative stress-induced cell death"**
*Authors: Zhang et al. (2018)*
**摘要**:本文发现IKKβ的Serine 689磷酸化在氧化应激条件下被特异性激活,通过Phospho-IKKβ(S689)抗体检测证实其与细胞凋亡相关。抑制该位点磷酸化可减少ROS介导的细胞损伤,提示其作为潜在治疗靶点。
3. **"Phosphorylation of IKKβ at S689 mediates crosstalk between PI3K/Akt and NF-κB pathways"**
*Authors: Chen et al. (2020)*
**摘要**:研究利用Phospho-IKKβ(S689)抗体证实,PI3K/Akt通路通过磷酸化IKKβ的S689位点调控NF-κB的转录活性,促进肿瘤细胞的生存和迁移,为癌症治疗提供了新机制。
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**注**:以上文献为示例,实际研究中IKKβ更常见的磷酸化位点为S177/S181(激活位点)。若需准确文献,请通过PubMed或Google Scholar检索关键词“Phospho-IKKβ Ser689”或联系抗体供应商提供的引用文献。
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