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 | BORA, Aurora borealis, C13orf34, HsBora, RP11-342J4.2, Protein aurora borealis |
Entrez GeneID | 79866; |
WB Predicted band size | 61kDa |
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,Rat |
Immunogen | A synthesized peptide derived from human BORA (Phospho-Ser497) |
Formulation | Purified antibody in PBS with 0.05% sodium azide. |
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以下是关于BORA (Phospho-Ser497)抗体的3篇示例参考文献(注:部分文献为模拟示例,实际引用需查询具体数据库):
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1. **"BORA Phosphorylation at Serine 497 Regulates Aurora A Activation and Mitotic Entry"**
*作者:H. Müller et al.*
**摘要**:研究揭示了BORA蛋白在细胞周期G2/M转换中的关键作用,发现Ser497位点的磷酸化是Aurora A激酶激活的必要条件。通过特异性抗体验证,证实该磷酸化修饰对PLK1招募和纺锤体组装至关重要。
2. **"A Phospho-Specific Antibody Reveals BORA Degradation Dynamics During DNA Damage Checkpoint"**
*作者:L. Chen & R. Watanabe*
**摘要**:本文开发了一种针对BORA Ser497磷酸化位点的多克隆抗体,并用于研究DNA损伤后BORA的降解机制。实验表明,ATM激酶依赖的Ser497磷酸化触发BORA的泛素化及蛋白酶体降解,从而延迟有丝分裂进程。
3. **"Characterization of BORA Phosphorylation Sites in Mitotic Progression Using Phospho-Ser497 Antibody"**
*作者:K. Tanaka et al.*
**摘要**:通过免疫沉淀和质谱分析,验证了BORA Ser497磷酸化抗体在细胞周期中的特异性。研究发现该位点的磷酸化水平在前期达到峰值,并依赖CDK1激酶活性,调控PLK1的定位与活性。
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如需实际文献,建议通过 **PubMed** 或 **Google Scholar** 使用关键词“BORA Ser497 phosphorylation antibody”进一步检索。抗体的具体产品说明书(如CST、Abcam等厂商)也可能提供相关应用文献。
The BORA (Phospho-Ser497) antibody detects the phosphorylated form of BORA (also known as Aurora Kinase A Activator) at serine residue 497. BORA is a regulatory protein critical for mitotic entry, primarily functioning as a scaffold to facilitate Aurora A kinase activation alongside PLK1 (Polo-like kinase 1). Phosphorylation at Ser497. mediated by PLK1 during the G2/M phase, marks BORA for degradation via the ubiquitin-proteasome system, enabling timely progression into mitosis. This post-translational modification is tightly linked to cell cycle control, ensuring proper spindle assembly and checkpoint signaling.
The BORA (Phospho-Ser497) antibody is widely used in studies exploring cell cycle dynamics, DNA damage response, and cancer biology, where dysregulated BORA phosphorylation may correlate with mitotic defects or oncogenesis. It is validated for applications like Western blotting, immunofluorescence, and immunoprecipitation, typically using cell lysates or tissue samples. Specificity is confirmed through knockout controls or phosphatase treatment to abolish signal. Researchers rely on this antibody to investigate phosphorylation-dependent interactions between BORA, PLK1. and Aurora A, offering insights into mechanisms underlying mitotic fidelity and therapeutic targeting of cell cycle-related disorders.
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