WB | 1/1000 | 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 | Cyclin-dependent kinase 20, CDK-activating kinase p42, CAK-kinase p42, Cell cycle-related kinase, Cell division protein kinase 20, Cyclin-dependent protein kinase H, Cyclin-kinase-activating kinase p42, CDK20, CCRK, CDCH |
Entrez GeneID | 23552 |
WB Predicted band size | 38.7kDa |
Host/Isotype | Mouse IgG1 |
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 | Purified His-tagged CCRK protein was used to produced this monoclonal antibody. |
Formulation | Purified antibody in TBS with 0.05% sodium azide. |
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以下是关于CCRK (N-term)抗体的假设性参考文献示例(基于常见研究方向推测,实际文献可能需要进一步检索):
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1. **文献名称**:*"Characterization of a Novel N-terminal Specific Antibody for CCRK in Hepatocellular Carcinoma"*
**作者**:Li, X., Zhang, Y., & Wang, Q.
**摘要**:本研究开发并验证了一种针对CCRK蛋白N端表位的高特异性抗体,应用于肝细胞癌(HCC)组织样本的免疫组化分析,发现CCRK表达水平与肿瘤进展显著相关。
2. **文献名称**:*"CCRK Promotes Cell Cycle Progression via N-terminal Domain Interaction with Cyclin-Dependent Kinases"*
**作者**:Chen, J., Liu, R., & Sun, M.
**摘要**:通过使用N端特异性抗体进行免疫共沉淀(Co-IP)实验,揭示了CCRK通过其N端结构域与CDK2/4结合,调控G1/S期转换的分子机制。
3. **文献名称**:*"Development and Validation of a CCRK N-terminal Antibody for Functional Studies in Pancreatic Cancer"*
**作者**:Gupta, S., Patel, T., & Kim, H.
**摘要**:报道了一种兔源多克隆抗体的开发流程,该抗体针对CCRK的N端抗原表位,成功用于胰腺癌细胞系的Western blot和流式细胞术检测,并验证了其在靶向治疗研究中的应用潜力。
4. **文献名称**:*"CCRK N-terminal Epitope-Specific Antibody Reveals Its Role in TGF-β Signaling Pathway"*
**作者**:Zhang, L., Wu, F., & Zhou, D.
**摘要**:利用N端特异性抗体阻断实验,证明CCRK通过N端结构域参与TGF-β/Smad信号通路的激活,为靶向干预提供了实验依据。
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**注意**:以上文献为模拟示例,实际研究中需通过PubMed、Google Scholar等平台以关键词“CCRK antibody N-terminal”或“CDK20 antibody”检索真实文献。若研究领域较新,可扩展至CCRK功能研究论文,并参考其“Methods”部分中抗体使用描述。
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