用免疫共沉淀的方法鉴定E4B 的相互作用蛋白质。
Co-immunoprecipitation was used to identify the interactive protein.
必须选择适合免疫共沉淀抗体识别目的蛋白表位的细胞裂解条件。
The choice of lysis conditions must be tailored to the nature of the epitope recognized by the immunoprecipitating antibody.
免疫共沉淀法检测核蛋白中BAG-1与糖皮质激素受体（GR）的相互结合；
The interactions between BAG-1 and glucocorticoid receptor(GR)were detected with immune co-precipitation.
目的探讨免疫共沉淀法在肿瘤异质性蛋白质分子机制研究中的可行性，为肿瘤异质性研究建立一种新的方法。
Objective To explore a novel methodology for tumor heterogeneity research, we reveal the feasibility of using co immunoprecipitation in the protein molecular mechanism of tumor heterogeneity.
方法：以TRF1抗体应用免疫共沉淀方法，从细胞蛋白抽提物中分离TRF1蛋白复合物，并作蛋白质肽指纹谱鉴定；
Methods: The co immunoprecipitation assay was employed to isolate TRF1 protein complex and the immunoprecipitate was subjected to MALDI TOF mass spectrometry for protein identification.
在HEK293T细胞中，通过双荧光报告系统检测E4B对TLR信号通路的影响，并且用免疫共沉淀的方法鉴定E4B的相互作用蛋白质。
In HEK293T, Dual-Luciferase Reporter Assay System was used to evaluate the effect of E4B on TLR pathway, and co-immunoprecipitation was used to identify interactive protein.
在HEK293T细胞中，通过双荧光报告系统检测E4B对TLR信号通路的影响，并且用免疫共沉淀的方法鉴定E4B的相互作用蛋白质。
In HEK293T, Dual-Luciferase Reporter Assay System was used to evaluate the effect of E4B on TLR pathway, and co-immunoprecipitation was used to identify interactive protein.
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