Methods PCR method was applied to detect the KDR mutation of the target site (sodium channel) gene.
方法采用聚合酶链反应(PCR)方法，用自行设计的特异引物，对昆虫的钠离子通道基因进行扩增。
This paper reviews the current progress of the relationship between Kdr - type resistance and sodium channel.
综述了击倒抗性与钠离子通道关系的研究进展。
The cell surface markers(CD31, CD34 and KDR) were detected by FACS analysis at differentiation 4-7 days in cell culture.
第4天到第7天，应用流式细胞仪动态检测粘附细胞表面标志CD34、CD31、KDR。
AIM: to explore the expression of vascular endothelial growth factor receptor (VEGFR) KDR and its relation with microvessel density (MVD).
前言：目的：研究骨肉瘤中血管内皮生长因子受体(VEG FR 2)KDR的表达情况，及其与微血管密度(MVD)关系。
Toxicological and electrophysiological studies have demonstrated the presence of Kdr-type resistance in many pyrethroid-resistant insects.
毒理学和电生理学的研究表明，在许多拟除虫菊酯类杀虫剂抗性昆虫中存在击倒抗性。
Conclusion: the peptide P5 that home to KDR expressed on tumor vasculature may also be useful in targeting therapies specifically to tumors.
结论：化学合成的小肽p5有望作为先导分子，在以KDR为靶点的肿瘤靶向治疗中得到应用。
Anti-KDR McAb(3G9) was used to measure the expression of KDR (kinase insert domain-containing receptor) in T24 cells and tumor tissue by immunofluorescence and immunohistochemistry.
使用抗KDR单克隆抗体（3G9），通过免疫荧光、免疫组化检测KDR在T24细胞及瘤体中的表达；
Anti-KDR McAb(3G9) was used to measure the expression of KDR (kinase insert domain-containing receptor) in T24 cells and tumor tissue by immunofluorescence and immunohistochemistry.
使用抗KDR单克隆抗体（3G9），通过免疫荧光、免疫组化检测KDR在T24细胞及瘤体中的表达；
应用推荐