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。
Methods: The localization and distribution of VEGF and its receptor KDR in 47 cases of PGC were detected by immunohistochemistry LDP method.
方法：采用免疫组织化学ldp法研究47例PG C组织中vegf及其受体(KDR)的定位与表达。
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。
Conclusion KDR promoter may regulate the CDglyTK fusion gene system to selectively kill the KDR-expressing SCG7901 cells and to induce the cell apoptosis.
结论KD R启动子可以调控融合基因体系选择性地杀伤人胃癌scg7901细胞，并且该体系可以诱导胃癌细胞凋亡。
Conclusions the double suicide gene driven by KDR promoter has specific killing effect on KDR-expressing gastric tumor cells and venous endothelial cells in vitro.
结论KDR基因启动子可调控双自杀基因系统选择性杀伤表达KDR胃癌细胞及血管内皮细胞。
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；
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