The results of realtime RTPCR proved the accuracy of the gene chip.
经实时荧光定量逆转录聚合酶链反应验证了基因芯片准确可靠。
Semiquantitative RTPCR was used for verification of HDAC1 gene expression.
以半定量RT-PCR法检测瘤细胞中HDAC1基因表达加以验证。
Conclusion Monitoring of the WT1 gene by Nest RTPCR would be a surely marker for the detection of minimal residual disease (MRD) in acute leukemia.
结论用Nest、RT - PCR测定WT 1基因的表达可作为检测白血病微小残留病(MRD)的一项指标。
The collagen deposition, MMP2 activity and RECK expression in the liver tissues were detected by Sirius red staining, zymography and RTPCR respectively.
采用天狼猩红染色判断肝纤维化程度，明胶酶谱法检测肝组织MMP2的活性，RTPCR法检测RECK基因的表达情况。
Aim and Methods: To study the effect of ventricular fibroblasts increase beating rate on cultured neonatal rat cardiomyocytes by using cell culture and RTPCR technique.
目的和方法：利用细胞培养和RT P CR技术研究新生大鼠心脏成纤维细胞增加心肌细胞搏动频率的作用。
Methods: CEA mRNA expression in bone marrow of rib was detected in 43 patients with esophageal carcinoma and 17 patients with esophageal benign lesions as controls by RTPCR.
方法：以癌胚抗原(CEA)为分子标记物，采用RTPCR技术检测43例食管癌患者及17例食管良性病变患者肋骨骨髓中癌胚抗原的表达。
After treated for 21 d, the mice were sacrificed and liver metastasis rate and liver metastasis nodule Numbers were observed. Expression of CD gene in liver metastasis tissues was determined by RTPCR.
治疗21d后处死裸鼠，观察肝脏转移率和转移结节数，RTPCR检测CD基因在肿瘤组织的表达，光镜及电镜下观察肿瘤病理学的变化。
After treated for 21 d, the mice were sacrificed and liver metastasis rate and liver metastasis nodule Numbers were observed. Expression of CD gene in liver metastasis tissues was determined by RTPCR.
治疗21d后处死裸鼠，观察肝脏转移率和转移结节数，RTPCR检测CD基因在肿瘤组织的表达，光镜及电镜下观察肿瘤病理学的变化。
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