Apoptosis was detected by flow cytometric analysis.
用流式细胞仪观察细胞凋亡。
Peripheral t - lymphocyte subsets and NK cells were examined by flow cytometric analysis.
应用流式细胞法检测所有研t淋巴细胞亚群和NK细胞。
Flow cytometric analysis of MKN-45 cells, untreated (green) or treated with SU11274 (blue).
对MKN - 45细胞进行流式细胞术检测：未处理的(绿色)，SU11274处理的(蓝色)。
The changes in cell cycle progression of synchronized HUVECs were examined by flow cytometric analysis.
用流式细胞技术检测各组细胞周期，观察细胞增殖能力的变化。
The DNA contents and cells periods in 16 resected epileptic focuses were determined by Flow Cytometric Analysis.
提要本文报告用流式细胞仪测定16例不同癫痫病灶中DNA含量和细胞周期的变化情况。
Flow cytometric analysis of K562 cells using c-Rel antibody (blue) compared to a nonspecific negative control antibody (red).
流式细胞仪研究K562细胞，所用抗体为c - RelAntibody(蓝色)与非特异性的阴性对照抗体(红色)。
Flow cytometric analysis revealed that NGF treatment increased the number of EPCs in the peripheral circulation of C57BL/6 mice.
流式细胞分析显示神经生长因子处理后能够增加C57BL/6小鼠外周循环系统中的内皮祖细胞数量急剧增加。
Flow cytometric analysis of MCF-7 cells, using MUC1 (VU4H5) Mouse mAb (blue) compared to a nonspecifc negative control antibody (red).
使用MUC1 （VU4H5）鼠单抗（蓝色）对MCF-7细胞进行流式分析，对照使用阴性对照抗体（红色）。
Flow cytometric analysis of A-204 cells using Numb (C29G11) Rabbit mAb (blue) compared to a nonspecific negative control antibody (red).
使用Numb (C29G11)兔单抗(蓝色)对A- 204细胞进行流式细胞分析，对照使用阴性对照抗体(红色)。
Flow cytometric analysis of C2C12 cells using HSP27 Antibody (Rodent Preferred) (blue) compared to a nonspecific negative control antibody (red).
使用HSP27抗体（啮齿类偏好）（蓝）和非特异的阴性对照抗体（红），对C2C12细胞进行流式细胞仪分析。
Method:The peripheral blood lymphocyte subsets were examined in 30 patients with lung cancer before and after operation by flow cytometric analysis.
方法：用流式细胞仪检测30例根治切除的肺癌患者术前、术后不同时期外周血淋巴细胞亚群中各种细胞因子。
Flow cytometric analysis of unpermeabilized HT-29 cells using EpCAM (VU1D9) Mouse mAb (blue) compared to a nonspecific negative control antibody (red).
使用EpCAM（VU1D9）小鼠单抗（蓝色）对比非特异性对照抗体（红色）对非渗透性HT-29细胞进行流式细胞分析。
Methods:By checking the morphology of apoptotic cells, agarose gel electrophoresis of DNA fragmentation and quantitation of apoptotic cells by means of flow cytometric analysis.
方法：应用细胞形态学检查，DNA凝胶电泳及流式细胞仪分析检测。
Using DNA gel electrophoresis, electron microscopic examination and flow cytometric analysis, program cell death induced by hyperthermia in mouse G422 glioma in vivo was studied.
应用DNA凝胶电冰、电镜观察和流式细胞仪分析，对加热诱导G422胶质瘤程序性细胞死亡的作用进行了研究。
Methods: After establishing a C6/SD glioma model, by using flow cytometric analysis, immunohistochemistry and HE stain three methods, the proliferation kinetics in C6 glioma cell was measured.
方法：建立C6/SD大鼠胶质瘤模型后，应用流式细胞仪检测、免疫组化、HE染色三种方法，研究C6胶质瘤细胞的增殖动力学指标。
TPOFF results were similar to both flow-cytometric analysis of tumor cells after isolation and suspension, and fluorescence determined by microscope images of cryo sectioned tumors.
TPOFF检查结果不但与分离并悬浮后的肿瘤细胞流式细胞检测分析的结果类似，也与肿瘤冰冻切片的荧光显微成像一致。
Researches have shown that flow cytometric DNA analysis can detect DNA aneuploidy in as much as 92% of tumors.
研究显示，流式细胞术DNA倍体分析可以在92 %的实体肿瘤上检测到DNA异倍体的存在。
Researches have shown that flow cytometric DNA analysis can detect DNA aneuploidy in as much as 92% of tumors.
研究显示，流式细胞术DNA倍体分析可以在92 %的实体肿瘤上检测到DNA异倍体的存在。
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