应用DNA流式细胞分析法检测17例慢性光化性皮炎的皮肤活检标本。
The skin biopsy specimens from 17 patients with chronic actinic dermatitis were estimated by DNA flow cytometry.
采用流式细胞分析法检测了低频脉冲电场对人真皮成纤维细胞细胞周期的影响。
The effect of low frequency pulsed electric field on dermal fibroblast was examined by flow cytometry analysis.
在免疫组织化学和流式细胞分析实验中，可以作为一个阻断剂，评估抗体反应的特异性。
Use as a blocking reagent to evaluate the specificity of antibody reactivity in immunohistochemistry and flow cytometry protocols.
应用同位素标记前体掺入和流式细胞分析的方法，研究CP对体外培养K 562细胞的直接作用。
The direct effect of CP on cultured K562 cells is examined in vitro by means of incorporation of isotope-labelled precursors and flow cytometry.
本文用流式细胞分析术(FCM)对35例骨巨细胞瘤(GCT)细胞核d NA含量进行了分析。
The cellular DNA contents of 35 giant cell tumors of bone (GCT) were analysed by flow cytometry (FCM).
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 revealed that NGF treatment increased the number of EPCs in the peripheral circulation of C57BL/6 mice.
二抗的最佳稀释度根据实际应用来确定。最终稀释度为1：500时，对于大多数的流式细胞分析都能得出可取的结果。
The optimal dilution of the secondary antibody should be determined for each application. However, a final dilution of 1:500 should yield acceptable results for most flow cytometry applications.
采用双标记流式细胞分析技术，分别检测各组小鼠脾脏及肠系膜淋巴结（MLN）CD80M和CD86 M的表达。
The number of CD80/CD86 M of spleen and mesenteric lymph node(MLN) were determined by double-label FCM method.
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 A-204 cells using Numb (C29G11) Rabbit 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。
Flow cytometric analysis of unpermeabilized HT-29 cells using EpCAM (VU1D9) Mouse mAb (blue) compared to a nonspecific negative control antibody (red).
通过流式细胞仪对细胞表面标记物进行免疫表型分析。
Immunophenotypic analysis of cell surface markers was performed by flow cytometry.
方法采用流式细胞术对尚未进行化疗的91例恶性肿瘤患者体腔液细胞DNA含量进行了检测和分析。
Methods DNA contents in coelom fluid cells were measured and analyzed from 91 patients with malignant carcinomas by flow cytometry.
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。
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.
方法：应用细胞形态学、流式细胞仪分析及DNA凝胶电泳等。
Method: Apoptosis was detected by the morphologic observation, flow cytometry assay and DNA gel electrophoresis.
应用流式细胞仪分析和比较两组移植后1，2，3及4周小鼠脾脏内DC的数目、活化状态和随时间变化的DC动力学。
The numbers and activation status of splenic DC were observed by flow cytometry 1,2,3, and 4 weeks after the HSC transplantation.
方法运用倒置显微镜观察，流式细胞仪检测分析。
METHOD Cell apoptosis was observed with inverted microscope and flow cytometer.
结论PKH26染色结合荧光抗体标记和流式细胞术，是分析淋巴细胞及其亚群增殖动力的有力工具。
Conclusion PKH26 staining combined with fluorescent antibody labeling and flow cytometry were powerful tools for analysis of proliferation of lymphocytes and their subsets.
方法：采用间接免疫荧光流式细胞术，分析K562细胞表面TRAIL分子的表达。
METHODS: The expression of TRAIL on K562 cells was detected by indirect immunofluorescence staining and flow cytometry.
方法运用直接包被法制备免疫磁珠，并以流式细胞仪分析。
Methods Immunomagnetic beads were prepared by direct antibody coating and analysed by flow cytometry.
用流式细胞仪分析细胞周期与凋亡状况。
方法采用三色免疫荧光直接标记法及多参数流式细胞术分析13例多发性骨髓瘤的免疫表型。
Methods Three-colour direct immunofluorescence staining and multiparameter flow cytometry were used for analysis of 13 samples of immunophenotyping of multiple myeloma patients.
方法骨髓有核细胞免疫荧光标记后用流式细胞术分析。
Methods Bone marrow nuclear cells (BMNCs) were labeled by immunofluorescence and analyzed by flow cytometry.
结果形态学变化、流式细胞仪分析和TUNEL法结果均证实含鲜壁虎血清在体外可诱导C6胶质瘤细胞凋亡；
Results The C6 glioma cell apoptosis induction of GFP contained serum in vitro could be confirmed by morphological examination, flow cytometry analysis and TUNEL method.
采用MTT比色法、平板克隆形成实验、流式细胞术和MTS比色法分析SLP鄄2对TE12细胞的影响。
MTT assay, plate clone formation assay, flow cytometry, and MTS assay were performed to measure the effect of SLP-2 on TE12 cells.
流式细胞术分析发现，转化细胞细胞周期发生改变。
Changes in cell cycle of the transformed cells were observed with flow cytometry.
方法：采用间接免疫荧光标记，流式细胞术分析。
Methods Indirect immune fluorescent labeling and flow cytometry were employed.
方法应用流式细胞术分析人胃癌MGC803细胞在DADS处理前后细胞周期分布的变化。
Methods cell cycle of MGC803 cell treated with DADS in vitro was analyzed by flow cytometry.
方法利用免疫细胞化学，蛋白质印迹法，RT -PCR和流式细胞术等方法分析细胞周期和对与细胞周期相关的基因表达进行研究。
Methods the cell cycle and the expression of related genes were analyzed by the methods of immunocytochemistry, protein blotting, RT PCR and flow cytometry.
光学显微镜下观察lcl的形态特征，利用流式细胞术分析LCL细胞膜表面分子CD 19和CD 23的表达水平。
Morphological characteristic of the established immortalized BLCL was observed by microscope and the expression of CD19 and CD23 on cellular surface was determined by flow cytometry.
方法利用流式细胞仪测定并分析视神经脊髓炎和健康对照的末梢血中CD 4 +记忆T细胞的表面受体。
Methods Examined surface receptors of memory CD4 + t cells by flow cytometry in peripheral blood from patients with NMO.
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