目的评价BACTEC 9050自动血培养仪的临床应用情况。
Objective to evaluate the clinical application of BACTEC 9050 automated blood culture system.
该培养仪将被用于培养皮肤癌细胞并且超强的辐射将靶向癌症源。
The culture facility will be used to grow skin cancer cells and the THz radiation will target the source of the cancer.
旋转培养仪提供的模拟微重力环境，可以提高工程化软骨的质量。
The results of this study demonstrated that the simulated microgravity by RCCS can improve the quality of tissue-engineered cartilage formed in vitro.
伴随寻求最优化的体外培养环境，旋转培养仪将成为生产组织工程化软骨极具潜力的选择，该技术也为实现关节软骨损伤的修复提供有效途径。
With the optimization of the culture conditions, RCCS may be employed for the production of tissue-engineered cartilage and become a promising means for human cartilage reconstruction.
他们在一个不锈钢培养皿里培育细菌，然后用激光蒸发它们的信号分子，把这些分子导入到质谱分析仪中并记录他们的状态。
They grow their bacteria on a stainless steel plate, and use a laser to vaporise their signalling molecules, feeding these into a mass spectrometer to catalogue the molecules present.
培养的细胞用70%乙醇固定，流式细胞仪测DNA含量。
The cultured cells were fixed with 70% ethanol, DNA analysis by Flow Cytometry.
方法体外甲基纤维素半固体培养观察各处理组k 562细胞的克隆形成，流式细胞仪评价细胞的凋亡状况。
METHODS in vitro methylcellulose semisolid culture was used for the evaluation of clonal formation of K562 cell line. Flow cytometer was used for detecting apoptosis.
方法用膜片钳记录仪在体外培养的不同时期，记录大鼠海马神经元GABA-A受体离子通道全细胞通道电流、电导的变化。
Methods: The patch clamp was used to record the changes in average whole cell current and the conductance of GABA-A receptor on cultured hippocampal neurons in different developing stages.
方法采用流式细胞仪技术对不同培养时间和不同培养条件下脐血cd 34 +细胞中pcna的表达水平和细胞周期进行了测定。
Methods Using flow cytometry, PCNA and cell cycle in CB CD34 + cells were measured in different conditions and different culture time.
与人骨髓间充质干细胞培养上清共孵育。流式细胞仪检测表面抗原。
The monocytes were co-incubated with supernatant from human marrow(mesenchymal) stem cells culture, and flow cytometer was used to detect surface antigen.
体外培养大鼠肝癌CBRH- 7919细胞，采用MTT法及流式细胞仪比较观察了非缩醛磷脂和缩醛磷脂对细胞生长及凋亡的影响。
The rat hepatoma cell CBRH-7919 were cultured and the effects of plasmalogens on proliferation and apoptosis of CBRH-7919 cell line were observed by the methods of MTT test and flow cytometry.
用溶剂自然挥发法培养了五个单晶，并采用CCD 单晶衍射仪测定了它们的晶体结构。
Five crystal structures are determined by CCD diffractometer after the single crystals were grown by slow evaporation at room temperature.
应用日立835-50型氨基酸自动分析仪测定阿苯达唑作用体外培养猪囊虫的氨基酸含量。
The contents of free amino acid (FAA) in Cysticercus cellulosae affected by albendazole in vitro were determined by using 835-50 type of automatic amino acid analyzer.
收集培养细胞，以流式细胞仪进行鉴定。
Some days later, the cells were collected and identified with FACS.
方法体外培养人脂肪抽吸术中获取的脂肪干细胞，体外培养至第二代，流式细胞仪检测免疫分子HLA、HLA、B7-1、B7-2、CD40的表达。
Methods ADSC was isolated from fat tissue by liposuction and culture expanded. Cells at passage2 were observed for the expression of HLA, HLA, B7-1, B7-2, CD40 and CD40L by FACs analysis.
方法：体外分离培养大鼠骨髓间充质干细胞，传代后通过形态学和流式细胞仪检测细胞表面标志物cd14, CD 44, CD 9,CD 34, CD 45表达。
METHODS: The rat BMSCs were separated and cultured in vitro. Following passage, expression of CD14, CD44, CD9, CD34 and CD45 was detected by morphology and flow cytometry.
方法：增菌分离培养后，以血清学为初试验，全自动细菌生化分析仪为确定试验结果。
Methods: After isolating, culturing and serological test, the bacterium was identified by automatic biochemical analyzer.
方法：通过原代和传代培养，获得性状稳定的人牙周膜细胞，使用动态机械应变细胞加载仪对细胞进行1%、10%和20%动态牵张应变加载。
METHODS: Primary human periodontal ligament cells were obtained and passaged. Then the cells were stretched by dynamic mechanical strain unit with 1%, 10% and 20% strain at different time.
该室拥有超净工作台、人工气候箱、厌氧培养箱、全自动微生物鉴定系统、智能生物图像导航仪等研究设备。
The laboratory has research instruments, such as a clean bench, artificial climate chamber, anaerobic incubator, automated microbial identification systems and bio-image navigation instrument.
方法采用破骨细胞与骨片的体外共培养法和显微摄片、显微光密度仪扫描及计算机图像分析技术。
Methods Rabbit's osteoclastes were coincubated with bone slices and microphotographed, microdensitometric scanned and analyzed by computer image analysis system.
结果与结论：体外分离培养的脂肪源干细胞生长稳定，扩增速度快。流式细胞仪检测结果显示其高表达干细胞相关抗原。
RESULTS and CONCLUSION: ADSCs could be expanded steadily in vitro and flow cytometry revealed high expression of stem cell-associated markers.
使用倍性分析仪，对48种培养多年不同基因型的柑橘愈伤组织的细胞DNA含量进行了测定。
The cell DNA content of forty-eight Citrus calli of different genotype were measured by using the Ploidy Analyser.
使用倍性分析仪，对48种培养多年不同基因型的柑橘愈伤组织的细胞DNA含量进行了测定。
The cell DNA content of forty-eight Citrus calli of different genotype were measured by using the Ploidy Analyser.
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