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以空质粒转染组为对照。Null vector transfection as the control.
基因脉冲导入技术应用前景十分广泛。The application prospect of Gene pulser transfection is very extensive.
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培养液中的白蛋白、血清可降低转染效率。Albumin, serum in the culture medium decreased the transfection efficiency.
培养液中的白蛋白、血清可降低转染效率。Albumin and serum in the culture medium decreased the transfection efficiency.
利用这种方法我们试图发展一种新的对悬浮式细胞进行基因转染的方法。We explore this technique as a novel gene transfection method for floating cells.
发展了两种基于二氧化硅微颗粒的基因转染新方法。Two new gene transfection methods have been developed based on silica micro-particles.
大鼠骨髓间质干细胞可以成为PEX基因稳定转染的载体细胞吗?。Can bone marrow mesenchymal stem cells be used as PEX gene stable transfection vectors?
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TUNEL染色显示，E10细胞出现典型的凋亡特征。TUNEL staining showed typical apoptosis characteristics of E10 cells after transfection.
应用基因转染技术可能是解决这些问题的途径之一。The gene transfection technology might be one of the approaches to resolve these issues.
本文仅就目前体内心肌基因转染技术的进展作一综述。This article reviews about progress in gene transfection technique to myocardium in vivo.
探讨IL-18基因转染对大鼠C6胶质瘤细胞生长特性的影响。To explore the effects of IL-18 gene transfection on the proliferation of C6 glioma cell.
并将外源基因ALB亚克隆入该调控序列内，转染C127细胞，经免疫组化法检测其表达情况。Subclone the exogenous gene ALB into the regulating sequence for transfection of C127 cells.
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基因克隆和基因转染技术的发展让内耳基因治疗前景广阔。Developments of gene cloning and gene transfection have broaded outlook of NT-3 gene therapy.
用小鼠实体瘤模型研究基因转染对肿瘤生长的抑制。The inhibitory effect of IL-24 gene transfection in mice solid tumor was observed and measured.
本研究旨在构建人血管内皮生长因子D重组腺病毒，为基因转染研究作准备。VEGF-D recombinant adenovirus was constructed and confirmed before the studies of gene transfection.
同时通过抗生素的方法对转染后的幼苗进行初步筛选，这部分内容正在进行中。Meanwhile, to filter the seedings with transfection by using the method of antibiotics is on study now.
与未转染者相比，转染肝细胞的缺氧-复氧损伤程度较轻。The hypoxia-reoxygenation injury to liver cells with transfection was milder than that to control cells.
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转染是指不用病毒而直接将DNA或者RNA导入体细胞。Transfection is the process of introducing DNA or RNA into a cell without using viruses to deliver them.
转染了鼠CD40配体基因的H22细胞在同源小鼠中的致瘤性降低。The tumorigenicity of H22 cells was abolished by in vitro transfection with mCD40L gene in syngeneic mice.
流式细胞仪检测转染效率，MTT法检测细胞毒性。The efficiency of transfection is examined by Flow CytoMeter and the cytotoxicity is evaluated with MTTassay.