琼脂糖凝胶电泳检测断裂DNA ；
琼脂糖凝胶双扩实验测定抗体效价。
The titer of the antibody was assayed by the experiment of agarose biphasic diffusion.
用琼脂糖凝胶电泳检测两类卵的颗粒细胞凋亡。
Granulosa cell apoptosis was detected by agarose gel electrophoresis.
用琼脂糖凝胶电泳和细胞形态学观察细胞凋亡；
The thymocytes apoptosis was observed by agarose gel electrophoresis and cell morphology.
用琼脂糖凝胶电泳法分析凋亡细胞的DNA梯带。
Then DNA ladder zone of apoptosis cells was analyzed with the method of agarose gel electrophoresis.
扩增产物用琼脂糖凝胶电泳、溴化乙锭染色检测。
The PCR products were analyzed by electrophoresis in agarose gels stained with ethidium bromide.
目的：运用琼脂糖凝胶区带电泳进行蛋白尿的分析。
方法：用琼脂糖凝胶电泳法观察DNA的梯状条带。
Method:The DNA gradent bands were detected by agarose gel electrophoresis.
用荧光染色法和琼脂糖凝胶电泳观察细胞凋亡情况。
Fluorescence staining and agarose gel electrophoresis were used to study apoptosis.
琼脂糖凝胶电泳检测探针分子量大小与设计值相符。
All probes were corresponding to the predicted sizes confirmed by gel electrophoresis.
所得纯化物以1%琼脂糖凝胶电泳鉴定超螺旋质粒的含量。
The level of purified superhelix plasmids were measured by 1% agarose gel electrophoresis.
细胞核DNA琼脂糖凝胶电泳显示凋亡细胞特有的梯状条带。
The characteristic DNA ladder was found by the agarose gel electrophoresis for the nucleus DNA of transfected cells.
琼脂糖凝胶电泳显示，创伤脑组织DNA出现特异凋亡电泳带。
Gel electrophoresis of DNA extracted from traumatic brain tissues revealed internucleosomal fragmentation.
结论改良琼脂糖凝胶电泳法测定血清ldh同工酶应用前景良好。
Conclusion It is good application prospects to determine the LDH isoenzyme by improvement agarose gel electrophoresis method.
酶切产物经3％琼脂糖凝胶电泳分离后，紫外灯下检测酶切结果。
Restricted DNA products were then separated by useng 3% agarose gel electrophoresis and visuslized by UV light.
方法流式细胞术检测细胞凋亡；琼脂糖凝胶电泳检测断裂DNA；
Methods Flow cytometry were used to evaluate HepG2 cells apoptosis. agarose gel electrophoresis was used to detected DNA fragmentation;
采用血清琼脂糖凝胶区带电泳技术分析未经处理和处理后的蛋白尿样本。
The serum agarose gel zone electrophoresis technique was adopted to analyze the non-treated and treated samples of proteinuria.
以快流速琼脂糖凝胶为基质，采用直接偶联法制备丁基琼脂糖疏水层析介质。
Butyl-agarose chromatography media were prepared by direct coupling of butyl glycidyl ether (BGE) on agarose 4ff beads.
探索环氧氯丙烷法活化琼脂糖凝胶的最佳反应条件，建立活化反应动力学模型。
To explore the optimal condition of sepharose activation by means of epichlorohydrin and establish the kinetic model of activation process.
目的制定本实验室琼脂糖凝胶电泳法(age)测定血清蛋白的正常参考值范围。
Objective to establish the normal reference values of serum protein with agarose gel electrophoresis (AGE) in local clinical laboratory.
运用荧光光谱法、琼脂糖凝胶电泳法分别研究了配合物与DNA和BSA的作用。
The interaction with DNA and bovine serum albumin (BSA) were studied by fluorescence spectra and agarose gel electrophoresis.
方法：应用琼脂糖凝胶电泳试验、电镜照片制备及观察、粘附试验及质粒消除试验。
Methods Agarose gel electrophoresis of plasmid DNA, adherence test, and extract of plasmid were used. Electron microscope photos were prepared and observed.
HE染色、原位末端标记及琼脂糖凝胶电泳等实验证明，细胞的死亡方式为调亡。
The tests such as HE dye, still end labeling and gelose gel electrophoresis etc. have proved that the manner of cell death is apoptosis.
应用流式细胞术、DNA琼脂糖凝胶电泳、透射电镜等多种手段检测心肌细胞凋亡的改变。
The myocardial cells of each groups were taken for detecting apoptosis by the flow cytometry and DNA gel electro-phoresis.
经琼脂糖凝胶电泳分析载体与DNA结合力，并通过紫外分光光度计检测其载药量和包埋率；
The potential of adsorbing DNA on nanoparticles was analyzed by agarose gel electrophoresis and spectrophotometer.
方法优化RAPD及ISSR的PCR反应体系，对产物琼脂糖凝胶电泳结果进行数据统计。
Methods PCR reaction systems of RAPD and ISSR were optimized, and the agarose gel electrophoresis results were analyzed into statistic data.
有关等位基因的相关信息从PAGE胶上获得，聚类图构建的数据则来源于琼脂糖凝胶电泳。
The dendrogram was constructed from the agarose gel data, while the information of alleles was from PAGE gel.
用谷胱甘肽琼脂糖凝胶4b亲和介质从菌体裂解液中纯化了GST -MBD4融合蛋白。
The GST-MBD4 fusion protein was purified from cell lysates using glutathione Sepharose 4b affinity chromatography.
需要使用包括聚合酶链反应（PCR），琼脂糖凝胶电泳，探针的标记与检测等生物工程技术。
This technique employs standard operations of biomedical engineering, such as polymerase chain reaction(PCR), agarose gel electrophoresis, labeling and detecting of probe.
主要观测指标：紫外分光光度计检测吸光率（A值）及纯度、琼脂糖凝胶电泳、目的基因测序。
MAIN OUTCOME MEASURES:Ultraviolet spectrophotometer absorbance (A) and purity, agaroses gel electrophoresis, and objective gene sequencing.
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