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作 者:刘树虎[1] 热比亚木.巴克 布帕提玛穆.阿布都克热穆 多力坤.买买提玉素甫
机构地区:[1]新疆大学生命科学与技术学院,新疆乌鲁木齐830046
出 处:《实验技术与管理》2017年第5期64-67,共4页Experimental Technology and Management
基 金:国家自然科学基金项目"新疆隔离人群的遗传多样性研究及流行病学资源数据库建立"(31460285);新疆维吾尔自治区自然科学基金项目"新疆阿尔克孜族隔离人群减数分裂重组热点遗传定位研究"(2013211A016);中国科学院计算生物学重点实验室开放课题(2014KLCB02)
摘 要:使用改良盐析法、改良酚/氯仿法、改良碘化钾法和试剂盒法,分别对在-80℃保存1~4年的维吾尔族人群血样提取DNA,分光光度仪检测DNA浓度和纯度,0.8%琼脂糖电泳检测,提取的DNA质量采用单因素方差分析比较。结果表明,改良碘化钾法提取DNA质量最好,其次是试剂盒法、酚/氯仿提取法,盐析法提取质量最差;冻存1~4年的血样提取的DNA浓度之间差异极显著(F=618.011,P=0.000),冻存1~4年的血样提取的DNA纯度之间差异极显著(F=27.090,P=0.000)。该研究基于经济实惠、方便操作,提取DNA质量的高低可以确定改良碘化钾法提取DNA质量最好;血样本冻存(-80℃)超过3年对提取的DNA质量有显著的影响。Objective: It is to analyze the factors affecting the quality of DNA extracted from the genomic DNA of whole blood frozen samples in Uygur population by different samples and freezing time.Methods: The blood samples at-80 ℃ for 1-4 years are extracted by the modified salting-out method, the modified phenol/chloroform method, the KI method and reagent box method.The concentration and purity of DNA are detected by the spectrophotometer and 0.8% agarose gel electrophoresis, and the extracted DNA quality is compared by the single factor variance analysis.Results: The improved KI method is the best to extract DNA, followed by the reagent box method and phenol/chloroform method, and the extraction quality by the salting-out method is the worst.The concentration of DNA extracted from the frozen blood samples for 1-4 years is significantly different (F=618.011, P=0.000) and so is its purity(F=27.090, P=0.000).Conclusion: The research is based on economic benefit and easy operation.The quality of DNA can be determined by the improved KI method, and the blood samples frozen (-80 ℃) for more than 3 years have significant effect on the quality of extracted DNA.
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