检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
机构地区:[1]中国动物疫病预防控制中心,北京102618 [2]青岛农业大学化学与药学学院,山东青岛266109
出 处:《黑龙江畜牧兽医》2016年第2期247-250,共4页Heilongjiang Animal Science And veterinary Medicine
基 金:农业部公益性行业项目/农业部(201303038-8)
摘 要:为了快速、灵敏检测反刍动物饲料中的牛羊源成分,试验采用双重荧光PCR方法,根据线粒体环氧酶2(Cox2)和细胞色素b(Cytb)基因,分别设计牛羊特异性引物序列,基于SYBR荧光PCR技术,分析熔解曲线,根据吸收峰的位置不同,定性识别牛羊源成分。结果表明:试验测得单重牛PCR产物熔解曲线吸收峰对应的熔解温度为(76.0±0.5)℃,羊PCR产物熔解曲线吸收峰对应的熔解温度为(81.5±0.5)℃,且双重体系吸收峰与单重对应的熔解温度吻合,说明试验可行。试验检测牛成分的灵敏度为0.01%,检测羊成分的灵敏度为0.1%。该方法可以同时定性检测饲料中牛羊源性成分,成本较低,节省时间,可以应用于高通量的实际检测样品,灵敏度较高。To rapidly and sensitively detect cattle - and sheep - derived ingredients in ruminant feedstuff, a method of duplex real - time PCR was used to design the sequences of specific primers for cattle and sheep according to mitochondrial cyclooxygenase 2 (Cox2) and cytochrome b (Cytb), respectively. The melting curves were analyzed based on SYBR fluorescence PCR technology, and then cattle- and sheep- derived ingredients were qualitatively identified according to different positions of the absorption peak. The results showed that the melting temperatures corresponding to the absorption peaks of melting curves of cattle and sheep singlet PCR products were (76.0 ± 0.5 ) and (81.5± 0.5 )℃, respectively, while the absorption peak of duplex system was consistent with the melting temperatures corresponding to single system, indicating that the test was feasible. The detection sensitivity of the method for cattle - and sheep - derived ingredients was 0.01% and 0.1%, respectively. The results indicate that the method of duplex fluorescence PCR can simultaneously and qualitatively detect cattle - and sheep - derived ingredients in feedstuff, which has lower costs and can save time. The method can be applied to detect actual samples with high throughput, which has higher sensitivity.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.7