期刊文献+
共找到10篇文章
< 1 >
每页显示 20 50 100
QIAGEN实时PCR与COBASTaqMan检测血清HBVDNA预测慢性乙型肝炎肝组织病理状态的性能比较 被引量:6
1
作者 张占卿 陆伟 +5 位作者 王平安 王雁冰 周新兰 丁荣蓉 李秀芬 黄丹 《肝脏》 2016年第4期241-247,252,共8页
目的比较QIAGEN实时PCR与COBAS TaqMan检测血清HBV DNA水平预测慢性乙型肝炎肝组织病理状态的性能。方法慢性乙型肝炎患者278例,其中HBeAg阳性和阴性分别为162例和1 16例。采用QIAGEN实时定量PCR和COBAS TaqMan系统检测血清HBV DNA。肝... 目的比较QIAGEN实时PCR与COBAS TaqMan检测血清HBV DNA水平预测慢性乙型肝炎肝组织病理状态的性能。方法慢性乙型肝炎患者278例,其中HBeAg阳性和阴性分别为162例和1 16例。采用QIAGEN实时定量PCR和COBAS TaqMan系统检测血清HBV DNA。肝组织病理学诊断采用Scheuer评分系统,其中病理学分级和分期包括G0~G4和S0~S4。结果血清HBV DNA(QIAGEN)和HBV DNA(C()BAS)在HBeAg阳性患者G2与G3,S1、S2、S3与S4之间的差异有统计学意义(P均〈0.05);在HBeAg阴性患者G1与G2、G3,S1与S2、S3、S4之间的差异有统计学意义(P均〈0.05)。血清HBV DNA(QIAGEN)与HBV DNA(COBAS)定量的不一致率,在HBeAg阳性患者G1-2、G3和S1-3、S4分别为4.24%(5/1 18)、9.09%(4/44)和3.68%(5/136)、7.69%(2/26),在HBeAg阴性患者G1、G2-3和S1、S2-4分别为6.02%(5/83)、3.03%(1/33)和3.29%(2/61)、3.64%(2/55)。血清HBV DNA(QIAGEN)和HBV DNA(COBAS)预测HBeAg阳性患者≥G3、≥S4的ROC曲线下面积分别为0.645和0.695、0.703和0.755,预测HBeAg阴性患者≥G2、≥S2的ROC曲线下面积分别为0.848和0.817、0.756和0.756。血清HBV DNA(QIAGEN)和HBV DNA(COBAS)预测HBeAg阳性患者≥S4的最佳截断值分别为≤3.784×10~6 IU/mL和≤6.668×10~7IU/mL,对应的灵敏度、特异度分别为0.654和1.000、0.735和0.581;预测HBeAg阴性患者≥G2的最佳截断值分别为≥5.821×10~3IU/mL和≥9.311×10~3 IU/mL,对应的灵敏度、特异度分别为0.970和0.909、0.614和0.651。结论血清HBV DNA预测肝组织病理状态的特点为预测HBeAg阴性患者≥G2的效能最大,并且血清HBV DNA(QIAGEN)与HBV DNA(COBAS)预测HBeAg阴性患者≥G2的性能有高度一致性。 展开更多
关键词 HBV DNA定量 qiagen试剂 COBAS TaqMan系统 慢性乙型肝炎 肝组织 病理学
暂未订购
QIAGEN质粒DNA纯化柱的再生利用
2
作者 刘忠湘 缪军 +3 位作者 王宪锋 李王旬 雷俊川 薛采芳 《第四军医大学学报》 2000年第7期S203-S204,共2页
关键词 DNA提取 纯化柱 再生利用 qiagen 质粒
在线阅读 下载PDF
15种常见食(药)用菌的3种总DNA提取方法比较研究 被引量:14
3
作者 江树勋 邵碧英 +4 位作者 陈文炳 李寿崧 王泽生 朱晓南 廖剑华 《食品科学》 EI CAS CSCD 北大核心 2004年第5期36-40,共5页
本文研究了15种主要食(药)用菌共16个样品的3种总DNA提取方法之比较,它们分别是CTAB法、食品DNA提取试剂盒法和QIAGEN试剂盒法。提取结果分别经过核酸蛋白分析仪、电泳以及RAPD检测。紫外检测结果表明3种方法提取到的总DNA质量均不理想... 本文研究了15种主要食(药)用菌共16个样品的3种总DNA提取方法之比较,它们分别是CTAB法、食品DNA提取试剂盒法和QIAGEN试剂盒法。提取结果分别经过核酸蛋白分析仪、电泳以及RAPD检测。紫外检测结果表明3种方法提取到的总DNA质量均不理想,电泳结果表明3种方法均能提取出小平菇、红菇、香菇、双孢蘑菇、竹荪、黑木耳、姬松茸等7种食(药)用菌总DNA,RAPD检测结果表明CTAB法适用于所有15种食(药)用菌提取用于PCR的总DNA。根据以上结果,我们认为可以选用CTAB法作为在检测这些食(药)用菌的转基因成分时的总DNA提取方法。 展开更多
关键词 食用菌 药用菌 总DNA 提取方法 比较研究 CTAB法 食品DNA提取试剂盒法 qiagen试剂盒法
在线阅读 下载PDF
两种方法提取DNA在α地中海贫血基因检测中敏感性的比较
4
作者 陈辉 周迎春 马福广 《中国优生与遗传杂志》 2002年第5期12-12,22,共2页
目的 寻找α地中海贫血基因检测中提取DNA的快速、敏感、准确的方法。方法 全血DNA提取采用Qiagen快速法及表面活性剂快速法 ,并用双重PCR法进行α -地中海贫血基因的检测。结果  6 0例经典法提取DNA并用双重PCR测定确定为α -地中... 目的 寻找α地中海贫血基因检测中提取DNA的快速、敏感、准确的方法。方法 全血DNA提取采用Qiagen快速法及表面活性剂快速法 ,并用双重PCR法进行α -地中海贫血基因的检测。结果  6 0例经典法提取DNA并用双重PCR测定确定为α -地中海贫血患者 ,经Qiagen法提取DNA进行双重PCR检测 ,阳性为 6 0例 ,检出敏感性为 10 0 % (6 0 / 6 0 ) ,而表面活性剂快速法检出阳性为 10例 ,敏感性约为 16 7% (10 / 6 0 ) ,经非参数检验中的麦克内尔马检验 ,两者有统计学意义。结论 :表面活性剂快速法提取DNA进行α -地中海贫血基因检测漏诊率高 ,不能用于标本提取DNA进行α-地中海贫血基因检测 ;Qiagen法尽管成本较高 ,但是它检出敏感性高 ,准确、快速 ,尤其在诊断如α 展开更多
关键词 提取 DNA Α地中海贫血 基因检测 敏感性 qiagen 经典法
暂未订购
AmpFISTR Sinofiler快速PCR扩增初探 被引量:3
5
作者 王鸿迪 董海成 +1 位作者 于俊峰 邵武 《中国法医学杂志》 CSCD 2012年第5期397-398,共2页
本文实验选择AmpFISTRSinofiler试剂盒作为研究对象,对如何缩短PCR扩增时间进行了初步探讨。1材料与方法1.
关键词 法医物证学 AmpFISTR Sinofile试剂盒 qiagen FAST CYCLING PCR试剂盒 快速PCR扩增
原文传递
不同核酸提取试剂盒对血浆游离DNA提取效果的比较 被引量:2
6
作者 方仲表 沈伟锋 +3 位作者 饶焕新 章余旋 潘志文 吴欧 《国际检验医学杂志》 CAS 2022年第8期979-983,989,共6页
目的比较北京天根生化科技有限公司生产的大体积游离核酸提取试剂盒(磁珠法,货号:DP-710,以下简称天根)与德国Qiagen公司生产的Circulating Nucleic Acid kit(硅胶膜吸附柱法,货号:55114,以下简称Qiagen)对血浆当中游离DNA(cfDNA)的提... 目的比较北京天根生化科技有限公司生产的大体积游离核酸提取试剂盒(磁珠法,货号:DP-710,以下简称天根)与德国Qiagen公司生产的Circulating Nucleic Acid kit(硅胶膜吸附柱法,货号:55114,以下简称Qiagen)对血浆当中游离DNA(cfDNA)的提取效果。方法收集Qiagen和天根试剂盒的基本情况,采用浙江省肿瘤医院提供的临床血浆样本,用Qiagen和天根分别提取血浆样本中的cfDNA。用超微紫外分光光度仪分析两种试剂盒提取得到cfDNA的浓度和纯度。采用人表皮生长因子受体(EGFR)突变基因检测试剂盒(多重荧光PCR法)评价两种试剂盒提取血浆中cfDNA的提取效果,通过扩增结果的Ct值分析两种不同试剂盒对人EGFR基因突变的检出率和重复性的影响。结果在cfDNA提取浓度、纯度方面,Qiagen的cfDNA提取浓度明显高于天根,且Qiagen提取得到的cfDNA纯度更优;在人EGFR突变基因阳性检出率方面,Qiagen阳性检出率为100%,天根阳性检出率为85%;在重复性方面,Qiagen试剂盒提取的cfDNA的检出结果Ct值的变异系数(CV)均小于5%,而天根试剂盒有分部分CV超过5%。结论Qiagen试剂盒在cfDNA提取浓度、纯度,人EGFR突变基因的阳性检出率、重复性方面的表现均要优于天根试剂盒。 展开更多
关键词 天根 qiagen 核酸提取 游离DNA EGFR突变基因
暂未订购
核桃叶片总RNA提取方法的比较研究 被引量:2
7
作者 陈新 刘洪对 +3 位作者 贾建云 徐丽 张力思 刘庆忠 《山东农业科学》 2014年第2期11-12,16,共3页
通过对比Trizol、EASYspin和Qiagen 3种试剂盒提取方法,探讨适合核桃叶片总RNA提取的有效方法。结果表明EASYspin试剂盒提取的RNA纯度较高、完整性好,试验用时较短,且试剂盒成本较低。
关键词 核桃 JUGLANS regia L EASYspin RN09
在线阅读 下载PDF
Low and High Risk Human Papillomavirus in the Oral Mucosa of Mexican Women with Genital Papillomavirus
8
作者 Ana María Fernández Dora Rosete +3 位作者 Sergio Pedraza Fidencio Mejía José Delgado María Eugenia Manjarrez 《Open Journal of Medical Microbiology》 2013年第1期62-69,共8页
Background: Human papillomaviruses (HPV) are implicated in cervical cancer and, recently in oral cancer. In Mexico, there are few studies on oral cancer, therefore the interest in identifying the HPV frequency of low ... Background: Human papillomaviruses (HPV) are implicated in cervical cancer and, recently in oral cancer. In Mexico, there are few studies on oral cancer, therefore the interest in identifying the HPV frequency of low and high risk in samples of the oral and cervical cavities, and determining some risk factors. Objective: To determine the frequency of high and low risk HPV infection in the oral cavity of women with cervical HPV, and to correlate the infection site with risk factors. Materials and Methods: Eighteen female patients between 24 and 53 years, with antecedents of genital HPV infection were included. Both samples of oral cavity and cervix were obtained. DNA extraction from the epithelial cells was performed using the Qiagen kit. PCR was done and the amplicon was observed in 2% agarose gels stained with ethidium bromide. A correlation of HPV infection and risk factors was done. Results: HPV-DNA was detected in the 67% of both samples. The frequency of oral and cervix low risk HPV-DNA was 50%, while high risk HPV-DNA in oral cavity was detected in 17%, and 39% in the cervix. The study of the risk factors involved in HPV infection showed that the participants had the habits of smoking 39%;alcohol drinking 28%;and 78% oral sex. Conclusion: The results showed a high frequency of HPV (67%) infection in the oral and genital mucosas, suggesting that patient’s habits could contribute to the infection;the presence of HPV in the oral mucosa may act as reservoir for new HPV infections. 展开更多
关键词 Human PAPILLOMAVIRUSES (HPV) HPV-DNA qiagen KIT
暂未订购
Anthropological analyses of 30 insertion/deletion autosomal markers in five major ethnic groups of Pakistan
9
作者 Muhammad Adnan Shan Julie Mechlenborg +2 位作者 Rebecca Roen Claus Bosting Niels Morling 《Forensic Sciences Research》 CSCD 2022年第2期202-206,共5页
We investigated the forensic efficacy of the 30 insertion/deletion(Indel)markers included in the Qiagen Investigator■DIPplex kit in 529 Pakistani individuals from five major subpopulations in Pakistan(Punjabi,Pashtun... We investigated the forensic efficacy of the 30 insertion/deletion(Indel)markers included in the Qiagen Investigator■DIPplex kit in 529 Pakistani individuals from five major subpopulations in Pakistan(Punjabi,Pashtun,Sindhi,Saraiki,and Baloch).In the Sindhi population,the distribution of HLD81 and HLD97 alleles deviated from Hardy-Weinberg equilibrium after Bonferroni correction.The combined match probability ranged from 2.0E-12(Pashtun and Baloch)to 1.0E-12(Sindhi),and the mean paternity exclusion power varied from 0.995(Punjabi,Sindhi,and Saraiki)to 0.996(Pashtun and Baloch).The high combined power of discrimination(0.99999999999997)and low combined match probability(1.7E-12)for all subpopulations studied support the utility of the 30 Indel markers for forensic identification in the studied subpopulations.The allele frequencies of the Indel markers in the Pakistani subpopulations were compared with those from 18 other populations.The results show that the populations clustered according to geography.The subpopulations investigated in this work showed a close genetic relationship with others from Pakistan,as well as with South Central Asian and Middle Eastern populations.The results suggest that the Investigator■DIPplex kit can be useful as a supplementary tool for human identification in the five Pakistani subpopulations investigated in this study. 展开更多
关键词 Forensic sciences forensic genetics qiagen investigator■DIPplex kit ANTHROPOLOGY population genetics individual identification
原文传递
The Evaluation of Insertion and Deletion Polymorphism in Population and Personal Identification Amidst Chinese Populations
10
作者 Hui Sun Caiyong Yin +5 位作者 Lei Shang Chong Wang Kaiyuan Su Wanshui Li Feng Chen Shilin Li 《Journal of Forensic Science and Medicine》 2018年第3期115-121,I0001-I0003,共10页
For comprehensive understanding of practical application and evaluation on the power of30 commonly used InDeis(Qiagen Investigator DIPplex®kit),we captured population data from 25 Chinese populations and employed... For comprehensive understanding of practical application and evaluation on the power of30 commonly used InDeis(Qiagen Investigator DIPplex®kit),we captured population data from 25 Chinese populations and employed F-statistics for population genetics analysis.The results indicated that the distributions of allelic frequencies among populations were in different levels.Furthermore,the phylogeny confoiming pairwise FST distances showed that the difierentiation of majority populations were consistent with their geographic locations and historic dispersals.We conduct the comprehensive correlation analysis between FST and heterozygosity of30 InDel loci and provided strong evidence for ongoing InDei loci selection.The Fst values of 30 InDels were calculated within 25 Chinese populations,and then,these loci were characterized definitely based on their roles in population genetics or individual identification.Data indicated that 17 InDels with FST<0.01 could be utilized regarding Chinese individual identification(total discrimination power=0.999985 and cumulative matching probability=0.00000009).We comprehensively reconstructed the population structure and filled the gap of evaluating the ability of InDels in personal as well as population identification.The application of InDel loci in the forensic area would convincingly promote the development matter of forensic population identification and personal discrimination. 展开更多
关键词 Chinese populations insertion and deletion personal Identification population identification qiagen investigator dipplex®kit
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部