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排序方式: 共有330条查询结果,搜索用时 15 毫秒
131.
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全血中DNA6种提取方法的比较 总被引:1,自引:0,他引:1
目的 比较经典有机法、改良有机法、常规Chelex-100法、IQ法、Qiagen法及SP法6种方法在提取DNA纯度和得率上的差异.方法 收集10名健康志愿者的静脉全血各5mL,分别采用6种方法提取基因组DNA,通过紫外分光光度仪和荧光定量分析技术检测产物的纯度和浓度,计算得率,并使用统计软件对结果进行分析.结果 常规Chelex-100法所得DNA的纯度明显低于其他方法,而另外5种方法所得DNA纯度的差异不具有统计学意义.改良有机法得率最低,IQ法得率最高.统计结果表明试剂盒方法抽提全血DNA的得率明显高于经典有机法、常规Chelex-100法和改良有机法,其差异具有统计学意义.结论 与有机法和常规Chelex-100法相比,高质量试剂盒类方法更有利于法医学检材的DNA抽提. 相似文献
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C. Gehrig D. Kummer V. Castella 《Forensic Science International: Genetics Supplement Series》2009,2(1):85-86
The aim of this study was to evaluate the forensic protocol recently developed by Qiagen for the QIAsymphony automated DNA extraction platform. Samples containing low amounts of DNA were specifically considered, since they represent the majority of samples processed in our laboratory. The analysis of simulated blood and saliva traces showed that the highest DNA yields were obtained with the maximal elution volume available for the forensic protocol, that is 200 μl. Resulting DNA extracts were too diluted for successful DNA profiling and required a concentration. This additional step is time consuming and potentially increases inversion and contamination risks. The 200 μl DNA extracts were concentrated to 25 μl, and the DNA recovery estimated with real-time PCR as well as with the percentage of SGM Plus alleles detected. Results using our manual protocol, based on the QIAamp DNA mini kit, and the automated protocol were comparable. Further tests will be conducted to determine more precisely DNA recovery, contamination risk and PCR inhibitors removal, once a definitive procedure, allowing the concentration of DNA extracts from low yield samples, will be available for the QIAsymphony. 相似文献
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James Stray Vivian T. Nguyen Jacquelyn Benfield Rixun Fang Maxim Brevnov Lynda Treat-Clemons Greg Porter Manohar R. Furtado Jaiprakash G. Shewale 《Forensic Science International: Genetics Supplement Series》2009,2(1):64-65
Forensic DNA analysis is a multi-step process involving extraction of DNA, quantification of human DNA in the extract, amplification using multiplex STR systems, separation of products, and data analysis. The backlog of forensic casework is increasing worldwide. Automation is one significant way to alleviate the bottleneck of sample processing in forensic labs. The HID EVOlution™ Combination System described here is a robust, reliable sample processing platform, easily adapted to forensic laboratory workflows. Using a variety of forensic sample types including: blood stained FTA paper, cotton fabric and denim, dried blood spiked with known PCR inhibitors, saliva on cotton swabs, and semen stains, we found that yields of human DNA and STR profiles obtained with AmpFlSTR® Idenitfiler® kits were complete, highly reproducible, and equivalent to results obtained using the manual PrepFiler™ reagent extraction method. Automated operation was clean, and no cross-contamination was detected between extraction blanks and interspersed high DNA content samples. 相似文献
135.
Peter Zimmermann Kai Vollack Barbara Haak Michelle Bretthauer Andrea Jelinski Marga Kugler Jessica Loidl Werner Pflug 《Forensic Science International: Genetics Supplement Series》2009,2(1):62-63
Within the initial step of the forensic DNA analysis process, the DNA extraction efficiency and especially the removal of potential PCR inhibitors is crucial for subsequent steps, e.g. quantification by real-time PCR and amplification of short tandem repeats (STRs). The protocol of the PrepFiler™ Forensic DNA Extraction Kit was optimized for the application on a Tecan liquid handling workstation Freedom EVO® 150. This modified application of the PrepFiler™ technology was compared with respect to DNA yield, sensitivity and the ability to remove potential PCR inhibitors to an established routine method working on the same liquid handling workstation based on ChargeSwitch® Technology (CST) from Invitrogen. 相似文献
136.
死亡大鼠组织中总RNA提取的质量控制及方法评价 总被引:1,自引:0,他引:1
目的探讨不同商品化试剂盒在提取组织总RNA过程中的优劣与适用范围,为实验室的质量控制提供依据。方法采用以膜提取技术为基础(SV total RNA isolation system)和以异硫氰酸胍/苯酚法为原理(TRIzol总RNA提取试剂盒)的两种试剂盒对死亡大鼠心、肝、脾、肺、肾、脑组织进行总RNA的提取与评价鉴定,并使用琼脂糖变性凝胶电泳和2100芯片生物分析仪对提取的总RNA进行完整性鉴定和质量控制评价。结果两种商品化试剂盒提取的总RNA纯度与得率均可满足实验要求。各组织脏器中总RNA得率依次为脾脏>肝脏>肾脏>大脑>肺脏>心脏。结论与TRIzol总RNA提取试剂盒相比,SV Total RNA Isolation System提取时对操作人员熟练度要求较低,2100芯片生物分析仪有望替代凝胶电泳技术用于总RNA提取时的质量控制。 相似文献
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快速溶剂萃取技术是近几年出现的一种新的适用于复杂检材前处理的、高效、快速、简便、理想的萃取方法。快速溶剂萃取法的原理、特点、仪器装置与操作步骤、影响因素在刑事技术领域的应用。 相似文献