1.Compare the results of ABI Prism 377 sequencer and ABI Prism 3100 sequencer.
b．比较ABI Prism 377型测序仪和ABI Prism 3100型测序仪进行定量分析时的差异。
2.4. The sensitivity of ABI Prism 3100 sequencer is higher than ABI Prism 377sequencer.
4．分析荧光KR产物时，ABI Prism 3100型叙序仪比ABI Pns。 377型测序仪有更高的敏感性
3.In this paper we firstly introduce the history of Semantic Web, its architecture and some key technologies like XML, RDF(S) and ontology. Some metadata such as DC, PRISM and XMP also be introduced, extremely the XMP packet technology.
本文首先介绍了语义Web的历史、体系结构和几个关键技术——XML、RDF（S）和Ontology，及DC、PRISM、XMP元数据标准，并着重介绍了Adobe公司的XMP包技术。
4.The DNA amplified from ompl-nPCR was sequenced by ABI PRISM 377 DNA sequencer.
用ABI PRISM 377型全自动DNA 测序仪测序；
5.Real-time relative quantitative reverse transcription -polymerase chain reaction was performed using ABI PRISM 7500 Sequence Detection System and SYBR Green I chemistry.
采用ABI PRISM 7500 Sequence Detection System和SYBR GreenⅠ进行实时定量RT-PCR。 以β_2-MG为内参照，按1／2(~(Ct)FOXP3~(-Ct)β2-MG)公式计算FOXP3 mRNA相对表达量。
6.The ABI Prism 7500 Sequence Detection System using Taqman fluorogenic probes was used to quantify target gene. PML/RARα mRNA was detected by Q-PCR in 46 APL patients and 40 non-APL patients. The normalized quotient (NQ) of PML/RARα mRNA was calculated as followings: NQ= PML/RARα mRNA copy numbers/ABL mRNA copy numbers.
利用ABI Prism7500型Q-PCR仪对46例初诊APL患者和40例非APL患者骨髓标本进行检测,PML/RARαmRNA定量结果以校正比值(NQ)表示,NQ=PML/RARαmRNA拷贝数/ABLmRNA拷贝数;
7.Interferon-y (IFN-y) and interleukin-4 (IL-4) mRNA expression in PBMC was quantified with TaqMan Real-time PCR using an ABI PRISM 7700 Sequence Detector System (Perkin-Elmer Applied Biosystems).
mRNA的定量测定是在ABI PRISM 7700序列检测系统上应用TaqMan Real-time PCR技术进行的。
8.Discrete Time Markov Chains(DTMCs) of the model was presented by using probabilistic model checking technique. Compared with two familiar time out schemes belonging to predictive schemes by PRISM,the energy efficiency of this scheme is better as a whole.
然后应用概率模型检测技术将其建模为DTMCs,并使用PRISM对这一策略和DPM中另外两种常用预测策略进行了比较,结果表明这一优化策略对网络的拥塞、延时及可靠性影响较小,其总体节能效果优于上述两种预测策略。
9.Rapid and Economic DNA Sequencing Using ABI PRISM~(TM) 310 Sequencer
应用ABI PRISM~(TM)310测序仪进行快速且经济的DNA测序
10.A set of primers were designed to carry out a multiplex PCR for three STR loci D20S601, D6S474 and D6S2418. Using our primer set, three STR loci were amplified and the products of the multiplex PCR were genotyped by ABI PRISM(?) 310 Genetic Analyzer. The multiplex STR system was evaluated under variety conditions.
方法 对5个新的STR基因座进行群体遗传学研究,并对D20S601、D6S474、D6S2418基因座原始引物进行了改进,利用传统复合扩增技术扩增,ABI PRISM~(?)
