Methods: HBV genotype was tested in 163 patients by real-time PCR.
方法 采用荧光PCR法对163例乙肝患者血清进行基因分型。
To explore the method of preparation for Hantavirus s segment standard plasmids of real-time PCR.
构建汉坦病毒S片段标准品，用于实时荧光定量pcr检测汉坦病毒。
Two real-time PCR assays for specific detection of Mycobacterium tuberculosis and Mycobacterium bovis were developed.
目的对结核分枝杆菌和牛分枝杆菌分别建立荧光PCR快速检测方法。
Myocardial ACE2 mRNA expression was respectively determined by real-time PCR (RT-PCR) in control group and diabetes group.
采用实时定量pcr (RT - PCR)检测正常及糖尿病大鼠心肌组织ace2的基因表达。
Methods Choose correct and effective PCR cycle number according to standard plasmid's amplification curve in real-time PCR;
方法根据标准质粒荧光定量PCR的扩增曲线选择合适有效的扩增循环次数；
Objective The serum HBV-DNA has been extensively detected by fluorescence-quantitative real time PCR (FQ-PCR) in our country.
目的目前国内较多的医院采用荧光定量的方法对血清中的HBV - DNA进行定量检测。
Multiplex PCR and real-time PCR are developed for simultaneous and quantitative detection of bacteria-producing biogenic amine.
利用多重PCR和实时定量PCR技术可以实现对葡萄酒中生物胺产生菌的快速定量检测。
The products of ruminant feed and cattle or sheep-derived feed from the enterprises and farms of 7 districts in Shaanxi province were detected by real-time PCR.
实时PCR对陕西省7个地市生产、经营和使用的反刍动物饲料产品和动物源性饲料产品（原料）进行了牛羊源成分检测调查。
Objective To set up a duplex quantitative real-time PCR (QPCR) assay with high sensitivity, specificity and rapidity to detect Candida krusei and Candida glabrata.
目的建立一种快速、灵敏、特异的鉴定克柔念珠菌和光滑念珠菌的双重实时荧光定量PCR方法。
The facility provides technical services for the clients, which include Oligonucleotide Synthesis, Protein Sequencing, DNA Sequencing, Real Time PCR/Allele Detection.
该机构为客户提供寡核苷酸合成、蛋白质测序、DNA测序、实时PCR和等位 基因检测等技术服务。
Methods Serum samples from 188 chronic hepatitis B patients with lamivudine therapy were collected and quantitatively tested with real-time PCR for HBV DNA and YMDD mutations.
方法将接受拉米夫定治疗的188例患者根据治疗时间进行分组，采用实时荧光PCR方法定量检测各组患者血清HBVDNA水平和酪氨酸-甲硫氨酸-天冬氨酸-天冬氨酸（YMDD）变异。
The aim of this assay is to investigate on the TaqMan Real-time PCR method for phytoplasma general detection which has the superiorities in saving time and preventing contamination.
本实验意在研究一种能够应用于植原体初筛，并且不易污染，易操作耗时短的通用方法。
This real-time PCR reaction system is highly specific, reliable, high sensitivity for detecting pathogenic fungus which could be useful for the diagnosis of clinical fungus infection.
建立的实时荧光PCR方法能特异、灵敏的检测临床病原真菌，为临床真菌感染的诊断提供了一种快速、准确的方法。
The results of real-time PCR analysis revealed that TAFFC transcripts were steady in incompatible interaction of wheat and stripe rust, whereas down-regulated in compatible interaction.
实时荧光定量PCR结果表明，该基因在受到条锈菌诱导下，在亲和组合中表达趋势明显下调，而在非亲合组合中的表达趋势比较稳定。
Methods We quantified Caspase-8 expression levels in 96 esophageal cancer issues and their matched normal esophagus tissues by using real-time PCR assay and immunohistochemistry staining.
方法采用实时荧光定量聚合酶链反应和免疫组化染色法检测96例食管癌患者的食管癌组织和癌旁正常组织Caspase-8表达。
The autopsy samples, including heart, liver, spleen, lung, kidney and brain, were ground and detected by Real-time PCR. According to the standard curve, virus load of H5N1 AIV was calculated.
将人禽流感死亡病例的尸解标本，包括心、肝、脾、肺、肾、脑等组织标本研磨处理后，进行荧光定量pcr检测，并根据标准曲线推算H5N1禽流感病毒的病毒载量。
Finally, the expression levels of the candidate genes were further confirmed by quantitative real-time PCR using a new set of samples (20 narcolepsy-cataplexy patients and 20 healthy controls).
最后，用定量实时PCR法在一组新样本(20名发作性睡病-猝倒患者和20名健康对照)中进一步确认候选基因的表达水平。
Finally, the expression levels of the candidate genes were further confirmed by quantitative real-time PCR using a new set of samples (20 narcolepsy-cataplexy patients and 20 healthy controls).
最后，用定量实时PCR法在一组新样本(20名发作性睡病-猝倒患者和20名健康对照)中进一步确认候选基因的表达水平。
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