对99只人工养殖的果子狸采用聚合酶链反应进行检测。
PCR method weas used to detect 99 domesticated Paguma larvata.
聚合酶链反应(PCR)测定。
聚合酶链反应。
方法聚合酶链反应。
聚合酶链反应-微孔板杂交法检测输血传播病毒。
DNA detection of tt virus DNA by polymerase chain reaction -microplate hybridization.
方法采用单管四重聚合酶链反应(PCR)技术。
Methods Single barrel four-seat PCR technique was performed.
目的：探讨聚合酶链反应在沙眼诊断中的临床应用价值。
Objective: To investigate the clinical value of Polymerase Chain Reaction in the diagnosis of trachoma.
近年来聚合酶链反应(PCR)已应用于口腔细菌的研究。
Polymerase chain reaction (PCR) extensively utilized for research about oral bacteria recently.
其技术主要包括胚胎活检、聚合酶链反应及荧光原位杂交。
The basic techniques currently used involve embryo biopsy, the polymerase chain reaction and fluorescence in situ hybridization.
半定量反转录-聚合酶链反应验证了芯片分析结果的可靠性。
The results of semi-quantitative RT-PCR experiments supported the reliability of our microarray analysis.
目的探讨克隆聚合酶链反应(PCR)扩增产物的简便方法。
Objective To explore simple method for cloning the products amplified with polymerase chain reaction (PCR).
目的建立应用任意引物聚合酶链反应进行真菌菌型鉴定的方法。
Objective To establish the method to identify fungus using the arbitrarily primed polymerase chain reaction (APPCR).
目的评价聚合酶链反应探针杂交酶显色方法，检测结核分支杆菌。
Objective To evaluate the value of PCR-probe hybridization-ELISA for detection of mycobacterium tuberculosis(M. tuberculosis).
目的评价胸膜活检组织行聚合酶链反应对结核性胸膜炎的诊断价值。
Objective To evaluate the value of PCR to pleural biopsy specimen in the diagnosis of tuberculous pleuritis.
现行的多元聚合酶链反应(PCR)技术最多只能在50种生物内进行一次检测。
Current multiplex polymerase chain reaction (PCR) techniques can at most offer detection from among 50 organisms in one test.
方法：聚合酶链反应（PCR）、单链构象多态性（SSCP）分析。
Methods:Polymerase chain reaction (PCR) and single strand conformation polymorphism(SSCP) was used.
聚合酶链反应（PCR）确实就是一个给遗传物质加热和冷却的工艺而已。
Polymerase chain reaction is really just a process of heating and cooling genetic material.
目的探讨荧光定量聚合酶链反应（FQ-PCR）技术诊断结核病临床应用价值。
Objective To evaluate the clinical value of fluorescence quantitative PCR(FQ-PCR) technique in diagnosing tuberculosis.
采用单链聚合酶链反应(PCR)和测序法检测肿瘤组织中VHL基因的突变情况。
Mutation of VHL gene from tumor tissue was detected from tumor tissue by polymerase chain reaction (PCR) and direct sequencing.
方法采用逆转录聚合酶链反应(RT -PCR)检测84例静脉毒瘾者血浆标本。
Methods HGV RNA in plasma of 84 IVDUs was detected by reverse transcription polymerase chain reaction (RT PCR).
采用聚合酶链反应（PCR）技术和光密度扫描检测两组线粒体DNA的缺失突变情况。
Deletion mutation state of the two groups of mitochondria DNA were detected by PCR technology and photodensity scan.
目的：用荧光定量聚合酶链反应(FQ - PCR)测定丙型肝炎病毒在临床的应用。
Objective To investigate the clinical application of the Fluorescence quantitative PCR (FQ-PCR) in the detection of HCV infection.
目的探讨荧光定量聚合酶链反应(FQ - PCR)在巨细胞病毒性肝炎中的应用价值。
Objective To investigate the fluorescence quantitative polymerase chain reaction (FQ-PCR) in the giant cell viral hepatitis in value.
有各种逆转录酶聚合酶链反应(扩增核糖核酸基因组RT–PCR)检测试验方法，但灵敏度各不相同。
Various reverse transcriptase–polymerase chain reaction (RT–PCR) methods are available but are of variable sensitivity.
大多数分子标记体系的利用都取决于聚合酶链反应（PCR），这是一项扩增特定DNA序列的重要技术。
Use of most molecular marker systems depends on the polymerase chain reaction (PCR), which is an important technique for amplifying specific DNA sequences.
应用聚合酶链反应得到2株蓝绿藻的毒素聚酮合成酶(PKS)基因，并进行基因序列分析。
Gene of polyketide synthase (PKS) from 2 toxin-producing cyanobacteria was prepared by polymerase chain reaction and the gene sequence was analyzed.
需要使用包括聚合酶链反应（PCR），琼脂糖凝胶电泳，探针的标记与检测等生物工程技术。
This technique employs standard operations of biomedical engineering, such as polymerase chain reaction(PCR), agarose gel electrophoresis, labeling and detecting of probe.
目的建立套式聚合酶链反应（PCR）加限制性酶切分析方法检测人巨细胞病毒（HCMV）。
Objectives To establish an nested (polymerase chain reaction) PCR analytic method with restrictive enzyme to detect human cytomegalovirus (HCMV) rapidly in clinics.
方法提取人外周血单个核细胞总RNA，反转录聚合酶链反应（RT-PCR）扩增目的基因；
Methods RNA from human peripheral blood mononuclear cells were extracted and target genes were amplified by RT-PCR.
方法提取人外周血单个核细胞总RNA，反转录聚合酶链反应（RT-PCR）扩增目的基因；
Methods RNA from human peripheral blood mononuclear cells were extracted and target genes were amplified by RT-PCR.
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