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- Halothane genotypes of 61 Landrace,56 Large white and 30 Duroc were determined by PCR RFLP. 采用 PCR- RFL P方法对 6 1头长白猪、5 6头大约克猪和 30头杜洛克猪进行了氟烷基因型检测。
- Method:The genotypes of CYP2D6 of 88 patients treated with fluoxetine were analysed by PCR RFLP method. 方法:采用PCR-RFLP方法分析88例患者CYP2D6基因型,用氟西汀治疗8周,并测定患者治疗前后肝功能各项指标。
- Methods The loss of heterozygosity (LOH)of YNZ22, APC, MCC and DCC genes was examined by PCR RFLP technique in 60 IM cases. 方法 应用PCR?RFLP法检测了60 例肠化生组织中YNZ22、APC 、MCC、DCC基因杂合性缺失现象。
- Methods The gene polymorphism distribution of LRP and BCHE was observed in 38 AD patients and 40 controls with PCR RFLP methods,and was analysed relatedly as well. 方法 应用 PCR- RFL P方法 ,在 38例 AD患者和 40名正常人中观察 L RP和 BCHE基因多态性的分布 ,进行关联分析。
- Detection of ABO genotypes by simultaneous PCR RFLP method 复合PCR-RFLP技术检测ABO基因型
- Keywords type 2 Diabetes Mellitus;Apolipoprotein E;Polymerase chain reaction restriction fragment length polymorphism（PCR RFLP）;Coronary Heart Disease;Hypertension; 2型糖尿病;载脂蛋白E;聚合酶链反应-限制性片段长度多态性;冠心病;高血压;
- PRENATEL GENE DIAGNOSIS 0F HEMOPHILIA A BY PCR RFLPs ANALYSIS 应用PCR-RFLPs进行甲型血友病的产前基因诊断
- Methods The gene polymorphism of PS1 and AACT were genotyped in 123 AD cases and 140 controls with PCR methods and RFLP typing. 方法应用PCR-RFLP方法，在123例患者和140例正常人中观察AACT信号肽和PS1基因多态性的分布，进行关联分析。结果1.
- The PCR detection of karnal bunt of wheat. 小麦印度腥黑穗病菌PCR检测。
- The size of the amplified PCR product was 822 bp. PCR扩增片段大小为822bp,最小检测量为1080个HPs。
- The ermA and ermC genes were amplified by PCR. PCR检测与诱导型克林霉素耐药相关的ermA、ermC基因。
- G-LCR detected ten-fold EBs than PCR. G -LCR较PCR敏感 10倍 ;
- Analyse the genotype of the target genes using PCR. 聚合酶链反应(PCR)扩增目的基因进行基因型分析。
- C3d-P28 coding gene was amplified by PCR. 将PCR获得的补体C3d-P28 DNA序列以头尾串连的方式构建四聚体。
- RFLP Analysis of Asian Barley Parental Crosses and Evaluation. 亚洲型大麦亲本组合的RFLP检测及作图评价。
- PCR, when you need to solve a crime. 当你需要知道谁是孩子的爹时，
- Methods:Urease test and PCR were used. 方法:采用脲酶实验及PCR方法检测幽门螺杆菌。
- PCR products were sequenced and analyzed. PCR产物测序及分析。
- It is concordant with routine PCR method. 并与常规PCR法具有很好的一致性。
- FISH and RFLP are the most labour intensive, time consuming and more expensive methods.The special PCR markers, in some degree, are effected by the content of template DNA. FISH和RFLP方法比较费时费力且花费昂贵，而特异性PCR标记又在一定程度上受模板DNA浓度的影响。
