A rapid method for detection and identification of equine herpesvirus 1 (EHV-1) and equine herpesvirus 4 (EHV-4) was developed using polymerase chain reaction (PCR).
聚合酶链反应(PCR)可作为一种快速检测并鉴别马疱疹病毒1型(EHV 1)和马疱疹病毒4型(EHV 4)的诊断方法。
To establish a new method based on scorpion primer and PCR for rapid detection of the salmonellae in environmental water samples.
以蝎形引物pcr技术为基础建立一套环境水样沙门菌的快速检测方法。
Conclusion: Immuno PCR is a highly specific and sensitive method for the detection of Toxoplasma dissoluble Antigens.
结论：免疫-P CR是一种特异性强，敏感性高的弓形虫可溶性抗原检测方法。
So the PCR method was suitable for rapid and sensitive detection of human botulism borne clostridia.
因此，此P CR方法可用于快速敏感地检测引起人类肉毒中毒的梭菌。
ObjectiveTo establish the rapid detection method of Enterotoxigenic E. coli(ETEC)by polymerase chain reaction(PCR)technology for characteristic primers.
目的利用PCR技术，尝试建立特异性引物PCR快速检测肠毒素大肠杆菌的方法。
Objective to establish RT-PCR method for Puumala virus (PUUV) detection in order to confirm existence of Puumala virus in Jilin province and analyze gene sequence of Puumala virus.
目的建立检测普马拉病毒的RT - PCR方法，确认吉林省存在普马拉病毒，并对病毒的基因片段进行分析。
Objective To establish PCR method for the detection of the asymptomatic infection of Leishmania infantum.
目的建立适合检测我国婴儿利什曼原虫无症状感染的PCR方法。
Methods:The method for MBL point mutation detection(PCR-RFLP) was Established with self-designed primers according to MBL genomic sequence;
方法：根据MBL基因序列设计引物建立MBL基因点突变检测方法即PCR -RFLP ；
Objective: To study the sensitivity of PCR method for the detection of Listeria monocytogenes in food.
目的：研究PCR检测不同食品中产单核李斯特菌的灵敏度。
A TC-RT-PCR method basing on reverse transcription with random primer facilitated the detection for those samples mixed infected by ASGV and ACLSV.
用随机引物反转录，通过TC-RT-PCR检测ACLSV和ASGV复合感染的梨样品也均获得了目标片段。
The result obtained from the detection was consistent with that from PCR analyses, indicating that the DNA chip method is reliable and effective for routine analysis of GMOs.
通过对大豆、玉米、油菜、棉花等农作物样品的检测，并由常规PCR技术进行验证，证实基因芯片的检测结果准确可靠，并提高了检测效率，因此，可用于农作物转基因背景的鉴定。
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。
It was concluded that PCR SSCP silver staining method for the detection of P53 gene mutation is quick reliable and practical.
结论：PCRSSCP银染色法是一种可靠、快速、实用的P 53基因突变检测方法。
Conclusion The method of PCR-ELISA we established for early detection and typing of all 4dengue viruses seretypes.
结论所建立的方法可用作登革病毒感染的早期诊断及分型。
This method of PCR assay appears to be simple, rapid, highly sensitive and specific, and quite valuable for the detection and surveillance of S. flexneri infection.
该方法操作简单、检验周期短、特异性和灵敏度高，能够快速地实现对食品中的志贺菌的诊检和监控。
This method of PCR assay appears to be simple, rapid, highly sensitive and specific, and quite valuable for the detection and surveillance of S. flexneri infection.
该方法操作简单、检验周期短、特异性和灵敏度高，能够快速地实现对食品中的志贺菌的诊检和监控。
应用推荐