1) PCR fingerprinting
PCR指纹
1.
Fluconazole resistance in Candida albicans assayed by PCR fingerprinting with M13 primer;
应用M13引物PCR指纹法分析假丝酵母菌氟康唑耐药性
2.
Results: Different PCR fingerprinting were seen between T.
目的 :观察红色毛癣菌和须癣毛癣菌临床分离株 DNA PCR指纹的差异 ,找出一种区分红色毛癣菌和须癣毛癣菌的基因分类方法。
2) PCR-fingerprinting
PCR指纹
1.
Results Different PCR-fingerprinting was seen between T.
目的 用PCR方法扩增红色毛癣菌和须癣毛癣菌临床分离株的DNA ,观察PCR指纹的差异以及基因型与传统表型的关系 ,建立一种红色毛癣菌分子生物学鉴定方法。
3) PCR fingerprinting
PCR指纹图
1.
Screening for Yersinia pestis species-specific probes by PCR fingerprinting;
PCR指纹图技术筛选鼠疫耶尔森菌种特异性探针的研究
4) PCR fingerprinting
PCR指纹图谱
1.
PCR fingerprintings of cyanobacteria isolated from coralloid roots of Cycads (Cycas revoluta) and their surrounding soil;
苏铁珊瑚状根及根周围土壤中蓝细菌的PCR指纹图谱
5) ERIC-PCR fingerprinting
ERIC-PCR指纹图谱
1.
Analysis of the microbial community structure of a Spiral up-flow reactor (SUFR) at low temperature by ERIC-PCR fingerprinting;
ERIC-PCR指纹图谱技术对低温下SUFR反应器中菌群结构分析
2.
The changes in microbial community structure of the Spiral Up-Flow Reactor(SURF) during its function recovery were analyzed by ERIC-PCR fingerprinting.
使用ERIC-PCR指纹图谱技术对SUFR反应器恢复运行后的菌群结构进行分析。
3.
According to the relationship between the major pollutants removal effect and the microbial community structure,which was investigated by ERIC-PCR fingerprinting,it was found that Pontederia cordata L had obvious effect on the pollutant removal,the removal efficiencies of CODCr,NH3-N and TP being 19.
为探究引入植物对生物净化槽处理黑臭河水的影响及机理,结合水质理化指标的动态变化,采用了ERIC-PCR指纹图谱技术来分析生物净化槽内的微生物群落结构在植物不同生长阶段的变化特征,比较植物与填料不同工艺组合对微生物群落结构的影响。
6) BOX-PCR fingerprinting
BOX-PCR指纹图谱
1.
were characterized by numerical taxonomy, 16S rDNA PCR-RFLP analysis and BOX-PCR fingerprinting to describe the phenotypic and genetic diversity.
【方法】采用表型数值分类、16SrDNAPCR-RFLP分析和BOX-PCR指纹图谱分析的方法对北方地区的甘草根瘤菌进行表型、遗传多样性分析。
补充资料：immune PCR
分子式：
CAS号：
性质： 通过应用一个对DNA和抗体具双重结合活性的接连分子使作为标志物的DNA分子特异地结合到抗原-抗体复合物上，从而形成一种特异性抗原-抗体-DNA复合物。附着的DNA标志物可用适当的引物进行PCR扩增。特异性PCR产物的存在证明DNA标志物分子特异性地附着于抗原-抗体复合物上，进而证明有抗原存在。目前最为敏感的检测方法，理论上可测得一个抗原分子的存在。
CAS号：
性质： 通过应用一个对DNA和抗体具双重结合活性的接连分子使作为标志物的DNA分子特异地结合到抗原-抗体复合物上，从而形成一种特异性抗原-抗体-DNA复合物。附着的DNA标志物可用适当的引物进行PCR扩增。特异性PCR产物的存在证明DNA标志物分子特异性地附着于抗原-抗体复合物上，进而证明有抗原存在。目前最为敏感的检测方法，理论上可测得一个抗原分子的存在。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条