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1.Conclusions The universal primer(CHS1 1S,CHS1 1R)is regarded as a specificity primer. The result showed that the sensitivity of universal primer PCR is 100 fg.
结论皮肤病原真菌通用引物(CHS1 1S,CHS1 1R)具有较强的特异性,敏感度为100 fg;收藏指正
2.Amplification and Orientation of Dengue 2 Virus Partial E Gene Insert in pUC18 by Universal Primer Directed PCR.
通用引物PCR分离登革病毒2型cDNA及其插入方向鉴定收藏指正
3.The Study of Preparing Probes for Fluorescence in situ Hybridization (FISH) from YAC Clones by Universal Primer PCR
用万能引物PCR法从YAC中分离制备荧光原位杂交探针的研究收藏指正
4.Sensitivity determination of universal primer PCR: Seven samples ranging from 100 ng to 100 fg shown positive,except the 10 fg sample yielding negative band.
皮肤病原真菌通用引物PCR敏感性测定,模板DNA 100 ng~100 fg的7个系列浓度均扩增出了阳性条带,10 fg为阴性。收藏指正
5.Methods To amplify the class1,2 and 3 integrase genes in 184 gram negative bacilli from medistream urine by polymerase chain reaction with universal primer of 3 genes.
方法用1、2、3类三种整合酶基因通用引物扩增184株中段尿中分离革兰阴性杆菌的相应基因;收藏指正
6.A simple and efficient method, universal primer PCR (UP PCR) is described, that permits preparing DNA probes for FISH from a trace amount of YAC DNA for which sequence does not need to be known. That is, Linking the annealed UP-Linker to the YAC DNA digested with Alu Ⅰ after isolation by pulse field gel electrophresis (PFGE), then amplifying and labelling the YAC DNA by PCR using universal primer (UP).
报道了一种从微量且未知碱基顺序的YAC DNA中制备FISH探针的新方法——万能引物PCR(UP PCR),即把复性后的UP-Linker连接于PFGE分离后经Alu Ⅰ酶切的YAC DNA上,再用UP对其进行PCR扩增和标记。收藏指正
7.Polymerase Chain Reaction ( PCR) amplification of the internal transcribed spacer (ITS) of the ribosomal DNA of ?Plasmodiophora brassicae? extracting from cruciferae (Chinese cabbage, cauliflower, broccoli) have done with universal primer ITS1 and ITS4, and the PCR products were cloned into pGEM-T vector.
应用真菌核糖体基因ITS区段通用引物ITS1和ITS4,对十字花科蔬菜根肿病菌(Plasmodiophorabrassicae)rDNA进行PCR扩增,并将扩增到的目的片段克隆到pGEM-T载体上。收藏指正
8.5. Based upon the comparison of Cyto b gene sequences in 15 deer species downloaded from GenBank,a universal primer set L15774/HSF21 was used as positive control of the template quality,at the meantime,two species specific primer sets DF/DR and CF/CR were desgined to identify red deer (Cervus elaphus),sika deer (Cervus nippori) and roe deer (Capreolus capreolus) from other species.
5.经过对来自GenBank中的15种鹿类动物的Cyto b基因序列的比较,用通用引物L15774和HSF21作为模板的质量控制,设计了特异性引物DF/DR和CF/CR来鉴定马鹿、梅花鹿、狍;收藏指正
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