辣椒脉斑驳病毒的多基因联合检测与鉴定
杨宏凯1(
),杨晶文1,沈建国2(),蔡伟3,高芳銮1()
),杨晶文1,沈建国2(),蔡伟3,高芳銮1()
Multi-Gene-Based PCR Detection and Identification of Chilli veinal mottle virus
YANG HongKai1(),YANG JingWen1,SHEN JianGuo2(),CAI Wei3,GAO FangLuan1()
),YANG JingWen1,SHEN JianGuo2(),CAI Wei3,GAO FangLuan1()
图6. 多基因联合检测的灵敏度
A：多基因联合检测;B：基于CP的PCR检测PCR; C：基于CI的PCR检测PCR。M：DNA分子量标准;1—8：100、10-1、10-2、10-3、10-4、10-5、10-6和10-7 ;9：阴性对照
Fig. 6. Sensitivity of the multi-gene-based PCR detection
A：Multi-gene-based PCR detection;B：assay based on CP; C：assay based on CI。Marker DNA (100 bp);1—8：Dilution concentration of 100, 10-1, 10-2, 10-3, 10-4, 10-5, 10-6, 10-7, respectively;9：Negative control (healthy plant)
