Boriskin Y S
Department of Medical Microbiology, St George's Hospital Medical School, London, UK.
New Microbiol. 2001 Jan;24(1):1-9.
A quantitative nested DNA PCR for human cytomegalovirus (CMV) was developed using PCR mimic DNA as an internal standard. A combination of ultra-thin gel and enhanced detection of ethidium bromide-stained PCR bands allowed us to achieve a 25-fold increase in sensitivity over the conventional gel electrophoreses, down to 0.1 ng of DNA per band. When the technique was applied to measuring CMV load in CMV positive leucocyte DNA preparations its sensitivity spanned the range from single to hundreds of CMV DNA copies in 0.1 microg of total white blood cell DNA.
利用PCR模拟DNA作为内标,开发了一种用于人巨细胞病毒(CMV)的定量巢式DNA PCR。超薄凝胶与溴化乙锭染色PCR条带增强检测相结合,使我们的灵敏度比传统凝胶电泳提高了25倍,低至每条带0.1 ng DNA。当该技术应用于测量CMV阳性白细胞DNA制剂中的CMV载量时,其灵敏度范围为0.1μg总白细胞DNA中从单个到数百个CMV DNA拷贝。