摘要
用未纯化的呼吸道合胞病毒(RSV)细胞混和物,采用改良胍—热酚法提取病毒mRNA,反转录合成cDNA,经PCR扩增得到大小约920bp的产物。经PstⅠ酶切表明其中含有PstⅠ酶切位点,证实其产物确为RSV G基因。此法简便、特异、敏感、快速。由于RSV极不稳定,RNA甚易降解,此法值得推广应用。
From cells infected by respiratory syncytial virus (RSV),cDNA was synthesized through reverse transcription by using improved method of guanidine and heated phenol. An about 920bp product was obtained by PCR. It indicated that the product was RSV G gene because it had Pst I digestion site.
出处
《中华微生物学和免疫学杂志》
CAS
CSCD
北大核心
1995年第5期355-357,共3页
Chinese Journal of Microbiology and Immunology
基金
国家自然科学基金资助
湖北省自然科学基金资助