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   Lentiviral Vectors Titration Using Real-Time Pcr  
   
نویسنده Allahverdi Amir ,Eskandari Fatemeh ,Moghadasi Mohammad Hossein ,Azad Mehdi ,Goudarzi Mehdi ,Abroun Saied ,Soleimani Masoud
منبع Archives Of Advances In Biosciences - 2015 - دوره : 6 - شماره : 1 - صفحه:80 -84
چکیده    Lentiviral vectors (lvs) are useful vehicle for genetransfer to dividing and non-dividing cells and genetic manipulations. however, the use of lentiviruses in studies requires an accurate titration technique.quantitative real-time pcr (qpcr) is a sensitive technique for the indication and quantitation of retrovirals particles. in this study, we used the qpcr for lentiviral vector titeration. the puromycin resistance gene as templates for an sybr green-based real-time qpcr method and detect lentiviral copy number integrated lentiviral dna. consequently, this studyshowed that theusing ofantibioticresistance genesviral particles titration maybeefficient with highly accuracy.
کلیدواژه Lentivirus; Qpcr; Titration Methods; Puromycin
آدرس Tarbiat Modares University, Faculty Of Medicine Sciences, Department Of Hematology, ایران, Tarbiat Modares University, Faculty Of Medicine Sciences, Department Of Hematology, ایران, Tarbiat Modares University, Faculty Of Medicine Sciences, Department Of Hematology, ایران, Qazvin University Of Medical Sciences, Faculty Of Allied Medicine, Department Of Medical Laboratory Sciences, ایران, Shahid Beheshti University Of Medical Sciences, School Of Medicine, Department Of Microbiology, ایران, Tarbiat Modares University, Faculty Of Medicine Sciences, Department Of Hematology, ایران, Tarbiat Modares University, Faculty Of Medicine Sciences, Department Of Hematology, ایران
 
     
   
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