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L ab M ed Clin N ovem ber V ol N o
C y clin E R N A
CyclinE RNA U
RT PCR mRNA CyclinE
CyclinE RNA
Lipofectamine U
RT PCR CyclinEmRNA
CyclinE RNA PCyclinE PCyclinE PCyclinE PCyclinE CyclinEmRNA
CyclinE RNA Cy
clinE RNA U CyclinE mRNA
RNA E
DOI 10 3969 issn2014 21 006 A
j
Construction of new target eukaryotic expression vectors of CyclinE siRNA QU Zhiz hen L I U Shan WA N G Y an
y an GA O N aik ang H U Gej ile Dep artment of L abo ratory M e dic ine Dep artment of N euros urge ry A f
f iliate d H osp ital of N eimengg u M e dical Univ e rs ity H uhehaote N e imeng g u China
Abstract Objective T o construct the new targets eukaryotic ex pression vectors of human CyclinE interf er
ence specific RNA to transf ect into glioma U cells the mRNA ex pression w as detected by RT PCR for obtaining
the ukaryo tic ex pression vectors w ith the best interf erence effect to provide the valuable data for Cyclin E becoming
the human tumor marker Methods Four new targets eukaryotic ex pression vectors of RNA interf erence specific
CyclinE w ere constructed named as PCyclinE PCyclinE PCyclinE and PCyclinE T he double digestion method and the base
sequence measuring w ere adopted to detect w hether the vectors w ere successf ully constructed T he four new ly
constructed vectors w ere transfected into U cell line by Lipofectamine T he RT PCR results w as adopted
to detect the ex pression quantity of CyclinE mRNA for selecting a vector w ith best interf erence Results new
targets eukaryotic ex pression vectors of RNA interference specific for CyclinE w ere constructed CyclinEmRNA
w as obviously suppressed the eukaryotic expression vector w ith best interference effec
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