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pubmed-article:15646327pubmed:abstractTextMouse colon cancer cells CT26 were transfected with constructed plasmid expressing mouse soluble B lymphocyte stimulator (msBlyS). Single cell clones were selected with 100 microg/ml Zeosin and subcloned by serial limiting dilution. Eight resistant transfectants were isolated and expanded, and five of them displayed the desirable msBlyS cDNA band amplified by semi-quantitative RT-PCR assay. Western blot analysis showed that only msBlyS molecules of the expected size were detected in the cell lysates from transfectants. The supernatant of transfectants could costimulate B cell proliferation in standard costimulation assay. Thus we have successfully screened the stable transfectants expressing high levels of msBlyS in CT26 cells, which could be used as cancer vaccines for further anti-tumor immunotherapy.lld:pubmed
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pubmed-article:15646327pubmed:authorpubmed-author:WeiYuquanYlld:pubmed
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pubmed-article:15646327pubmed:authorpubmed-author:FuChunhuaClld:pubmed
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pubmed-article:15646327pubmed:volume21lld:pubmed
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pubmed-article:15646327pubmed:pagination897-900lld:pubmed
pubmed-article:15646327pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:15646327pubmed:year2004lld:pubmed
pubmed-article:15646327pubmed:articleTitle[Screening and identification of stable transfectants of mouse soluble B lymphocyte stimulator].lld:pubmed
pubmed-article:15646327pubmed:affiliationKey Laboratory of Biotherapy of Human Diseases of Ministry of National Education and Cancer Center, West China Hospital, Sichuan University, Chengdu 610041, China.lld:pubmed
pubmed-article:15646327pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:15646327pubmed:publicationTypeEnglish Abstractlld:pubmed
pubmed-article:15646327pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed