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dc.contributor.authorFarhadi, B
dc.contributor.authorkhaniani, MS
dc.contributor.authorDerakhshan, SM
dc.date.accessioned2018-08-26T08:51:08Z
dc.date.available2018-08-26T08:51:08Z
dc.date.issued2013
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/53263
dc.description.abstractPurpose: Various cytokine regulates hematopoesis; they promote number of stages in stem cells biology such as proliferation, differentiation and endurance. Biological effects of SCF, as a hematopoietic cytokine; is triggered by binding to its ligand c-kit. Potential therapeutic applications of SCF include hematopoietic stem cell mobilization, exvivo stem/progenitor cell expansion, gene therapy, and immunotherapy. In this study we tried to construct of pPIC9 recombinant vector containing human SCF. Methods: hSCF cDNA was amplified by PCR and both hSCF cDNA and pPIC9 as yeast expression vector (shuttle vector) digested by EcoR I and Xho I restriction enzymes. Subsequent the digestion reaction, ligation reaction was carried out. In order to verifying of pPIC9 recombinant vector containing hSCF, PCR and sequence analysis was performed. Results: The construction of recombinant expression vector of pPIC9 containing hSCF cDNA was confirmed by sequencing method successfully. Conclusion: rhSCF/pPIC9 vector can be transformed into the Picha pastoris yeast as a eukaryotic host in order to produce human SCF at industrial scale. é 2013 by Tabriz University of Medical Sciences.
dc.language.isoEnglish
dc.relation.ispartofAdvanced Pharmaceutical Bulletin
dc.subjectcomplementary DNA
dc.subjectstem cell factor
dc.subjectarticle
dc.subjectcytokine production
dc.subjectdrug manufacture
dc.subjectdrug synthesis
dc.subjectexpression vector
dc.subjecthuman
dc.subjectmolecular cloning
dc.subjectnonhuman
dc.subjectnonviral gene delivery system
dc.subjectnucleotide sequence
dc.subjectPichia pastoris
dc.subjectpolymerase chain reaction
dc.subjectsequence analysis
dc.subjectshuttle vector
dc.titleConstruction of pPIC9 recombinant vector containing human stem cell factor
dc.typeArticle
dc.citation.volume3
dc.citation.issue2
dc.citation.spage303
dc.citation.epage308
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.5681/apb.2013.049


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