نمایش مختصر رکورد

dc.contributor.authorMovafagh, Abolfazlen_US
dc.contributor.authorHeydary, Hassanen_US
dc.contributor.authorMortazavi-Tabatabaei, Seyed AbdolRezaen_US
dc.contributor.authorAzargashb, Eznollahen_US
dc.date.accessioned1399-07-09T06:58:44Zfa_IR
dc.date.accessioned2020-09-30T06:58:44Z
dc.date.available1399-07-09T06:58:44Zfa_IR
dc.date.available2020-09-30T06:58:44Z
dc.date.issued2011-12-01en_US
dc.date.issued1390-09-10fa_IR
dc.date.submitted2011-09-18en_US
dc.date.submitted1390-06-27fa_IR
dc.identifier.citationMovafagh, Abolfazl, Heydary, Hassan, Mortazavi-Tabatabaei, Seyed AbdolReza, Azargashb, Eznollah. (2011). The Significance Application of Indigenous Phytohemagglutinin (PHA) Mitogen on Metaphase and Cell Culture Procedure. Iranian Journal of Pharmaceutical Research, 10(4), 895-903. doi: 10.22037/ijpr.2011.1008en_US
dc.identifier.issn1735-0328
dc.identifier.issn1726-6890
dc.identifier.urihttps://dx.doi.org/10.22037/ijpr.2011.1008
dc.identifier.urihttp://ijpr.sbmu.ac.ir/article_1008.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/313146
dc.description.abstractPhytohemagglutinin (PHA) is a lectin, obtained from the red kidney bean that binds to the membranes of T-cells and stimulates metabolic activity, cell division, etc. The object of this research was the comparison between self made PHA (Indigenous) and imported commercial one, following conventional and High Resolution Cell Synchronization technique (HRCS) .From each blood sample of healthy individual donor replicate cell culture with two different PHA (self-made and commercial imported) with same concentration were cultured simultaneously. For culture cells, 3-5 × 1066 cells were cultured in 4 mL medium( RPMI 1640 supplemented with 15 per cent heat inactivated fetal bovine serum, 0.1 mL Phytohemagglutinin was added and kept at 37°C in an atmosphere containing 5% CO2. The processing of mitotic division from 48 h and 72 h cultures was performed according to the standard and High Resolution Cell Synchronization technique. Cytogenetic studies were performed in 100 normal healthy blood donor individuals. Statistical analysis was performed by SPSS (version 16, Inc.USA) software.Our results indicate that the preparation of fresh Phytohemagglutinin at the time of cell division and cell culture procedure reveals satisfactory score. The overall frequency of mitotic index in our study was better when compared with commercial imported Phytohemagglutinin (p < 0.001).The significant differences in the results may be due to fresh preparation. However, cost effective, easy and nearest approach of this indigenous product and high demand for this product among health care services can be considered.en_US
dc.format.extent1398
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherSchool of Pharmacy, Shahid Beheshti University of Medical Sciencesen_US
dc.relation.ispartofIranian Journal of Pharmaceutical Researchen_US
dc.relation.isversionofhttps://dx.doi.org/10.22037/ijpr.2011.1008
dc.subjectApplicationen_US
dc.subjectcell cultureen_US
dc.subjectIndigenousen_US
dc.subjectMitotic indexen_US
dc.subjectPhytohemagglutinin (PHA)en_US
dc.titleThe Significance Application of Indigenous Phytohemagglutinin (PHA) Mitogen on Metaphase and Cell Culture Procedureen_US
dc.typeTexten_US
dc.typeResearch articleen_US
dc.contributor.departmentDepartment of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran.en_US
dc.contributor.departmentDepartment of Medical Anatomy, Shahid Beheshti University of Medical Sciences. Tehran, Iran.en_US
dc.contributor.departmentProteomics Research Center, Facalty of School of Paramedical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.en_US
dc.contributor.departmentDepartment of Medical Health Community, Shahid Beheshti University of Medical Sciences, Tehran, Iran.en_US
dc.citation.volume10
dc.citation.issue4
dc.citation.spage895
dc.citation.epage903


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