Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/5089
DC FieldValueLanguage
dc.contributor.advisorChaar, Mira Elen_US
dc.contributor.advisorTawk, Linaen_US
dc.contributor.authorNassif, Ibrahimen_US
dc.date.accessioned2021-06-17T09:14:15Z-
dc.date.available2021-06-17T09:14:15Z-
dc.date.issued2020-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/5089-
dc.descriptionIncludes bibliographical references (p. 47-53)en_US
dc.description.abstractOccult hepatitis B virus (HBV) infection (OBI) is defined as low plasma level of HBV DNA with undetectable HBV surface antigen (HBsAg). Multiple amino acid substitutions in the S protein may affect the HbsAg secretion and detection by commercial assays. In the current study, a cell culture system was optimized and will be used to study the potential role of OBI specific amino acid substitutions in the S protein. A total of 10 HBV mutants were selected from OBI blood donors. Surface gene amplification using gene specific primers were cloned in a plasmid, transformed in competent cell line and transfected in HepG2 cells. After several attempts of optimization, successful cloning method and culturing of HepG2 cell line were achieved. Optimized protocols for transfecting mutant HBsAg are currently available and will be used to study the in vitro effect of HBV amino acid substitutions.en_US
dc.description.statementofresponsibilityby Ibrahim Nassifen_US
dc.format.extent1 online resource (x, 53 pages) : ill., tablesen_US
dc.language.isoengen_US
dc.rightsThis object is protected by copyright, and is made available here for research and educational purposes. Permission to reuse, publish, or reproduce the object beyond the personal and educational use exceptions must be obtained from the copyright holderen_US
dc.subjectOccult HBV, mammalian expression system, blood donors, transfusion infections, HBsAg mutations, HepG2, cloning, transfection, transformation, S gene.en_US
dc.subject.lcshHepatitis Ben_US
dc.subject.lcshHepatitis B virusen_US
dc.subject.lcshDissertations, Academicen_US
dc.subject.lcshUniversity of Balamand--Dissertationsen_US
dc.titleMolecular cloning of HBV S-protein mutants for expression in human HepG2 liver cell lineen_US
dc.typeThesisen_US
dc.contributor.corporateUniversity of Balamanden_US
dc.contributor.departmentDepartment of Medical Laboratory Sciencesen_US
dc.contributor.facultyFaculty of Health Sciencesen_US
dc.contributor.institutionUniversity of Balamanden_US
dc.date.catalogued2021-06-17-
dc.description.degreeMS in Clinical Laboratory Sciencesen_US
dc.description.statusPublisheden_US
dc.identifier.ezproxyURLhttp://ezsecureaccess.balamand.edu.lb/login?url=http://olib.balamand.edu.lb/projects_and_theses/289773.pdfen_US
dc.identifier.OlibID289773-
dc.provenance.recordsourceOliben_US
Appears in Collections:UOB Theses and Projects
Show simple item record

Record view(s)

23
checked on Sep 22, 2022

Google ScholarTM

Check


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.