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禽反转录病毒特异性蛋白抗原表位筛选

Abstract第3-6页
摘要第7-15页
List of abbreviations and Symbols第15-18页
CHAPTER ONE LITERATURE REVIEW第18-34页
    1.1 Avian Leukosis virus第18-24页
        1.1.1 Historical background and Taxonomy第18-19页
        1.1.2 Avian leukosis virus envelope subgroups第19页
        1.1.3 Virus structure and replication第19-20页
        1.1.4 Pathogenesis of ALV induced diseases第20-21页
            1.1.4.1 Slowly Transforming ALV第20-21页
            1.1.4.2 Acutely Transforming ALV第21页
        1.1.5 Diagnosis of Avian leukosis第21-22页
        1.1.6 Transmission of ALV infection第22-23页
        1.1.7 Epidemiology and Control of ALV第23-24页
    1.2 Reticuloendothelial virus第24-29页
        1.2.1 Diseases caused by REV第24页
        1.2.2 Virus structure and replication第24-25页
        1.2.3 Pathogenesis of REV induced diseases第25-26页
            1.2.3.1 Nondefective REV第25-26页
            1.2.3.2 Defective Strain T REV第26页
        1.2.4 Diagnosis of REV infections第26-27页
        1.2.5 Transmission of REV infections第27页
        1.2.6 Epidemiology and Control第27-29页
    References第29-34页
CHAPTER TWO Epitope Mapping第34-57页
    2.1 Background第34页
    2.2 B-cell epitopes第34-36页
    2.3 Epitope Mapping Methods第36-46页
        2.3.1 Structural approach第36-37页
        2.3.2 Functional approach第37-46页
    2.4 Applications of epitope mapping第46-49页
        2.4.1 Immunodiagnostics applications第46-47页
        2.4.2 Peptide-based synthetic vaccines第47-49页
    References第49-57页
CHAPTER THREE Identification of a Novel Linear B-cell epitope in the p27 of AvianLeukosis Virus第57-89页
    3.1 Introduction第58-62页
    3.2 Materials and Methods第62-71页
        3.2.1 Viruses, cells and antibodies第62-63页
        3.2.2 Specificity of ALV J p27-specific monoclonal antibody第63页
        3.2.3 PCR and PCR conditions第63-65页
        3.2.4 DNA fragments recovery第65-66页
        3.2.5 Ligation and Transformation into DH5a第66-68页
        3.2.6 Construction recombinant expression vector第68页
        3.2.7 Expression of proteins第68-69页
        3.2.8 SDS-PAGE analysis第69页
        3.2.9 Western blotting analysis第69-70页
        3.2.10 Indirect ELISA第70页
        3.2.11 Homology analysis第70-71页
    3.3 Results第71-81页
        3.3.1 Indirect immunofluorescent assay (IFA)第71页
        3.3.2 PCR amplification of overlapping fragments第71-72页
        3.3.3 SDS-PAGE and Western blotting第72-76页
        3.3.4 Indirect ELISA第76-78页
        3.3.5 Epitope is highly conserved epitope among all ALV Strains第78-81页
    3.4 Discussion第81-85页
    References第85-89页
CHAPTER FOUR Identification of Two Conserved B-cell epitopes in the gp90 ofReticuloendothelial Virus using Peptide Microarray第89-111页
    4.1 Introduction第90-94页
    4.2 Materials and Methods第94-97页
        4.2.1 Viruses, cells and antibodies第94页
        4.2.2 Specificity of REV gp90 specific monoclonal antibodies第94-95页
        4.2.3 Peptides第95页
        4.2.4 Immunoassay第95-96页
        4.2.5 Data analysis第96页
        4.2.6 Indirect ELISA第96-97页
        4.2.7 Conservation of the epitope-containing sequences in REVstrains第97页
    4.3 Results第97-102页
        4.3.1 Indirect immunofluorescent assay (IFA)第97-98页
        4.3.2 Mapping epitopes by peptide microarray第98-100页
        4.3.3 Indirect ELISA第100-101页
        4.3.4 Epitopes are highly conserved epitopes among all REV Strains第101-102页
    4.4 Discussion第102-106页
    References第106-111页
CONCLUSIONS第111-112页
List of Publications第112-113页
Acknowledgements第113-115页

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