Construction of a prokaryotic expression vector for apoptin and preparation of polyclonal antibody of apoptin / 南方医科大学学报
Journal of Southern Medical University
; (12): 1405-1407, 2009.
Article
en Zh
| WPRIM
| ID: wpr-268747
Biblioteca responsable:
WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To construct a prokaryotic expression vector for apoptin and prepare polyclonal antibody of apoptin.</p><p><b>METHODS</b>Apoptin gene amplified from pGEM-T/Apoptin plasmid by PCR was cloned into pET-28a (+). E.coli BL21 (DE3) was transformed by the recombinant plasmid, and apoptin protein expression induced by IPTG was analyzed by SDS-PAGE. BALB/c mice were immunized with the protein and the titer of the antibody was determined using indirect enzyme-linked immunosorbent assay (ELISA).</p><p><b>RESULTS</b>Apoptin gene was successfully cloned into pET-28a (+), and the expression of a protein with relative molecular mass of about 17 000 was identified by SDA-PAGE. After 5 immunizations of the mice with the protein, the blood antibody titer reached 1:5x10(5).</p><p><b>CONCLUSION</b>The prokaryotic expression vector for apoptin is successfully constructed and the polyclonal antibody of apoptin is obtained, which allows further functional study of apoptin.</p>
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Índice:
WPRIM
Asunto principal:
Plásmidos
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Sangre
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Expresión Génica
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Genoma
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Clonación Molecular
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Proteínas de la Cápside
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Alergia e Inmunología
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Escherichia coli
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Vectores Genéticos
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Genética
Límite:
Animals
Idioma:
Zh
Revista:
Journal of Southern Medical University
Año:
2009
Tipo del documento:
Article