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標題: 傳染性華氏囊病毒的VP2蛋白 N端及C端序列對於T=1 次病毒顆粒的組裝與純化及免疫原性之影響
Effect of terminal sequences of capsid protein VP2 of infectious bursal disease virus on the formation, purification and immunogenicity of T=1 subviral particles
作者: 何靜宜
Ho, Jin-Yi
關鍵字: IBDV;傳染性華氏囊病毒;virus-like particle;truncation;IMAC;似病毒顆粒;截切;固定化金屬層析
出版社: 生物科技學研究所
引用: 林育江。2003。傳染性華氏囊病毒結構蛋白VP2之C端區域對形成次病毒顆粒及免疫力之影響。碩士論文。中興大學生物科技所。台中。 楊道翔。2005。利用昆蟲幼蟲生產傳染性華氏囊炎病毒結構蛋白VP2之次病毒顆粒及其應用。碩士論文。中興大學生物科技所。台中。 Azad, A. A., S. A. Barrett, and K. J. Fahey. 1985. The characterization and molecular cloning of the double-stranded RNA genome of an Australian strain of infectious bursal disease virus. Virology 143:35-44. Azad, A. A., M. N. Jagadish, M. A. Brown, and P. J. Hudson. 1987. Deletion mapping and expression in Escherichia coli of the large genomic segment of a birnavirus. Virology 161:145-52. Baumert, T. F., S. Ito, D. T. Wong, and T. J. Liang. 1998. Hepatitis C virus structural proteins assemble into viruslike particles in insect cells. J. Virol. 72:3827-36. Becht, H., H. M

VP2 is the structure proteins of IBDV capsid and the primary host-protective immunogen of IBDV. When expressed in insect cell, VP2-452H spontaneously forms a T=1 subviral particle (SVP). Although the structure of SVP has been determined at 2.6
其他識別: U0005-2708200617432600
Appears in Collections:生物科技學研究所

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