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核糖体展示技术的原理与应用 被引量:4

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出处 《中华微生物学和免疫学杂志》 CAS CSCD 北大核心 2002年第5期582-586,共5页 Chinese Journal of Microbiology and Immunology
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参考文献39

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  • 2Sabine J, Katja MA, Kristan M, et al. Selectively infective phage (SIP) technology: scope and limitations. J Immunol Methods, 1999, 231(1-2): 93-104.
  • 3Hanes J, Pluckthun A. In vitro selection and evolution of functional proteins by using ribosome display. Proc Natl Acad Sci USA, 1997, 94(10): 4937-4942.
  • 4Mattheakis LC, Bhatt RR, Dower WJ. An in vitro polysome display system for identifying ligands from very large peptide libraries. Proc Natl Acad Sci USA, 1994, 91(19): 9022-9026.
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同被引文献66

  • 1田志坚,张学文.体外分子展示技术[J].生命的化学,2004,24(6):518-520. 被引量:1
  • 2袁青,夏玉先,殷幼平,胡浩,王中康.文库筛选与分子进化的核糖体展示新方法[J].中国生物化学与分子生物学报,2005,21(6):732-736. 被引量:3
  • 3张永钢,李振莉.DNA展示技术的原理及应用[J].国际生物制品学杂志,2006,29(3):126-129. 被引量:1
  • 4张万巧,王建,贺福初.mRNA展示技术[J].生物化学与生物物理进展,2006,33(8):795-799. 被引量:3
  • 5黄志伟,王琰.抗体工程[M].第二版.北京:北京医科大学出版社,2002.
  • 6DOWER WJ,MATFHEAKIS LC.In vitro selection as a powerful tool for the applied evolution of proteins and peptides.[J].Curr Opin Chem Biol,2002,6(3):390—398.
  • 7WITTRUP KD.Phage on display[J].Trends Biotechnol,1999,17(11):423—424.
  • 8KREBBER C,SPADA S,DESPLANCQ D,et al.Selectively—infective phage(SIP):a mechanistic dissection of a novel in vivo selection for protein-ligand interactions[J].J Mol Biol,1997,268(3):607—618.
  • 9HOOGENBOOM HR,DE BRUINE AP,HUFTON SE,et al.Antibody phage display technology and its applications[J].Immunoteehnology,1998,4(1):1—20.
  • 10HANES J.PLUCKTHUN A.In vitro selection and evolution of functional proteins by using ribosome display[J].Proc Nail Acad Sci,1997,94(10):4937—4942.

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