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dc.contributor.authorFarajnia, S
dc.contributor.authorAhmadzadeh, V
dc.contributor.authorTanomand, A
dc.contributor.authorVeisi, K
dc.contributor.authorKhosroshahi, SA
dc.contributor.authorRahbarnia, L
dc.date.accessioned2018-08-26T07:55:36Z
dc.date.available2018-08-26T07:55:36Z
dc.date.issued2014
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/48498
dc.description.abstractRecombinant antibodies are increasingly being employed as therapeutic agents especially in combination with anti-cancer drugs. The single-chain antibody fragments are small antigen-binding proteins which provide the most commonly used antibody formats for diagnostic and therapeutic purposes. These antibody fragments have more rapid tumor penetration and clearance from the serum relative to full-length monoclonal antibodies. There are in vitro antibody-display technologies such as phage display, cell surface display, ribosome display and mRNA display that can be used to isolate high specificity and affinity single-chain antibodies against a wide variety of targets. We review these strategies for generation of stable and active antibody fragments in the present article.
dc.language.isoEnglish
dc.relation.ispartofIMMUNOPHARMACOLOGY AND IMMUNOTOXICOLOGY
dc.subjectDisplay methods
dc.subjectimproved stability
dc.subjectsingle-chain antibody fragments
dc.titleDevelopment trends for generation of single-chain antibody fragments
dc.typeReview
dc.citation.volume36
dc.citation.issue5
dc.citation.spage297
dc.citation.epage308
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.3109/08923973.2014.945126


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