2011China Animal Husbandry & Veterinary MedicineRequires access

Construction of Anti-gentamicin Phage Display scFv Libraries,Selection and Identification

Suxia Zhang

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Abstract

In this study,we constructed a phage display antibody library specific for gentamicin(GEN) to get the anti-getamicin single chain antibody(scFv).We used the anti-gentamicin hybridoma(2A3) as a source of gene to produce full-length scFv fragment.The full-length scFv fragment was ligated into the phagemid vector pCANTAB5E.Then the phagemid was transformed to E.coli TGl cells by electroporation.The size of antibody libraries was 6.5×106.The primary phage display library was riched by stabilized antigen immunoaffinity panning with GEN-OVA conjugates.9 clones congtained insert and showed GEN-positive in phage-ELISA,which lay the foundation for further immunological analysis.

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What this paper is about

In this study,we constructed a phage display antibody library specific for gentamicin(GEN) to get the anti-getamicin single chain antibody(scFv).We used the anti-gentamicin hybridoma(2A3) as a source of gene to produce full-length scFv fragment.The full-length scFv fragment was ligated into the phagemid vector pCANTAB5E.Then the phagemid was transformed to E.coli TGl cells by electroporation.The size of antibody libraries was 6.5×106.The primary phage display library was riched by stabilized antigen immunoaffinity panning with GEN-OVA conjugates.9 clones congtained insert and showed GEN-positive in phage-ELISA,which lay the foundation for further immunological analysis.

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Available abstract

In this study,we constructed a phage display antibody library specific for gentamicin(GEN) to get the anti-getamicin single chain antibody(scFv).We used the anti-gentamicin hybridoma(2A3) as a source of gene to produce full-length scFv fragment.The full-length scFv fragment was ligated into the phagemid vector pCANTAB5E.Then the phagemid was transformed to E.coli TGl cells by electroporation.The size of antibody libraries was 6.5×106.The primary phage display library was riched by stabilized antigen immunoaffinity panning with GEN-OVA conjugates.9 clones congtained insert and showed GEN-positive in phage-ELISA,which lay the foundation for further immunological analysis.

Key concepts: Panning (audio), Phagemid, Phage display, Insert (composites), Biopanning, Molecular biology, Single-chain variable fragment, Antibody

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