Abstract
Camelids produce functional antibodies devoid of light chains and constant heavy-chain domain (CH1). The antigen binding fragments of such heavy-chain antibodies are therefore comprised in one single domain, the so-called VH of the camelid heavy-chain antibody (VHH) or nanobody. The very close similarity of these molecules to human VHs illustrated the potential application of these novel products as an immunodiagnostic and immunotherapeutic reagent, so the anti-nanobody HRP conjugate is one of the key components in production, characterization, and application of these molecules in detection and therapy. These antigen-specific fragments are well expressed in Escherichia coli. Here we report high expression and purification of some nanobodies against tumor markers. The nanobody genes were subcloned into a pET22b(+) vector to overexpress the protein coupled with fusion tag in E. coli. The expressed nanobodies were purified by immobilized metal affinity chromatography and injected into rabbits as an immunogen. Described here are the preparation, purification, and characterization of anti-nanobody HRP conjugate for use in the various nanobody immunoassay systems. Several biochemical modifications were applied to increase the sensit...Continue Reading
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Sep 25, 2015·Biotechnology Progress·Yoichi KumadaJun-Ichi Horiuchi
Sep 13, 2011·Experimental Cell Research·Farnoush Jafari Iri-SoflaMohammad J Rasaee
May 16, 2021·Protein Expression and Purification·Christopher K Kariuki, Stefan Magez