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Keywords: antibody
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Biochem J (2020) 477 (17): 3299–3311.
Published: 10 September 2020
.... antibody protein purification protein–protein interaction tumour necrosis factors Tumor necrosis factor alpha (TNFα) is a pleiotropic cytokine that promotes inflammation and immune response [ 1 ]. TNFα is produced by cells of the immune system as a transmembrane protein arranged in homotrimers...
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Biochem J (2013) 451 (2): e1–e3.
Published: 28 March 2013
...- and IL-13-mediated inflammatory responses to generate a novel antibody to the third ectodomain (D3) of IL-13Rα1 (IL-13 receptor α1), which forms a requisite binding site for both interleukins. This antibody potently neutralizes both IL-4 and IL-13 activities in vitro . Using X-ray crystallography...
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Biochem J (2013) 449 (1): 161–166.
Published: 07 December 2012
... an irreversible process. In the present study, we demonstrate that an active enzyme can be converted back into its zymogen form. We determined the crystal structure of uPA (urokinase-type plasminogen activator) in complex with an inhibitory antibody, revealing that the antibody ‘rezymogenizes’ already activated...
Includes: Supplementary data
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Biochem J (2011) 436 (1): 1–13.
Published: 27 April 2011
...Vincent J. B. Ruigrok; Mark Levisson; Michel H. M. Eppink; Hauke Smidt; John van der Oost Antibodies are the most successful affinity tools used today, in both fundamental and applied research (diagnostics, purification and therapeutics). Nonetheless, antibodies do have their limitations, including...
Includes: Supplementary data
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Biochem J (2010) 430 (2): 179–189.
Published: 13 August 2010
...Rajkumar Ganesan; Charles Eigenbrot; Daniel Kirchhofer Antibodies display great versatility in protein interactions and have become important therapeutic agents for a variety of human diseases. Their ability to discriminate between highly conserved sequences could be of great use for therapeutic...
Includes: Multimedia, Supplementary data
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Biochem J (2009) 417 (1): 173–184.
Published: 12 December 2008
... Mps1 phosphorylation using combined mass spectrometric, mutational and phosphospecific antibody approaches. We have identified 16 sites of Mps1 autophosphorylation in vitro , several of which are required for catalytic activity after expression in bacteria or in cultured human cells. Using novel...
Includes: Supplementary data
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Biochem J (2003) 374 (2): 443–451.
Published: 01 September 2003
...), but additional mechanisms for removal of surface-bound antibody also operate. Four Rab proteins, Tb (trypanosomal) RAB4, 5A, 5B and 11 are located to the endosomal system; TbRAB5A and TbRAB11 co-localize with internalized anti-VSG antibody and transferrin. A live cell assay was used to record a single cycle...
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Biochem J (2002) 365 (3): 889–895.
Published: 01 August 2002
...-tubulin bands were identified in microtubule protein preparations under conditions of non-denaturing electrophoresis. Immunoprecipitation experiments with monoclonal antibodies against γ-tubulin and α-tubulin revealed interactions of both γ-tubulin forms with tubulin dimers, irrespective of the size...
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Biochem J (2000) 345 (1): 25–32.
Published: 17 December 1999
... affinity to (GR-FNIII)gp130. In assays measuring differentiation the (gp130-FNIII)GR cells were fully responsive to G-CSF, whereas the (GR-FNIII)gp130 cells responded fully to the agonistic anti-gp130 monoclonal antibody (mAb) B-S12, but not to IL-6 or LIF. Neutralizing mAbs that recognize the membrane...
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Biochem J (1999) 338 (2): 529–538.
Published: 22 February 1999
... (Asn-Asn-Ser) is located at position 75 in the variable region of its heavy chain. The antibody was cleaved into its antigen-binding (Fab) and crystallizing fragments. The oligosaccharides of the Fab fragment were released by digestion with various endo - and exo glycosidases and analysed by anion...