Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Karin P. M. Geuijen"'
Autor:
Peter J. Simons, David F. Egging, M.H.M. Eppink, Cindy Oppers-Tiemissen, Richard B.M. Schasfoort, Karin P. M. Geuijen, Louis Boon
Publikováno v:
FEBS Open Bio
FEBS Open Bio 7 (2017) 10
FEBS Open Bio, 7(10), 1557-1574. Wiley-Blackwell
FEBS Open Bio, 7(10), 1557-1574
FEBS Open Bio 7 (2017) 10
FEBS Open Bio, 7(10), 1557-1574. Wiley-Blackwell
FEBS Open Bio, 7(10), 1557-1574
The interactions of therapeutic antibodies with fragment crystallizable γ (Fcγ) receptors and neonatal Fc receptors (FcRn) are measured in vitro as indicators of antibody functional performance. Antibodies are anchored to immune cells through the F
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33ffe397c3eccbdefcf5558847bdec48
https://doi.org/10.1002/2211-5463.12283
https://doi.org/10.1002/2211-5463.12283
Autor:
Daniëlle E. J. W. van Wijk-Basten, Michel H.M. Eppink, Karin P. M. Geuijen, Richard B.M. Schasfoort, David F. Egging
Publikováno v:
Biotechnology Journal, 12
Biotechnology journal, 12(9):1700154. Wiley-VCH Verlag
Biotechnology Journal 12 (2017)
Biotechnology journal, 12(9):1700154. Wiley-VCH Verlag
Biotechnology Journal 12 (2017)
Protein purifications are often based on the principle of affinity chromatography, where the protein of interest selectively binds to an immobilized ligand. The development of affinity purification requires selecting proper wash and elution condition
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4cae577a52d67c16211c3e7c9360f58
https://research.wur.nl/en/publications/rapid-buffer-and-ligand-screening-for-affinity-chromatography-by-
https://research.wur.nl/en/publications/rapid-buffer-and-ligand-screening-for-affinity-chromatography-by-
Publikováno v:
Analytical Biochemistry 454 (2014)
Analytical biochemistry, 454, 38-40. Academic Press
Analytical Biochemistry, 454, 38-40
Analytical biochemistry, 454, 38-40. Academic Press
Analytical Biochemistry, 454, 38-40
Affinity-based analyses on biosensors depend partly on regeneration between measurements. Regeneration is performed with a buffer that efficiently breaks all interactions between ligand and analyte while maintaining the active binding site of the lig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e618d3c52ef2c8d36ce77442bb731ca
https://doi.org/10.1016/j.ab.2014.03.011
https://doi.org/10.1016/j.ab.2014.03.011