Bovine β-lactoglobulin receptors on transformed mammalian cells (hybridomas MARK-3): characterization by flow cytometry
dc.contributor.author | Palupi, N.S. | |
dc.contributor.author | P. FrancK | |
dc.contributor.author | C. Guimont | |
dc.contributor.author | G. Linden | |
dc.contributor.author | D. Dumas | |
dc.contributor.author | J. Stoltz | |
dc.contributor.author | J. Stoltz | |
dc.contributor.author | P. Nabet | |
dc.contributor.author | F. Belleville-Nabe | |
dc.contributor.author | B. Dousset | |
dc.date.accessioned | 2010-06-11T08:40:59Z | |
dc.date.available | 2010-06-11T08:40:59Z | |
dc.date.issued | 2000 | |
dc.identifier.uri | http://repository.ipb.ac.id/handle/123456789/28226 | |
dc.description.abstract | Flow cytometry was used to demonstrate the presence of β-lactoglobulin (βLG) receptors on living murine hybridoma MARK-3 cells using a fluorescein isothiocyanate-βLG conjugate (FITC-βLG: molar ratio of 5:1). A site occupation curve was produced using a shift in the mean channel fluorescence at various concentrations of FITC-βLG. The binding of labelled ligand was concentration dependent and was inhibited by unlabelled βLG. The on-rate constant was 3.2×102 M−1 min−1 and the off-rate constant was 0.002 min−1. Scatchard plot analysis gave a dissociation constant (Kd) of 44±21×10−7 and 39±24×10−5 M (n=3). Flow cytometry indicated that at least 15% of the FITC-βLG were internalized for 5 min and that internalization was temperature- and time-dependent. The internalization was confirmed by 3-D fluorescence microscopy (CELLScan™ system). Author Keywords: β-Lactoglobulin; Receptor; Hybridoma; FITC; Flow cytometry | id |
dc.publisher | IPB (Bogor Agricultural University) | |
dc.title | Bovine β-lactoglobulin receptors on transformed mammalian cells (hybridomas MARK-3): characterization by flow cytometry | id |