
pmid: 15463931
For most expression studies focusing on the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) protein, sensitive and specific antibodies (Abs) are critically needed. Several Abs have been produced commercially or by research laboratories for CFTR detection in both cell lines with heterologous or endogenous expression and native cells/tissues. Here, we review the applicability of most Abs currently in use in CF research for the biochemical and/or immunocytochemical detection of CFTR.
Pulmonary and Respiratory Medicine, 570, Cystic Fibrosis Transmembrane Conductance Regulator, Expression, [SDV.MHEP.PSR]Life Sciences [q-bio]/Human health and pathology/Pulmonology and respiratory tract, Anti-CFTR, Antibodies, Cell Line, 618, Monoclonal, Humans, Pediatrics, Perinatology, and Child Health, MESH: Cystic Fibrosis Transmembrane Conductance Regulator, MESH: Humans, MESH: Antibodies, Immunotechniques, Antibodies, Monoclonal, MESH: Cell Line, Immunologic Techniques, [SDV.MHEP.PSR] Life Sciences [q-bio]/Human health and pathology/Pulmonology and respiratory tract, MESH: Immunologic Techniques, Western, Immunocytochemistry
Pulmonary and Respiratory Medicine, 570, Cystic Fibrosis Transmembrane Conductance Regulator, Expression, [SDV.MHEP.PSR]Life Sciences [q-bio]/Human health and pathology/Pulmonology and respiratory tract, Anti-CFTR, Antibodies, Cell Line, 618, Monoclonal, Humans, Pediatrics, Perinatology, and Child Health, MESH: Cystic Fibrosis Transmembrane Conductance Regulator, MESH: Humans, MESH: Antibodies, Immunotechniques, Antibodies, Monoclonal, MESH: Cell Line, Immunologic Techniques, [SDV.MHEP.PSR] Life Sciences [q-bio]/Human health and pathology/Pulmonology and respiratory tract, MESH: Immunologic Techniques, Western, Immunocytochemistry
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