Cytokeratin 20 Antibody (10A2) - Chimeric - BSA Free

Western Blot: Cytokeratin 20 Antibody (10A2) - Chimeric - BSA Free [NBP3-43568] -

Western Blot: Cytokeratin 20 Antibody (10A2) - Chimeric - BSA Free [NBP3-43568] - Human duodenum (A) (0.01µg/ml), ileum (B) (0.001µg/ml), and colon (C) (0.001µg/ml) tissue lysate (35µg protein in RIPA buffer) were resolved on an SDS-PAGE gel, and blots were probed with NBP3-43568 at the mentioned respective concentrations before detection using an anti-rabbit secondary antibody. A primary incubation of 1 hour was used, and protein was detected by chemiluminescence.

Immunocytochemistry/ Immunofluorescence: Cytokeratin 20 Antibody (10A2) - Chimeric - BSA Free [NBP3-43568] -

Immunocytochemistry/ Immunofluorescence: Cytokeratin 20 Antibody (10A2) - Chimeric - BSA Free [NBP3-43568] - Immunofluorescence analysis of paraformaldehyde fixed Caco-2 cells, permeabilized with 0.15% Triton, on coverslips stained with NBP3-43568 (1:100 dilution) for 1h followed by Alexa Fluor® 488 secondary antibody (1:1000 dilution), showing cytoplasmic staining. The nuclear stain is DAPI (blue). Panels show, from left-right, top-bottom, NBP3-43568, DAPI, merged channels, and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor® 488 secondary antibody.

Flow Cytometry: Cytokeratin 20 Antibody (10A2) - Chimeric - BSA Free [NBP3-43568] -

Flow Cytometry: Cytokeratin 20 Antibody (10A2) - Chimeric - BSA Free [NBP3-43568] - Paraformaldehyde fixed Caco-2 cells permeabilized with 0.5% Triton were stained with the anti-unknown specificity antibody (isotype control, black line) or NBP3-43568 (blue line) at a dilution of 1:100 for 1h at RT. After washing, the bound antibody was detected using a goat anti-rabbit IgG AlexaFluor® 488 antibody at a dilution of 1:1000, and the cells were analyzed using a FACSCanto flow-cytometer.