Anti CD48

Western Blot
Positive WB detected in: Jurkat whole cell lysate, Raji whole cell lysate, Daudi whole cell lysate, Mouse liver tissue
All lanes: CD48 antibody at 1:4000
Secondary
Goat polyclonal to mouse IgG at 1/50000 dilution
Predicted band size: 28, 20KDa
Observed band size: 43 KDa
Exposure time：5min

Western Blot
Positive WB detected in: 20ug Raji whole cell lysate
CD48 antibody at 1:2000, 1:4000, 1:8000, 1:16000, 1:32000, 1:64000, 1:128000
Secondary
Goat polyclonal to mouse IgG at 1/50000 dilution
Predicted band size: 28, 20 KDa
Observed band size: 43 KDa
Exposure time：5min

Immunofluorescence staining of JK cells with CSB-MA004941A0m at 1:100, counter-stained with DAPI. The cells were fixed in 4% formaldehyde and blocked in 10% normal Goat Serum. The cells were incubated with the antibody overnight at 4°C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated AffiniPure Goat Anti-Mouse IgG (H+L).

Overlay Peak curve showing JK cells stained with CSB-MA004941A0m (red line) at 1:200. The cells were incubated in 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1μg/1*106 cells) for 1h at 4°C. The secondary antibody used was FITC-conjugated Goat Anti-Mouse IgG(H+L) at 1/100 dilution for 30min at 4°C. Isotype control antibody (green line) was mouse IgG1 (1μg/1*106 cells) used under the same conditions. Acquisition of >10,000 events was performed.