CD73 Recombinant Rabbit Monoclonal Antibody [PSH09-57] - BSA and Azide free

This data was developed using HA723119, the same antibody clone in a different buffer formulation.
Western blot analysis of CD73 on different lysates with Rabbit anti-CD73 antibody (HA723119) at 1/2,000 dilution.

Lane 1: HT-29 cell lysate
Lane 2: U-87 MG cell lysate

Lysates/proteins at 15 µg/Lane.

Predicted band size: 63 kDa
Observed band size: 63 kDa

Exposure time: Lane 1: 3 minutes; Lane 2: 20 seconds; ECL: K1801;

4-20% SDS-PAGE gel.

Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA723119) at 1/2,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.

☑ Relative expression (RE)

This data was developed using HA723119, the same antibody clone in a different buffer formulation.
Immunocytochemistry analysis of HT-29 (positive) and HeLa (low expression) labeling CD73 with Rabbit anti-CD73 antibody (HA723119) at 1/100 dilution.

Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-CD73 antibody (HA723119) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.

Beta tubulin (HA601187, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.

This data was developed using HA723119, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of HT-29 cells labeling CD73.

Cells were washed twice with cold PBS and resuspend. Then stained with the primary antibody (HA723119, 1/5,000) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/5,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).