CD27 Recombinant Rabbit Monoclonal Antibody [PSH08-90] - BSA and Azide free

☑ Relative expression (RE)

This data was developed using HA723042, the same antibody clone in a different buffer formulation.
Western blot analysis of CD27 on different lysates with Rabbit anti-CD27 antibody (HA723042) at 1/2,000 dilution.

Lane 1: Raji cell lysate
Lane 2: Ramos cell lysate
Lane 3: MCF7 cell lysate (negative)
Lane 4: Daudi cell lysate

Lysates/proteins at 20 µg/Lane.

Predicted band size: 29 kDa
Observed band size: 55 kDa

Exposure time: 30 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 (HA723042) 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.

This data was developed using HA723042, the same antibody clone in a different buffer formulation.
Immunocytochemistry analysis of Raji cells labeling CD27 with Rabbit anti-CD27 antibody (HA723042) 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-CD27 antibody (HA723042) 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 HA723042, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human tonsil tissue with Rabbit anti-CD27 antibody (HA723042) at 1/200 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH₂O and PBS, and then probed with the primary antibody (HA723042) at 1/200 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

This data was developed using HA723042, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of human peripheral blood lymphocytes labeling CD27.

Cells were washed twice with cold PBS and resuspend. Then stained with the primary antibody (HA723042, 1μg/mL) (red) compared with Rabbit IgG Isotype Control (black). 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 1/1,000 dilution for 30 minutes at +4℃.

This data was developed using HA723042, the same antibody clone in a different buffer formulation.
CD27 was immunoprecipitated from 0.2 mg Raji cell lysate with HA723042 at 2 µg/10 µl beads. Western blot was performed from the immunoprecipitate using HA723042 at 1/1,000 dilution. Mouse Anti-Rabbit IgG kappa light chain secondary antibody (M1208-2) at 1/5,000 dilution was used for 1 hour at room temperature.

Lane 1: Raji cell lysate (input)
Lane 2: HA723042 IP in Raji cell lysate
Lane 3: Rabbit IgG instead of HA723042 in Raji cell lysate

Blocking/Dilution buffer: 5% NFDM/TBST
Exposure time: 3 minutes; ECL: K1801