Phospho-Bcl-2 (S70) Recombinant Rabbit Monoclonal Antibody [PSH11-02] - BSA and Azide free

☑ Cell treatment (CT)

This data was developed using HA723269, the same antibody clone in a different buffer formulation.
Western blot analysis of Phospho-Bcl-2 (S70) on different lysates with Rabbit anti-Phospho-Bcl-2 (S70) antibody (HA723269) at 1/2,000 dilution.

Lane 1: Jurrkat cell lysate
Lane 2: Jurrkat treated with 1μM paclitaxel overnight cell lysate
Lane 3: Jurrkat treated with 1μM paclitaxel overnight cell lysate, then the membrane treated with λpp for 1 hour

Lysates/proteins at 20 µg/Lane.

Predicted band size: 26 kDa
Observed band size: 26 kDa

Exposure time: 1 minute 15 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 (HA723269) at 1/2,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.

☑ Cell treatment (CT)

This data was developed using HA723269, the same antibody clone in a different buffer formulation.
Immunocytochemistry analysis of Jurkat cells untreated / treated with 1μM paclitaxel overnight labeling Phospho-Bcl-2 (S70) with Rabbit anti-Phospho-Bcl-2 (S70) antibody (HA723269) at 1/500 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-Phospho-Bcl-2 (S70) antibody (HA723269) at 1/500 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.

☑ Cell treatment (CT)

This data was developed using HA723269, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of untreated Jurkat cells (top) / Jurkat cells treated with 1μM paclitaxel overnight (bottom) labeling Phospho-Bcl-2 (S70).

Cells were fixed and permeabilized. Then stained with the primary antibody (HA723269, 1/10,000) (right) compared with Rabbit IgG Isotype Control (1μg/mL, left). 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℃.