PP2C gamma/PPM1G Antibody (JE64-91)

Western Blot: PP2C gamma/PPM1G Antibody (JE64-91) [NBP3-32844]

Western Blot: PP2C gamma/PPM1G Antibody (JE64-91) [NBP3-32844] - Western blot analysis of PP2C gamma/PPM1G on different lysates with Rabbit anti-PP2C gamma/PPM1G antibody (NBP3-32844) at 1/500 dilution.

Lane 1: 293T cell lysate, 10 ug/Lane
Lane 2: Jurkat cell lysate, 10 ug/Lane
Lane 3: Rat testis tissue lysate, 20 ug/Lane

Predicted band size: 59 kDa
Observed band size: 70 kDa

Exposure time: 2 minutes;

8% 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 (NBP3-32844) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:300,000 dilution was used for 1 hour at room temperature.

Immunohistochemistry: PP2C gamma/PPM1G Antibody (JE64-91) [NBP3-32844]

Immunohistochemistry: PP2C gamma/PPM1G Antibody (JE64-91) [NBP3-32844] - Immunohistochemical analysis of paraffin-embedded rat large intestine tissue with Rabbit anti-PP2C gamma/PPM1G antibody (NBP3-32844) at 1/100 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 (NBP3-32844) at 1/100 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.

Flow Cytometry: PP2C gamma/PPM1G Antibody (JE64-91) [NBP3-32844]

Flow Cytometry: PP2C gamma/PPM1G Antibody (JE64-91) [NBP3-32844] - Flow cytometric analysis of HepG2 cells labeling PP2C gamma/PPM1G.

Cells were fixed and permeabilized. Then stained with the primary antibody (NBP3-32844, 1ug/ml) (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 Alexa Fluor® 488 conjugate-Goat anti-Rabbit IgG Secondary antibody at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).