Anti-PPP1R1A antibody [EP902Y] - BSA and Azide free

• IHC-P

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Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PPP1R1A antibody [EP902Y] - BSA and Azide free (AB247299)

This data was developed using ab40877, the same antibody clone in a different buffer formulation.

Immunohistochemical analysis of paraffin-embedded human normal brain tissue using ab40877 diluted 1 : 100.

Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.

• Flow Cyt (Intra)

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Flow Cytometry (Intracellular) - Anti-PPP1R1A antibody [EP902Y] - BSA and Azide free (AB247299)

This data was developed using ab40877, the same antibody clone in a different buffer formulation.

Overlay histogram showing SH-SY5Y cells stained with ab40877 (red line). The cells were fixed with 4% paraformaldehyde (10 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab40877, 1/20 dilution) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-rabbit IgG (H+L) (ab96899) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was rabbit IgG (monoclonal) (1μg/1x10⁶ cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in SH-SY5Y cells fixed with 80% methanol/permeabilized in 0.1% PBS-Tween used under the same conditions.

• ICC/IF

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Immunocytochemistry/ Immunofluorescence - Anti-PPP1R1A antibody [EP902Y] - BSA and Azide free (AB247299)

This data was developed using ab40877, the same antibody clone in a different buffer formulation.ICC/IF image of ab40877 stained PC12 cells. The cells were 100% methanol fixed (5 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab40877, 5μg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor^® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor^® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43μM.

• WB

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Western blot - Anti-PPP1R1A antibody [EP902Y] - BSA and Azide free (AB247299)

This data was developed using ab40877, the same antibody clone in a different buffer formulation.

All lanes:

Western blot - Anti-PPP1R1A antibody [EP902Y] (<a href='/en-us/products/primary-antibodies/ppp1r1a-antibody-ep902y-ab40877'>ab40877</a>) at 1/40000 dilution

All lanes:

Rat brain tissue lysate at 10 µg

Predicted band size: 19 kDa

Observed band size: 27 kDa

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