Anti-PDHA1 antibody [EPR11099] - BSA and Azide free

• Flow Cyt (Intra)

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Flow Cytometry (Intracellular) - Anti-PDHA1 antibody [EPR11099] - BSA and Azide free (AB249188)

This data was developed using ab155096, the same antibody clone in a different buffer formulation.Overlay histogram showing HeLa cells stained with ab155096 (red line). The cells were fixed with 80% methanol (5 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 (ab155096, 1/10000 dilution) for 30 min at 22°C. The secondary antibody used was Alexa Fluor^® 488 goat anti-rabbit IgG (H&L) (ab150077) at 1/2000 dilution for 30 min at 22°C. Isotype control antibody (black line) was rabbit IgG (monoclonal) (0.1μg/1x10⁶ cells) used under the same conditions. Unlabelled sample (blue line) was also used as a control. Acquisition of >5,000 events were collected using a 20mW Argon ion laser (488nm) and 525/30 bandpass filter.

• IHC-P

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Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PDHA1 antibody [EPR11099] - BSA and Azide free (AB249188)

This data was developed using ab155096, the same antibody clone in a different buffer formulation.Immunohistochemical analysis of paraffin-embedded Human thyroid carcinoma tissue labeling PDHA1 with ab155096 at 1/50 dilution. Perform heat mediated antigen retrieval before commencing with IHC staining protocol.

• WB

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Western blot - Anti-PDHA1 antibody [EPR11099] - BSA and Azide free (AB249188)

This data was developed using ab155096, the same antibody clone in a different buffer formulation.

All lanes:

Western blot - Anti-PDHA1 antibody [EPR11099] (<a href='/en-us/products/primary-antibodies/pdha1-antibody-epr11099-ab155096'>ab155096</a>) at 1/1000 dilution

Lane 1:

HepG2 cell lysate at 10 µg

Lane 2:

293T cell lysate at 10 µg

Lane 3:

HeLa cell lysate at 10 µg

Lane 4:

Jurkat cell lysate at 10 µg

Secondary

All lanes:

Goat anti-rabbit HRP conjugated at 1/2000 dilution

Predicted band size: 43 kDa

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• WB

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Western blot - Anti-PDHA1 antibody [EPR11099] - BSA and Azide free (AB249188)

This data was developed using ab155096, the same antibody clone in a different buffer formulation.

Lanes 1 - 3 : Merged signal (red and green). Green - ab155096 observed at 43 kDa. Red - loading control, ab130007, observed at 130 kDa.

ab155096 was shown to recognize PDHA1 in wild-type HeLa cells as signal was lost at the expected MW in PDHA1 knockout cells. Additional cross-reactive bands were observed in the wild-type and knockout cells. Wild-type and PDHA1 knockout samples were subjected to SDS-PAGE. The membrane was blocked with 3% Milk. ab155096 and ab130007 (Mouse anti-Vinculin loading control) were incubated overnight at 4°C at 1/1000 dilution and 1/20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye^® 800CW) preabsorbed ab216773 and Goat anti-Mouse IgG H&L (IRDye^® 680RD) preabsorbed ab216776 secondary antibodies at 1/20000 dilution for 1 hour at room temperature before imaging.

All lanes:

Western blot - Anti-PDHA1 antibody [EPR11099] (<a href='/en-us/products/primary-antibodies/pdha1-antibody-epr11099-ab155096'>ab155096</a>) at 1/1000 dilution

Lane 1:

Wild-type HeLa whole cell lysate at 20 µg

Lane 2:

PDHA1 knockout HeLa whole cell lysate at 20 µg

Lane 3:

HEK-293 whole cell lysate at 20 µg

Predicted band size: 43 kDa

Observed band size: 43 kDa

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• ICC/IF

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Immunocytochemistry/ Immunofluorescence - Anti-PDHA1 antibody [EPR11099] - BSA and Azide free (AB249188)

This data was developed using ab155096, the same antibody clone in a different buffer formulation.

Immunofluorescent analysis of HeLa cells labeling PDHA1 with ab155096 at 1/250 dilution.