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Our Abpromise guarantee covers the use of ab70666 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|WB||1/20000. Detects a band of approximately 22 kDa (predicted molecular weight: 22 kDa).|
|IP||Use at 7.5 µg/mg of lysate.|
|ELISA||Use at an assay dependent dilution.|
Lane 1: Wild-type HAP1 cell lysate (20 µg)
Lane 2: Peroxiredoxin knockout HAP1 cell lysate (20 µg)
Lane 3: A431 cell lysate (20 µg)
Lane 4: Jurkat cell lysate (20 µg)
Lanes 1 - 4: Merged signal (red and green). Green - ab70666 observed at 23 kDa. Red - loading control, ab181602, observed at 37 kDa.
ab70666 was shown to specifically react with Peroxiredoxin when Peroxiredoxin knockout samples were used. Wild-type and Peroxiredoxin knockout samples were subjected to SDS-PAGE. ab70666 and ab181602 (loading control to GAPDH) were diluted 1/20 000 and 1/10 000 respectively and incubated overnight at 4°C. Blots were developed with goat anti-rabbit IgG (H + L) and goat anti-mouse IgG (H + L) secondary antibodies at 1/10 000 dilution for 1 h at room temperature before imaging.
ab70666 has not yet been referenced specifically in any publications.
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"