WB
Western blot analysis of Alpha 1 Acid Glycoprotein on different lysates with Mouse anti-Alpha 1 Acid Glycoprotein antibody at 1/1,000 dilution.
Lane 1: HepG2 cell lysate (20 µg/Lane),
Lane 2: HeLa cell lysate (20 µg/Lane),
Lane 3: THP-1 cell lysate (20 µg/Lane),
Lane 4: HCT 116 cell lysate (20 µg/Lane),
Lane 5: 293T cell lysate (20 µg/Lane),
Lane 6: NIH:OVCAR-3 cell lysate (20 µg/Lane),
Lane 7: Human liver tissue lysate (40 µg/Lane),
Exposure time: 1 minute 59 seconds;
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 at 1/1,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.
IHC
Immunohistochemical analysis of paraffin-embedded rat liver tissue using anti- Alpha-1-acid glycoprotein antibody. Counter stained with hematoxylin.
IHC
Immunohistochemical analysis of paraffin-embedded human lung cancer tissue using anti-Alpha-1-acid glycoprotein antibody. Counter stained with hematoxylin.
IHC
Immunohistochemical analysis of paraffin-embedded human esophagus tissue using anti-Alpha-1-acid glycoprotein antibody. Counter stained with hematoxylin.
FC
Flow cytometric analysis of HepG2 cells with Alpha-1-acid glycoprotein antibody at 1/100 dilution (purple) compared with an unlabelled control (cells without incubation with primary antibody; yellow). Alexa Fluor 488-conjugated goat anti-rabbit IgG was used as the secondary antibody.