WB
Western blot analysis of SGLT2/SLC5A2 using anti-SGLT2/SLC5A2 antibody. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human HL-60 whole cell lysates,
Lane 2: human THP-1 whole cell lysates,
Lane 3: rat kidney tissue lysates,
Lane 4: rat spleen tissue lysates,
Lane 5: rat lung tissue lysates,
Lane 6: mouse kidney tissue lysates,
Lane 7: mouse spleen tissue lysates,
Lane 8: mouse lung tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-SGLT2/SLC5A2 antigen affinity purified polyclonal antibody at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody. The signal is developed using ECL Plus Western Blotting Substrate.
IHC
IHC analysis of SGLT2/SLC5A2 using anti-SGLT2/SLC5A2 antibody.
SGLT2/SLC5A2 was detected in a paraffin-embedded section of human renal cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-SGLT2/SLC5A2 Antibody at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) with DAB as the chromogen.
IHC
IHC analysis of SGLT2/SLC5A2 using anti-SGLT2/SLC5A2 antibody.
SGLT2/SLC5A2 was detected in a paraffin-embedded section of mouse kidney tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-SGLT2/SLC5A2 Antibody at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) with DAB as the chromogen.
IHC
IHC analysis of SGLT2/SLC5A2 using anti-SGLT2/SLC5A2 antibody.
SGLT2/SLC5A2 was detected in a paraffin-embedded section of rat kidney tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-SGLT2/SLC5A2 Antibody at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) with DAB as the chromogen.
FC
Flow Cytometry analysis of HepG2 cells using anti- SLC5A2 antibody.
Overlay histogram showing HepG2 cells stained with Anti-SGLT2/SLC5A2 Antibody (Blue line).. And then incubated with rabbit anti-SLC5A2 Antibody (1:100) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (1:100) was used as secondary antibody Isotype control antibody (Green line) was rabbit IgG (1:100) used under the same conditions. Unlabelled sample (Red line) was also used as a control.