Western blot (WB): | 1:500-2000 |
Immunocytochemistry/Immunofluorescence (ICC/IF): | 1:50-400 |
Flow cytometry (FCM): | 1-3μg/1x106 cells |
Enzyme linked immunosorbent assay (ELISA): | 1:100-1000 |
Western blot analysis of TAU/MAPT using anti-TAU/MAPT antibody (A00097-3). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: rat brain tissue lysates,
Lane 2: mouse brain tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-TAU/MAPT antigen affinity purified polyclonal antibody (A00097-3) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for TAU/MAPT at approximately 50-80 kDa. The expected band size for TAU/MAPT is at 79 kDa.
IF analysis of TAU/MAPT using anti-TAU/MAPT antibody (A00097-3).
TAU/MAPT was detected in an immunocytochemical section of T-47D cells. The section was incubated with rabbit anti-TAU/MAPT Antibody (A00097-3) at a dilution of 1:100. DyLight®488 Conjugated Goat Anti-Rabbit IgG (Green) (Catalog # BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Western blot analysis of TAU/MAPT using anti-TAU/MAPT antibody (A00097-3). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: rat brain tissue lysates,
Lane 2: mouse brain tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-TAU/MAPT antigen affinity purified polyclonal antibody (A00097-3) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for TAU/MAPT at approximately 50-80 kDa. The expected band size for TAU/MAPT is at 79 kDa.
IF analysis of TAU/MAPT using anti-TAU/MAPT antibody (A00097-3).
TAU/MAPT was detected in an immunocytochemical section of T-47D cells. The section was incubated with rabbit anti-TAU/MAPT Antibody (A00097-3) at a dilution of 1:100. DyLight®488 Conjugated Goat Anti-Rabbit IgG (Green) (Catalog # BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).