| Western blot (WB): | 1:500-2000 |
| Immunohistochemistry (IHC): | 1:50-400 |
| Immunocytochemistry/Immunofluorescence (ICC/IF): | 1:50-400 |
| Flow Cytometry (Fixed): | 1:50-200 |

Western blot analysis of ADAR using anti-ADAR antibody (PB1028). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: HELA whole cell lysates,
Lane 2: A549 whole cell lysates,
Lane 3: MCF-7 whole cell lysates,
Lane 4: HEPG2 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ADAR antigen affinity purified polyclonal antibody (PB1028) 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 ADAR at approximately 110 kDa/150 kDa. The expected band size for ADAR is at 136 kDa.

IHC analysis of ADAR using anti-ADAR antibody (PB1028).
ADAR was detected in a paraffin-embedded section of human lung cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-ADAR Antibody (PB1028) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.

ICC/IF analysis of ADAR using anti-ADAR antibody (PB1028).
ADAR was detected in an immunocytochemical section of U2OS cells. The section was incubated with rabbit anti-ADAR Antibody (PB1028) at a dilution of 1:100. Fluoro488 Conjugated Goat Anti-Rabbit IgG (Green) (Catalog # BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).

Flow cytometry analysis of A431 cell(1:100) Fluoro488 conjugated goat anti-rabbit IgG(blue) was used as secondary antibody. Isotype control antibody (Green line) was rabbit IgG Fluoro488. Unlabelled sample (Red line).

Western blot analysis of ADAR using anti-ADAR antibody (PB1028). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: HELA whole cell lysates,
Lane 2: A549 whole cell lysates,
Lane 3: MCF-7 whole cell lysates,
Lane 4: HEPG2 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ADAR antigen affinity purified polyclonal antibody (PB1028) 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 ADAR at approximately 110 kDa/150 kDa. The expected band size for ADAR is at 136 kDa.

IHC analysis of ADAR using anti-ADAR antibody (PB1028).
ADAR was detected in a paraffin-embedded section of human lung cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-ADAR Antibody (PB1028) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.

ICC/IF analysis of ADAR using anti-ADAR antibody (PB1028).
ADAR was detected in an immunocytochemical section of U2OS cells. The section was incubated with rabbit anti-ADAR Antibody (PB1028) at a dilution of 1:100. Fluoro488 Conjugated Goat Anti-Rabbit IgG (Green) (Catalog # BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).

Flow cytometry analysis of A431 cell(1:100) Fluoro488 conjugated goat anti-rabbit IgG(blue) was used as secondary antibody. Isotype control antibody (Green line) was rabbit IgG Fluoro488. Unlabelled sample (Red line).



