Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
Immunofluorescence (IF): | 1:50-400 |
(Boiling the paraffin sections in 10mM citrate buffer,pH6.0,or PH8.0 EDTA repair liquid for 20 mins is required for the staining of formalin/paraffin sections.) Optimal working dilutions must be determined by end user. |
Western blot analysis of ACC1/ACACA using anti-ACC1/ACACA antibody (AZA0A8M6YZ52). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: zebrafish head tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ACC1/ACACA antigen affinity purified polyclonal antibody (AZA0A8M6YZ52) 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 ACC1/ACACA at approximately 269 kDa. The expected band size for ACC1/ACACA is at 269 kDa.
IHC analysis of ACC1/ACACA using anti-ACC1/ACACA antibody (AZA0A8M6YZ52).
ACC1/ACACA was detected in a paraffin-embedded section of zebrafish liver tissue. The tissue section was incubated with rabbit anti-ACC1/ACACA Antibody (AZA0A8M6YZ52) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of ACC1/ACACA using anti-ACC1/ACACA antibody (AZA0A8M6YZ52).
ACC1/ACACA was detected in a paraffin-embedded section of zebrafish ovary tissue. The tissue section was incubated with rabbit anti-ACC1/ACACA Antibody (AZA0A8M6YZ52) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IF analysis of ACC1/ACACA using anti-ACC1/ACACA antibody (AZA0A8M6YZ52).
ACC1/ACACA was detected in a paraffin-embedded section of zebrafish embryo tissue. The tissue section was incubated with rabbit anti-ACC1/ACACA Antibody (AZA0A8M6YZ52) 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 ACC1/ACACA using anti-ACC1/ACACA antibody (AZA0A8M6YZ52). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: zebrafish head tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ACC1/ACACA antigen affinity purified polyclonal antibody (AZA0A8M6YZ52) 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 ACC1/ACACA at approximately 269 kDa. The expected band size for ACC1/ACACA is at 269 kDa.
IHC analysis of ACC1/ACACA using anti-ACC1/ACACA antibody (AZA0A8M6YZ52).
ACC1/ACACA was detected in a paraffin-embedded section of zebrafish liver tissue. The tissue section was incubated with rabbit anti-ACC1/ACACA Antibody (AZA0A8M6YZ52) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of ACC1/ACACA using anti-ACC1/ACACA antibody (AZA0A8M6YZ52).
ACC1/ACACA was detected in a paraffin-embedded section of zebrafish ovary tissue. The tissue section was incubated with rabbit anti-ACC1/ACACA Antibody (AZA0A8M6YZ52) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IF analysis of ACC1/ACACA using anti-ACC1/ACACA antibody (AZA0A8M6YZ52).
ACC1/ACACA was detected in a paraffin-embedded section of zebrafish embryo tissue. The tissue section was incubated with rabbit anti-ACC1/ACACA Antibody (AZA0A8M6YZ52) 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).