Western blot (WB): | 1:500-2000 |
Immunocytochemistry/Immunofluorescence (ICC/IF): | 1:50-400 |
Western blot analysis of RUNX2 using anti-RUNX2 antibody (PB0171).
Lane 1: recombinant human RUNX2 protein 0.5ng.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-RUNX2 antigen affinity purified polyclonal antibody (PB0171) 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 RUNX2 at approximately 50 kDa.
Western blot analysis of RUNX2 using anti-RUNX2 antibody (PB0171). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: HELA whole cell lysates,
Lane 2: A431 whole cell lysates,
Lane 3: K562 whole cell lysates,
Lane 4: JURKAT whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-RUNX2 antigen affinity purified polyclonal antibody (PB0171) 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 RUNX2 at approximately 57 kDa. The expected band size for RUNX2 is at 57 kDa.
IF analysis of RUNX2 using anti-RUNX2 antibody (PB0171).
RUNX2 was detected in an immunocytochemical section of A431 cells. The section was incubated with rabbit anti-RUNX2 Antibody (PB0171) 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 RUNX2 using anti-RUNX2 antibody (PB0171).
Lane 1: recombinant human RUNX2 protein 0.5ng.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-RUNX2 antigen affinity purified polyclonal antibody (PB0171) 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 RUNX2 at approximately 50 kDa.
Western blot analysis of RUNX2 using anti-RUNX2 antibody (PB0171). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: HELA whole cell lysates,
Lane 2: A431 whole cell lysates,
Lane 3: K562 whole cell lysates,
Lane 4: JURKAT whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-RUNX2 antigen affinity purified polyclonal antibody (PB0171) 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 RUNX2 at approximately 57 kDa. The expected band size for RUNX2 is at 57 kDa.
IF analysis of RUNX2 using anti-RUNX2 antibody (PB0171).
RUNX2 was detected in an immunocytochemical section of A431 cells. The section was incubated with rabbit anti-RUNX2 Antibody (PB0171) 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).