Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 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 anti-B7-2/CD86 antibody (PB9251). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human Raji whole cell lysates,
Lane 2: human Daudi whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-B7-2/CD86 antigen affinity purified polyclonal antibody (PB9251) 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 B7-2/CD86 at approximately 60-80 kDa. The expected band size for B7-2/CD86 is at 38 kDa.
Western blot analysis of anti-B7-2/CD86 antibody (PB9251). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: mouse spleen tissue lysates,
Lane 2: mouse thymus tissue lysates,
Lane 3: mouse J774A.1 whole cell lysates,
Lane 4: mouse Ana-1 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-B7-2/CD86 antigen affinity purified polyclonal antibody (PB9251) 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 B7-2/CD86 at approximately 60-80 kDa. The expected band size for B7-2/CD86 is at 38 kDa.
IHC analysis of B7-2/CD86 using anti-B7-2/CD86 antibody (PB9251).
B7-2/CD86 was detected in a paraffin-embedded section of human tonsil tissue. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
Western blot analysis of anti-B7-2/CD86 antibody (PB9251). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human Raji whole cell lysates,
Lane 2: human Daudi whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-B7-2/CD86 antigen affinity purified polyclonal antibody (PB9251) 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 B7-2/CD86 at approximately 60-80 kDa. The expected band size for B7-2/CD86 is at 38 kDa.
Western blot analysis of anti-B7-2/CD86 antibody (PB9251). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: mouse spleen tissue lysates,
Lane 2: mouse thymus tissue lysates,
Lane 3: mouse J774A.1 whole cell lysates,
Lane 4: mouse Ana-1 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-B7-2/CD86 antigen affinity purified polyclonal antibody (PB9251) 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 B7-2/CD86 at approximately 60-80 kDa. The expected band size for B7-2/CD86 is at 38 kDa.
IHC analysis of B7-2/CD86 using anti-B7-2/CD86 antibody (PB9251).
B7-2/CD86 was detected in a paraffin-embedded section of human tonsil tissue. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.