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 CD63 using anti-CD63 antibody (PB9250). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human MDA-MB-453 whole cell lysates,
Lane 2: human U87 whole cell lysates,
Lane 3: human HL-60 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-CD63 antigen affinity purified polyclonal antibody (PB9250) 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 CD63 at approximately 30-60 kDa. The expected band size for CD63 is at 26 kDa.
IHC analysis of CD63 using anti-CD63 antibody (PB9250) .
CD63 was detected in a paraffin-embedded section of human bladder urothelial carcinoma tissue. The tissue section was incubated with rabbit anti-CD63 Antibody (PB9250) 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 CD63 using anti-CD63 antibody (PB9250) .
CD63 was detected in a paraffin-embedded section of human spleen tissue. The tissue section was incubated with rabbit anti-CD63 Antibody (PB9250) 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.
Western blot analysis of CD63 using anti-CD63 antibody (PB9250). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human MDA-MB-453 whole cell lysates,
Lane 2: human U87 whole cell lysates,
Lane 3: human HL-60 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-CD63 antigen affinity purified polyclonal antibody (PB9250) 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 CD63 at approximately 30-60 kDa. The expected band size for CD63 is at 26 kDa.
IHC analysis of CD63 using anti-CD63 antibody (PB9250) .
CD63 was detected in a paraffin-embedded section of human bladder urothelial carcinoma tissue. The tissue section was incubated with rabbit anti-CD63 Antibody (PB9250) 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 CD63 using anti-CD63 antibody (PB9250) .
CD63 was detected in a paraffin-embedded section of human spleen tissue. The tissue section was incubated with rabbit anti-CD63 Antibody (PB9250) 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.