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 MMP8 using anti-MMP8 antibody (BA2201). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: rat PC-12 whole cell lysates,
Lane 2: rat RH-35 whole cell lysates,
Lane 3: mouse lung tissue lysates,
Lane 4: mouse testis tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-MMP8 antigen affinity purified polyclonal antibody (BA2201) 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 MMP8 at approximately 53 kDa. The expected band size for MMP8 is at 53 kDa.
IHC analysis of MMP8 using anti-MMP8 antibody (BA2201) .
MMP8 was detected in a paraffin-embedded section of mouse spleen tissue. The tissue section was incubated with rabbit anti-MMP8 Antibody (BA2201) 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 MMP8 using anti-MMP8 antibody (BA2201) .
MMP8 was detected in a paraffin-embedded section of rat spleen tissue. The tissue section was incubated with rabbit anti-MMP8 Antibody (BA2201) 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 MMP8 using anti-MMP8 antibody (BA2201). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: rat PC-12 whole cell lysates,
Lane 2: rat RH-35 whole cell lysates,
Lane 3: mouse lung tissue lysates,
Lane 4: mouse testis tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-MMP8 antigen affinity purified polyclonal antibody (BA2201) 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 MMP8 at approximately 53 kDa. The expected band size for MMP8 is at 53 kDa.
IHC analysis of MMP8 using anti-MMP8 antibody (BA2201) .
MMP8 was detected in a paraffin-embedded section of mouse spleen tissue. The tissue section was incubated with rabbit anti-MMP8 Antibody (BA2201) 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 MMP8 using anti-MMP8 antibody (BA2201) .
MMP8 was detected in a paraffin-embedded section of rat spleen tissue. The tissue section was incubated with rabbit anti-MMP8 Antibody (BA2201) 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.