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. |
Figure 1. Western blot analysis of anti- SOD2 Antibody (M00349-3). The sample well of each lane was loaded with 50ug of sample under reducing conditions.
Lane 1: HEPG2 whole cell lysates,
Lane 2: HCCP tissue lysates,
Lane 3: HCCP tissue lysates,
Lane 4: mouse liver tissue lysates,
Lane 5: mouse heart tissue lysates.
Use mouse anti- SOD2 1:1000, probed with a goat anti-mouse IgG-HRP secondary antibody. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1001). A specific band was detected for SOD2 at approximately 25KD. The expected band size for SOD2 is at 25KD.
Figure 2. IHC analysis using anti- SOD2 Antibody (M00349-3). detected in paraffin-embedded section of human Adenocarcinoma of the right colon tissue. Peroxidase Conjugated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using HRP Conjugated mouse IgG Super Vision Assay Kit (Catalog#SV0001) with DAB as the chromogen.
Figure 3. IHC analysis using anti- SOD2 Antibody (M00349-3). detected in paraffin-embedded section of human liver cancer tissue. Peroxidase Conjugated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using HRP Conjugated mouse IgG Super Vision Assay Kit (Catalog#SV0001) with DAB as the chromogen.
Figure 4. IHC analysis using anti- SOD2 Antibody (M00349-3). detected in paraffin-embedded section of human lymphoma tissue. Peroxidase Conjugated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using HRP Conjugated mouse IgG Super Vision Assay Kit (Catalog#SV0001) with DAB as the chromogen.
Figure 1. Western blot analysis of anti- SOD2 Antibody (M00349-3). The sample well of each lane was loaded with 50ug of sample under reducing conditions.
Lane 1: HEPG2 whole cell lysates,
Lane 2: HCCP tissue lysates,
Lane 3: HCCP tissue lysates,
Lane 4: mouse liver tissue lysates,
Lane 5: mouse heart tissue lysates.
Use mouse anti- SOD2 1:1000, probed with a goat anti-mouse IgG-HRP secondary antibody. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1001). A specific band was detected for SOD2 at approximately 25KD. The expected band size for SOD2 is at 25KD.
Figure 2. IHC analysis using anti- SOD2 Antibody (M00349-3). detected in paraffin-embedded section of human Adenocarcinoma of the right colon tissue. Peroxidase Conjugated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using HRP Conjugated mouse IgG Super Vision Assay Kit (Catalog#SV0001) with DAB as the chromogen.
Figure 3. IHC analysis using anti- SOD2 Antibody (M00349-3). detected in paraffin-embedded section of human liver cancer tissue. Peroxidase Conjugated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using HRP Conjugated mouse IgG Super Vision Assay Kit (Catalog#SV0001) with DAB as the chromogen.
Figure 4. IHC analysis using anti- SOD2 Antibody (M00349-3). detected in paraffin-embedded section of human lymphoma tissue. Peroxidase Conjugated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using HRP Conjugated mouse IgG Super Vision Assay Kit (Catalog#SV0001) with DAB as the chromogen.