WB
Western blot analysis of Cullin 4a on different lysates with Rabbit anti-Cullin 4a antibody at 1/2,000 dilution.
Lane 1: HeLa (Human cervical adenocarcinoma cell),
Lane 2: SK-MEL-28 (Human malignant melanoma cell),
Lane 3: AGS (Human stomach adenocarcinoma cell),
Lane 4: HT-29 (Human colorectal adenocarcinoma cell),
Lane 5: COS-7 (African green monkey kidney fibroblast),
Lysates/proteins at 10 µg/Lane.
Exposure time: 3 minutes;
Blocking: 5% NFDM/TBST, 1 hour at room temperature,
Primary antibody:1/2,000 in primary antibody dilution buffer, overnight at 4 ℃
Secondary antibody: Goat anti-Rabbit IgG-HR, 1/50,000 in 5% NFDM/TBST, 1 hour at room temperature
IHC
Immunohistochemical analysis of paraffin-embedded human breast cancer tissue with Rabbit anti-Cullin 4a antibody at 1/1,000 dilution.
The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
IHC
Immunohistochemical analysis of paraffin-embedded human kidney tissue with Rabbit anti-Cullin 4a antibody at 1/1,000 dilution.
The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
IHC
Immunohistochemical analysis of paraffin-embedded human testis tissue with Rabbit anti-Cullin 4a antibody at 1/1,000 dilution.
The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.