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☑ Knockdown (KD)
Western blot analysis of CYFIP1 on different lysates with Rabbit anti-CYFIP1 antibody (HA721095) at 1/1,000 dilution.
Lane 1: HAP1-parental cell lysate
Lane 2: HAP1-CYFIP1 KD cell lysate
Lysates/proteins at 10 µg/Lane.
Predicted band size: 145 kDa
Observed band size: 130 kDa
Exposure time: 180 seconds; ECL: K1801;
4-20% SDS-PAGE gel.
Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA721095) at 1/1,000 dilution was used in K1803 at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.
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Western blot analysis of CYFIP1 on different lysates with Rabbit anti-CYFIP1 antibody (HA721095) at 1/1,000 dilution.
Lane 1: SW480 (Human colorectal zdenocarcinoma cell) cell lysate
Lane 2: NIH/3T3 (Mouse fibroblast) cell lysate
Lysates/proteins at 10 µg/Lane.
Exposure time: 150 seconds; ECL: K1802
Blocking: 5% NFDM/TBST, 1 hour at room temperature
Primary antibody: HA721095, 1/1,000 in 5% NFDM/TBST, overnight at 4 ℃
Secondary antibody: Goat anti-Rabbit IgG-HRP (HA1001), 1/50,000 in 5% NFDM/TBST, 1 hour at room temperature
Predicted band size: 145.2 kDa
Observed band size: 130 kDa
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Western blot analysis of CYFIP1 on rat lung tissue lysates with Rabbit anti-CYFIP1 antibody (HA721095) at 1/500 dilution.
Lysates/proteins at 20 µg/Lane.
Predicted band size: 145 kDa
Observed band size: 130 kDa
Exposure time: 30 minutes;
6% SDS-PAGE gel.
Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA721095) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:300,000 dilution was used for 1 hour at room temperature.
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Immunohistochemical analysis of paraffin-embedded rat esophagus tissue with Rabbit anti-CYFIP1 antibody (HA721095) at 1/100 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 (HA721095) at 1/100 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.
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Immunohistochemical analysis of paraffin-embedded rat stomach tissue with Rabbit anti-CYFIP1 antibody (HA721095) at 1/400 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 (HA721095) at 1/400 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.
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