-
Western blot analysis of Cathepsin L on different lysates with Rabbit anti-Cathepsin L antibody (HA722064) at 1/5,000 dilution.
Lane 1: A549 cell lysate (15 µg/Lane)
Lane 2: HepG2 cell lysate (15 µg/Lane)
Lane 3: HEK-293 cell lysate (15 µg/Lane)
Lane 4: MDA-MB-231 cell lysate (15 µg/Lane)
Lane 5: Human kidney tissue lysate (30 µg/Lane)
Lane 6: Human liver tissue lysate (30 µg/Lane)
Lane 7: NIH/3T3 cell lysate (15 µg/Lane)
Lane 8: PC-12 cell lysate (15 µg/Lane)
Lane 9: Mouse kidney tissue lysate (30 µg/Lane)
Lane 10: Rat kidney tissue lysate (30 µg/Lane)
Lane 11: Mouse liver tissue lysate (30 µg/Lane)
Lane 12: Rat liver tissue lysate (30 µg/Lane)
Lane 13: COS-1 cell lysate (15 µg/Lane)
Predicted band size: 38 kDa
Observed band size: 20-45 kDa
Exposure time: 10 seconds;
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 (HA722064) at 1/5,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.
-
Immunohistochemical analysis of paraffin-embedded human kidney tissue with Rabbit anti-Cathepsin L antibody (HA722064) at 1/10,000 dilution.
The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 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 (HA722064) 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.
-
Immunohistochemical analysis of paraffin-embedded mouse kidney tissue with Rabbit anti-Cathepsin L antibody (HA722064) at 1/10,000 dilution.
The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 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 (HA722064) 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.
-
Immunohistochemical analysis of paraffin-embedded rat kidney tissue with Rabbit anti-Cathepsin L antibody (HA722064) at 1/10,000 dilution.
The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 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 (HA722064) 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.
-
☑ Knockdown (KD)
Western blot analysis of Cathepsin L on different lysates with Rabbit anti-Cathepsin L antibody (HA722064) at 1/5,000 dilution.
Lane 1: HCT 116-si NT cell lysate (10 µg/Lane)
Lane 2: HCT 116-si Cathepsin L cell lysate (10 µg/Lane)
Predicted band size: 38 kDa
Observed band size: 20 kDa
Exposure time: 10 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 (HA722064) at 1/5,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"