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Western blot analysis of MALT1 on different lysates with Rabbit anti-MALT1 antibody (HA750563) at 1/5,000 dilution and competitor's antibody at 1/1,000 dilution.
Lane 1: HCT 116 cell lysate (15 µg/Lane)
Lane 2: HeLa cell lysate (15 µg/Lane)
Lane 3: Ramos cell lysate (15 µg/Lane)
Lane 4: Daudi cell lysate (15 µg/Lane)
Lane 5: K-562 cell lysate (15 µg/Lane)
Lane 6: Mouse thymus tissue lysate (30 µg/Lane)
Lane 7: Rat thymus tissue lysate (30 µg/Lane)
Predicted band size: 92 kDa
Observed band size: 92 kDa
Exposure time: 2 minutes 6 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 (HA750563) at 1/5,000 dilution and competitor's antibody at 1/1,000 dilution were 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.
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Immunohistochemical analysis of paraffin-embedded human colon tissue with Rabbit anti-MALT1 antibody (HA750563) at 1/200 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 (HA750563) at 1/200 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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Western blot analysis of MALT1 on different lysates with Rabbit anti-MALT1 antibody (HA750563) at 1/1,000 dilution.
Lane 1: HCT 116 cell lysate (20 µg/Lane)
Lane 2: HeLa cell lysate (20 µg/Lane)
Lane 3: Ramos cell lysate (20 µg/Lane)
Lane 4: K-562 cell lysate (20 µg/Lane)
Lane 5: Jurkat cell lysate (20 µg/Lane)
Lane 6: HepG2 cell lysate (20 µg/Lane)
Lane 7: 786-0 cell lysate (20 µg/Lane)
Lane 8: LNCaP cell lysate (20 µg/Lane)
Lane 9: PC-3M cell lysate (20 µg/Lane)
Lane 10: Mouse lymph node tissue lysate (no heat) (40 µg/Lane)
Lane 11: Mouse thymus tissue lysate (40 µg/Lane)
Lane 12: Rat thymus tissue lysate (40 µg/Lane)
Notice: no heat means the lysate is not boiled.
Predicted band size: 92 kDa
Observed band size: 92 kDa
Exposure time: 37 seconds; ECL: K1802;
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 (HA750563) at 1/1,000 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.
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Immunohistochemical analysis of paraffin-embedded human colon cancer tissue with Rabbit anti-MALT1 antibody (HA750563) at 1/200 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 (HA750563) at 1/200 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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☑ Knockdown (KD)
Western blot analysis of MALT1 on different lysates with Rabbit anti-MALT1 antibody (HA750563) at 1/5,000 dilution.
Lane 1: HeLa-si NT cell lysate
Lane 2: HeLa-si MALT1 cell lysate
Lysates/proteins at 10 µg/Lane.
Predicted band size: 92 kDa
Observed band size: 92 kDa
Exposure time: 11 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 (HA750563) 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.
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