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Western blot analysis of p16INK4a on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (ET1608-62, 1/1,000) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.
Positive control:
Lane 1: 293 cell lysate
Lane 2: SiHa cell lysate
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☑ Knockdown (KD)
Western blot analysis of p16INK4a on different lysates with Rabbit anti-p16INK4a antibody (ET1608-62) at 1/1,000 dilution.
Lane 1: HeLa-si NT cell lysate
Lane 2: HeLa-si p16INK4a cell lysate
Lysates/proteins at 15 µg/Lane.
Predicted band size: 16 kDa
Observed band size: 16 kDa
Exposure time: 20 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 (ET1608-62) at 1/1,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/100,000 dilution was used for 1 hour at room temperature.
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