NRF2抗体 [HL3183]

Immunoprecipitation of NRF2 protein from MG132 treated HepG2 whole cell extract using 5 μg of NRF2 antibody [HL3183] (GTX640822).
Western blot analysis was performed using NRF2 antibody [HL3183] (GTX640822).
EasyBlot HRP-conjugated anti anti Rabbit IgG (GTX221666-01), and the signal was developed with Trident femto Western HRP Substrate.

Untreated (–) and treated (+) HepG2 whole cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with NRF2 antibody [HL3183] (GTX640822) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Untreated (–) and treated (+) Rat2 whole cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with NRF2 antibody [HL3183] (GTX640822) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.

Untreated (–) and treated (+) Neuro2A whole cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with NRF2 antibody [HL3183] (GTX640822) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.