IRE1 alpha (phospho Ser724) antibody [HL4542]

Untreated (–) and treated (+) Neuro2A whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with IRE1 alpha (phospho Ser724) antibody [HL4542] (GTX644210) 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 femto Western HRP Substrate.

Untreated (–) and treated (+) Rat2 whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membranes were blotted with IRE1 alpha (phospho Ser724) antibody [HL4542] (GTX644210) diluted at 1:1000 and IRE1 alpha antibody (GTX113682) 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 femto Western HRP Substrate.

Untreated (–) and treated (+) HepG2 whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membranes were blotted with IRE1 alpha (phospho Ser724) antibody [HL4542] (GTX644210) diluted at 1:1000 and IRE1 alpha antibody (GTX113682) 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 5% SDS-PAGE, and the membranes were blotted with IRE1 alpha (phospho Ser724) antibody [HL4542] (GTX644210) diluted at 1:1000 and IRE1 alpha antibody (GTX113682) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.