PERK antibody

Untreated (–) and treated (+) NIH-3T3 whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with PERK antibody (GTX129275) diluted at 1:500. 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 (+) SK-N-SH whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with PERK antibody (GTX129275) diluted at 1:500. 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.

Whole cell extract (30 μg) was separated by 5% SDS-PAGE, and the membrane was blotted with PERK antibody (GTX129275) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

PERK antibody detects PERK protein at nucleus by immunohistochemical analysis.
Sample: Paraffin-embedded mouse brain.
PERK stained by PERK antibody (GTX129275) diluted at 1:500.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min

PERK antibody detects PERK protein at nucleus by immunohistochemical analysis.
Sample: Paraffin-embedded rat brain.
PERK stained by PERK antibody (GTX129275) diluted at 1:500.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min