Rat tissue extract (50 μg) was separated by 10% SDS-PAGE, and the membrane was blotted with MAT1A + MAT2A antibody (GTX132095) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Mouse tissue extract (50 μg) was separated by 10% SDS-PAGE, and the membrane was blotted with MAT1A + MAT2A antibody (GTX132095) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Non-transfected (–) and transfected (+) 293T whole cell extracts (30 μg) were separated by 10% SDS-PAGE, and the membrane was blotted with MAT1A + MAT2A antibody (GTX132095) diluted at 1:5000. The HRP-conjugated anti-mouse IgG antibody (GTX213111-01) was used to detect the primary antibody, and the signal was developed with Trident femto Western HRP Substrate.

MAT1A + MAT2A antibody detects MAT1A + MAT2A protein at cytoplasm in mouse liver by immunohistochemical analysis.
Sample: Paraffin-embedded mouse liver.
MAT1A + MAT2A antibody (GTX132095) diluted at 1:500.

Antigen Retrieval: Citrate buffer, pH 6.0, 15 min

MAT1A + MAT2A antibody detects MAT1A + MAT2A protein at cytoplasm in rat liver by immunohistochemical analysis.
Sample: Paraffin-embedded rat liver.
MAT1A + MAT2A antibody (GTX132095) diluted at 1:500.

Antigen Retrieval: Citrate buffer, pH 6.0, 15 min