Various whole cell extracts (30 μg) were separated by 10% SDS-PAGE, and the membrane was blotted with OAT antibody [HL2087] (GTX637995) 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. Corresponding RNA expression data for the same cell lines are based on Human Protein Atlas program.

Non-transfected (–) and transfected (+) 293T whole cell extracts (30 μg) were separated by 10% SDS-PAGE, and the membrane was blotted with OAT antibody [HL2087] (GTX637995) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

OAT antibody [HL2087] detects OAT protein at mitochondria by immunofluorescent analysis.
Sample: A431 cells were fixed in ice-cold MeOH for 5 min.
Green: OAT stained by OAT antibody [HL2087] (GTX637995) diluted at 1:500.
Blue: Fluoroshield with DAPI (GTX30920).
Scale bar= 10μm.

OAT antibody [HL2087] detects OAT protein at cytoplasm by immunohistochemical analysis.
Sample: Paraffin-embedded rat stomach.
OAT stained by OAT antibody [HL2087] (GTX637995) diluted at 1:100.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min

OAT antibody [HL2087] detects OAT protein at cytoplasm by immunohistochemical analysis.
Sample: Paraffin-embedded mouse adrenal gland.
OAT stained by OAT antibody [HL2087] (GTX637995) diluted at 1:100.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min