Various whole cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with GLUD1+ GLUD2 antibody [HL2124] (GTX638096) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody. Corresponding RNA expression data for the same cell lines are based on Human Protein Atlas program.

GLUD1+ GLUD2 antibody [HL2124] detects GLUD1+ GLUD2 protein by immunohistochemical analysis.
Sample: Paraffin-embedded rat liver.
GLUD1+ GLUD2 stained by GLUD1+ GLUD2 antibody [HL2124] (GTX638096) diluted at 1:100.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min

GLUD1+ GLUD2 antibody [HL2124] detects GLUD1+ GLUD2 protein at mitochondria by immunohistochemical analysis.
Sample: Paraffin-embedded mouse duodenum.
GLUD1+ GLUD2 stained by GLUD1+ GLUD2 antibody [HL2124] (GTX638096) diluted at 1:100.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min

Non-transfected (–) and transfected (+) 293T whole cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with GLUD1+GLUD2 antibody [HL2124] (GTX638096) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Various tissue extracts (50 μg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with GLUD1+GLUD2 antibody [HL2124] (GTX638096) diluted at 1:10000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.