Non-transfected (–) and transfected (+) HepG2 whole cell extracts (30 μg) were separated by 12% SDS-PAGE, and the membrane was blotted with GPX2 antibody [HL125] (GTX635477) diluted at 1:10000. The HRP-conjugated anti-mouse IgG antibody (GTX213111-01) was used to detect the primary antibody.

Various whole cell extracts (30 μg) were separated by 12% SDS-PAGE, and the membrane was blotted with GPX2 antibody [HL125] (GTX635477) diluted at 1:1000. The HRP-conjated 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.

GPX2 antibody [HL125] detects GPX2 protein at cytoplasm by immunohistochemical analysis.
Sample: Paraffin-embedded mouse colon.
GPX2 stained by GPX2 antibody [HL125] (GTX635477) diluted at 1:200.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min

Various tissue extracts (50 μg) were separated by 12% SDS-PAGE, and the membrane was blotted with GPX2 antibody [HL125] (GTX635477) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

GPX2 antibody [HL125] detects GPX2 protein at cytoplasm by immunohistochemical analysis.
Sample: Paraffin-embedded dog kidney.
GPX2 stained by GPX2 antibody [HL125] (GTX635477) diluted at 1:100.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min

GPX2 antibody [HL125] detects GPX2 protein by immunohistochemical analysis.
Sample: Paraffin-embedded rat tissues.
GPX2 stained by GPX2 antibody [HL125] (GTX635477) diluted at 1:100.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min

Whole zebrafish extract (30 μg) was separated by 12% SDS-PAGE, and the membrane was blotted with GPX2 antibody [HL125] (GTX635477) 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.