Whole zebrafish extract (30 μg) was separated by 15% SDS-PAGE, and the membrane was blotted with RPS26 antibody [HL3013] (GTX640426) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

RPS26 antibody [HL3013] detects RPS26 protein by immunofluorescent analysis.
Sample: HeLa cells were fixed in 4% paraformaldehyde at RT for 15 min.
Green: RPS26 stained by RPS26 antibody [HL3013] (GTX640426) diluted at 1:500.
Red: alpha Tubulin, a cytoskeleton marker, stained by alpha Tubulin antibody [GT114] (GTX628802) diluted at 1:1000.
Blue: Fluoroshield with DAPI (GTX30920).

RPS26 antibody [HL3013] detects RPS26 protein by immunohistochemical analysis.
Sample: Paraffin-embedded rat pancreas.
RPS26 stained by RPS26 antibody [HL3013] (GTX640426) diluted at 1:100.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min

Various whole cell extracts (30 μg) were separated by 15% SDS-PAGE, and the membrane was blotted with RPS26 antibody [HL3013] (GTX640426) 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 femto Western HRP Substrate.

Various whole cell extracts (30 μg) were separated by 15% SDS-PAGE, and the membrane was blotted with RPS26 antibody [HL3013] (GTX640426) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Various whole cell extracts (30 μg) were separated by 15% SDS-PAGE, and the membrane was blotted with RPS26 antibody [HL3013] (GTX640426) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.