POLR3A antibody [HL3437]

Whole Japanese medaka extract (30 μg) was separated by 5% SDS-PAGE, and the membrane was blotted with POLR3A antibody [HL3437] (GTX641310) 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.

Whole zebrafish extract (30 μg) was separated by 5% SDS-PAGE, and the membrane was blotted with POLR3A antibody [HL3437] (GTX641310) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

POLR3A antibody [HL3437] detects POLR3A protein by immunofluorescent analysis.
Sample: HepG2 cells were fixed in ice-cold MeOH for 5 min.
Green: POLR3A stained by POLR3A antibody [HL3437] (GTX641310) diluted at 1:500.
Red: alpha Tubulin, a cytoskeleton marker, stained by alpha Tubulin antibody [GT114] (GTX628802) diluted at 1:1000.

POLR3A antibody [HL3437] detects POLR3A protein by immunohistochemical analysis.
Sample: Paraffin-embedded mouse tissues.
POLR3A stained by POLR3A antibody [HL3437] (GTX641310) diluted at 1:200.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min

POLR3A antibody [HL3437] detects POLR3A protein by immunohistochemical analysis.
Sample: Paraffin-embedded human tissues.
POLR3A stained by POLR3A antibody [HL3437] (GTX641310) diluted at 1:200.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min
Corresponding RNA levels (RPKM) in the tissues are based on NCBI database.

POLR3A antibody [HL3437] detects POLR3A protein by immunohistochemical analysis.
Sample: Paraffin-embedded rat tissues.
POLR3A stained by POLR3A antibody [HL3437] (GTX641310) diluted at 1:200.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min
Corresponding RNA levels (RPKM) in the tissues are based on NCBI database.

Various whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with POLR3A antibody [HL3437] (GTX641310) 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 5% SDS-PAGE, and the membrane was blotted with POLR3A antibody [HL3437] (GTX641310) diluted at 1:1000. 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.