FOXA1 antibody [HL3168]

Non-transfected (–) and transfected (+) HepG2 whole cell extracts (30 μg) were separated by 10% SDS-PAGE, and the membrane was blotted with FOXA1 antibody [HL3168] (GTX640686) diluted at 1:2000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

FOXA1 antibody [HL3168] detects FOXA1 protein by immunohistochemical analysis.
Sample: Paraffin-embedded 1 day-post-fertilization zebrafish embryo.
Green: FOXA1 stained by FOXA1 antibody [HL3168] (GTX640686) diluted at 1:250.
Antigen Retrieval: Tris-HCl buffer, pH 9.0, 20 min at 70ºC

FOXA1 antibody [HL3168] detects FOXA1 protein by immunohistochemical analysis.
Sample: Paraformaldehyde-fixed 1 day-post-fertilization zebrafish embryo.
Green: FOXA1 stained by FOXA1 antibody [HL3168] (GTX640686) diluted at 1:250.
Antigen Retrieval: Tris-HCl buffer, pH 9.0, 20 min at 70ºC

Whole zebrafish extract (30 μg) was separated by 10% SDS-PAGE, and the membrane was blotted with FOXA1 antibody [HL3168] (GTX640686) 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.

FOXA1 antibody [HL3168] detects FOXA1 protein by immunohistochemical analysis.
Sample: Paraffin-embedded mouse stomach.
FOXA1 stained by FOXA1 antibody [HL3168] (GTX640686) diluted at 1:100.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min

FOXA1 antibody [HL3168] detects FOXA1 protein by immunofluorescent analysis.
Sample: MCF-7 cells were fixed in 4% paraformaldehyde at RT for 15 min.
Green: FOXA1 stained by FOXA1 antibody [HL3168] (GTX640686) diluted at 1:500.
Red: alpha Tubulin, a cytoskeleton marker, stained by alpha Tubulin antibody [GT114] (GTX628802) diluted at 1:1000.

Various whole cell extracts (30 μg) were separated by 10% SDS-PAGE, and the membrane was blotted with FOXA1 antibody [HL3168] (GTX640686) 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.

Various tissue extracts (50 μg) were separated by 10% SDS-PAGE, and the membrane was blotted with FOXA1 antibody [HL3168] (GTX640686) 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.