GLUT1 Antibody for IF / SLC2A1 Glucose Transporter [clone CGG-19] (RQ5352)

GLUT1 Antibody for IF staining in human HepG2 cells. Fluorescent staining shows green signal corresponding to GLUT1 (SLC2A1) localization outlining the plasma membrane and cytoplasmic vesicular structures consistent with glucose transporter distribution in metabolically active cells. Membrane-associated fluorescence highlights cell boundaries while punctate cytoplasmic signal reflects intracellular transporter trafficking. Nuclei are counterstained with DAPI (blue). Signal was detected using an immunofluorescence method and visualized by fluorescence microscopy.

IHC staining of FFPE human cervical cancer with GLUT1 antibody. HIER: boil tissue sections in pH6, 10mM citrate buffer, for 10-20 min followed by cooling at RT for 20 min.

Flow cytometry testing of human HeLa cells with GLUT1 antibody; Red=cells alone, Blue= GLUT1 antibody.

Western blot testing of human HepG2 cell lysate with GLUT1 antibody. Predicted molecular weight ~55 kDa.

GLUT1 Antibody for IF staining in human HeLa cells. Immunofluorescence analysis using GLUT1 Antibody for IF at 1:50 dilution shows green fluorescent signal corresponding to GLUT1 (SLC2A1) localization along the plasma membrane and within cytoplasmic vesicular structures consistent with glucose transporter distribution in metabolically active cells. Phalloidin-TRITC (red) labels the actin cytoskeleton and outlines cell morphology, while DAPI (blue) marks cell nuclei. The merged image demonstrates membrane-associated GLUT1 fluorescence outlining individual cells and cytoplasmic transporter localization visualized by fluorescence microscopy.

GLUT1 Antibody immunohistochemistry analysis in human colon tissue. FFPE human colon section shows HRP-DAB brown membranous and cytoplasmic staining in epithelial cells lining the colonic glands, consistent with GLUT1 (SLC2A1) localization in metabolically active epithelial cell populations. Stromal cells and surrounding connective tissue show minimal background staining. The section was stained using GLUT1 antibody at 1:200 dilution.

GLUT1 Antibody immunohistochemistry analysis in human thymoma tissue. FFPE human thymoma section shows HRP-DAB brown membranous and cytoplasmic staining in tumor epithelial cells, consistent with GLUT1 (SLC2A1) localization in metabolically active tumor cell populations. Surrounding stromal components display minimal background staining. The section was stained using GLUT1 antibody at 1:200 dilution.

GLUT1 Antibody immunohistochemistry analysis in human stomach tissue. FFPE human stomach section shows HRP-DAB brown membranous and cytoplasmic staining in gastric epithelial cells lining glandular structures, consistent with GLUT1 (SLC2A1) localization in metabolically active epithelial cell populations. Surrounding stromal cells show minimal background staining. The section was stained using GLUT1 antibody at 1:800 dilution.

GLUT1 Antibody immunohistochemistry analysis in mouse kidney tissue. FFPE mouse kidney section shows HRP-DAB brown membranous and cytoplasmic staining in renal tubular epithelial cells, consistent with GLUT1 (SLC2A1) localization in metabolically active kidney cell populations. Glomerular structures and surrounding stromal regions show comparatively weaker staining. The section was stained using GLUT1 antibody at 1:300 dilution.

GLUT1 Antibody immunohistochemistry analysis in rat hippocampus tissue. FFPE rat hippocampus section shows HRP-DAB brown cytoplasmic and membranous staining in neuronal and neuropil regions consistent with GLUT1 (SLC2A1) localization in metabolically active brain tissue. The staining highlights cells within hippocampal layers while surrounding background remains minimal. The section was stained using GLUT1 antibody at 1:300 dilution.