SLC2A5 Antibody / Sugar Transport Protein Antibody (R32418)

SLC2A5 Antibody Rat Brain and K562 WB. Western blot analysis of SLC2A5 expression using an SLC2A5 antibody. Lane 1: rat brain lysate. Lane 2: human K562 cell lysate. SLC2A5, also known as GLUT5 and Sugar Transport Protein, is a facilitative transporter that preferentially mediates fructose uptake and contributes to cellular energy metabolism. A prominent band is detected at approximately 55 kDa in both samples, consistent with the expected molecular weight of SLC2A5. These results demonstrate endogenous expression of this nutrient transporter in rodent and human tissues and support the utility of SLC2A5 Antibody for studies of fructose transport, carbohydrate metabolism, and metabolic regulation.

SLC2A5 Antibody Intestinal Cancer IHC. Immunohistochemical staining of FFPE human intestinal cancer tissue demonstrates SLC2A5 expression using an SLC2A5 antibody. SLC2A5, also known as GLUT5 and Sugar Transport Protein, is a facilitative transporter that mediates fructose uptake and contributes to cellular energy metabolism. Prominent membranous and cytoplasmic staining is observed in malignant epithelial cells, consistent with the increased nutrient requirements and metabolic reprogramming associated with cancer. Heat induced epitope retrieval was performed by boiling tissue sections in pH 6 10 mM citrate buffer for 20 minutes followed by cooling prior to staining. These results support the utility of SLC2A5 Antibody for studies of fructose transport, cancer metabolism, and nutrient homeostasis.

SLC2A5 Antibody Rat Intestine IHC. Immunohistochemical staining of FFPE rat intestine demonstrates SLC2A5 expression using an SLC2A5 antibody. SLC2A5, also known as GLUT5 and Sugar Transport Protein, is a facilitative transporter that preferentially mediates fructose uptake and plays a central role in intestinal carbohydrate absorption. Predominantly apical and cytoplasmic staining is observed in intestinal epithelial cells, consistent with the localization of GLUT5 in enterocytes responsible for dietary fructose transport. Heat induced epitope retrieval was performed by boiling tissue sections in pH 6 10 mM citrate buffer for 20 minutes followed by cooling prior to staining. These results support the utility of SLC2A5 Antibody for studies of fructose transport, nutrient absorption, and metabolic regulation.