Immobilized human GLUT1 VLP (Cat. No. CMP-24021) at 5 μg/mL (100 μL/well) can bind anti-human GLUT1 monoclonal antibody with EC50 range of 88.5-353.8 ng/mL (QC tested).
Bioactive, Human GLUT1 Full-Length Protein, Displayed on Nanoparticles
Glucose Transporter
Product Code: CMP-24021
Expression Host: HEK293T
Verified Applications: ELISA for GLUT1-specific antibody binding assays.
Human Glucose transporter 1 (GLUT1) is a 12-transmembrane protein that facilitates glucose transport. The recombinant GLUT1 full length protein (UniProt# P11166, amino acids Met1-Val492) is displayed on nanoparticles expressed in HEK293T cells (CMP-24021). The recombinant human GLUT1 protein binds GLUT1-specific antibodies. This GLUT1 protein mimics the native protein conformation on the cell surface and can be used as an antigen for in vitro assays and antibody screening.
Protein Name: GLUT1
UniProt #: P11166
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Protein Construct: The human GLUT1 full-length protein is displayed on nanoparticles and mimics the native protein conformation on the cell surface.
Background
Human Glucose transporter 1 (GLUT1) is a 12-transmembrane protein that facilitates glucose transport. GLUT1 is also known as solute carrier family 2, facilitated glucose transporter member 1 (SLC2A1). GLUT1 is a ubiquitously expressed glucose transporter responsible for basal glucose uptake. It plays a central role in cellular metabolism and is upregulated in response to hypoxia and metabolic stress to meet energetic and biosynthetic demands. GLUT1 mediates glucose transport by undergoing conformational shifts across the plasma membrane, allowing facilitated diffusion of glucose into cells. The GLUT1 crystal structure confirms a 12-transmembrane topology with both the N- and C- termini located intracellularly. GLUT1 is highly expressed in erythrocytes (red blood cells) and the blood-brain barrier (BBB) and present in placenta, kidneys, and endothelium of the central nerve system. GLUT1 is also a receptor used by human T-lymphotropic virus 1 (HTLV) to gain entry into target cells. GLUT1 is clinically significant due to its role in glucose transport, especially across the blood-brain barrier. GLUT1 gene mutation can result in several diseases. GLUT1 overexpression is also a hallmark of many cancers. Elevated GLUT1 enhances tumor glucose uptake, acidifies the tumor microenvironment, and contributes to immune evasion by outcompeting infiltrating T cells for glucose and impairing effector function. This makes GLUT1 a potential dual-action target—modulating tumor metabolism and immune response simultaneously.