GLUT1 polyclonal, anti-human, mouse, rat
€469.00
In stock
SKU
252214
Protein Family: Transporters
Pathway and Disease: Cancers, Carbohydrate Metabolism, Development and Behavior, Endocrine System, Membrane Transport, Metabolic Disorders
Description:
Glucose transporter type 1 (GLUT1 or SLC2A1) is a glucose transporter responsible for constitutive or basal glucose uptake. GLUT1 has a very broad substrate specificity such as pentoses and hexoses. GLUT1 is expressed at variable levels in many human tissues. Defects in GLUT1 are the cause of autosomal dominant GLUT1 deficiency syndrome, a blood-brain barrier glucose transport defect characterized by infantile seizures and delayed development. Defects in GLUT1 are also the cause of dystonia type 18 (DYT18), an exercise-induced paroxysmal dystonia/dyskinesia (muscle contraction disorders).
Alternate Names: GLUT1, Glucose transporter type 1, GLUT-1, Solute carrier family 2, facilitated glucose transporter member 1, HepG2 glucose transporter, SLC2A1
Application Notes: E: 1:1,000-1:10,000; WB: 2:100-1:500
Accession No.: P11166
Antigen: KLH-conjugated synthetic peptide encompassing a sequence within the N-term region of human GLUT1.
Format: Each vial contains 0.1 mg IgG in 0.1 ml (1 mg/ml) of PBS pH7.4 with 0.09% sodium azide. Antibody was purified by Protein-G affinity chromatography.
Storage:
Store at -20°C. Minimize freeze-thaw cycles. Product is guaranteed one year from the date of shipment.
Pathway and Disease: Cancers, Carbohydrate Metabolism, Development and Behavior, Endocrine System, Membrane Transport, Metabolic Disorders
Description:
Glucose transporter type 1 (GLUT1 or SLC2A1) is a glucose transporter responsible for constitutive or basal glucose uptake. GLUT1 has a very broad substrate specificity such as pentoses and hexoses. GLUT1 is expressed at variable levels in many human tissues. Defects in GLUT1 are the cause of autosomal dominant GLUT1 deficiency syndrome, a blood-brain barrier glucose transport defect characterized by infantile seizures and delayed development. Defects in GLUT1 are also the cause of dystonia type 18 (DYT18), an exercise-induced paroxysmal dystonia/dyskinesia (muscle contraction disorders).
Alternate Names: GLUT1, Glucose transporter type 1, GLUT-1, Solute carrier family 2, facilitated glucose transporter member 1, HepG2 glucose transporter, SLC2A1
Application Notes: E: 1:1,000-1:10,000; WB: 2:100-1:500
Accession No.: P11166
Antigen: KLH-conjugated synthetic peptide encompassing a sequence within the N-term region of human GLUT1.
Format: Each vial contains 0.1 mg IgG in 0.1 ml (1 mg/ml) of PBS pH7.4 with 0.09% sodium azide. Antibody was purified by Protein-G affinity chromatography.
Storage:
Store at -20°C. Minimize freeze-thaw cycles. Product is guaranteed one year from the date of shipment.
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