Glucose transporter 1 (Glut-1) also known as solute carrier family 2, facilitated glucose transporter member 1 (SLC2A1), is a uniporter protein. GLUT1 expression is correlated with FDG uptake by Extrahepatic bile duct (EHD) cancers. GLUT-1-deficiency syndrome is a treatable metabolic disorder caused by a mutation of mutation of SLC2A1 gene. The functional deficiency of the GLUT1 protein leads to an impaired glucose transport into the brain, resulting in neurologic disorders gene.
Productname
Monoclonal Antibody to Glut-1 (Clone: ABM4G40)
10-7548
By filling out this form, you are placing an order by e-mail. You will receive an order confirmation within one working day. The order cannot be modified after receipt of the order confirmation.
Productname
Monoclonal Antibody to Glut-1 (Clone: ABM4G40)
10-7548
By filling out this form, you request a sample. You will receive an order confirmation within one working day. The order cannot be modified after receipt of the order confirmation.
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