Glucose transporters (GLUT) are integral membrane glycoproteins involved in transporting glucose into most cells. SLC2A1/GLUT1 facilitates glucose transport across the blood brain barrier. Functional defects of SLC2A1 cause autosomal dominant GLUT1 deficiency syndrome, which are characterized by infantile seizures, delayed development, hypoglucorrhachia, and acquired microcephaly.
Productname
Anti-SLC2A1 (GLUT1) (Human) pAb
BMP007
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
Anti-SLC2A1 (GLUT1) (Human) pAb
BMP007
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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