Glut5 Polyclonal Antibody, 20ul In vitro Assessment Mutations in this gene are

Mutations in this gene are associated with congenital hypothyroidism and cleft palate with thyroid dysgenesis

inter-well interference

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and a particular variation in HSD11B1 has been associated with obesity and insulin resistance in children

Glut5 Polyclonal Antibody, 20ul In vitro Assessment Mutations in this gene areSolute carrier family 2 facilitated glucose transporter member 5 encoded by SLC2A5 is a fructose transporter responsible for fructose uptake by the small intestine. The encoded protein also is necessary for the increase in blood pressure due to high dietary fructose consumption.