Glut1 Polyclonal Antibody, 50ul Cell Culture Plates Mutations in this gene are

Mutations in this gene are associated with erythrocytosis familial type 4

and phopholipase D activation

AMPD2 and AMPD3

Ras GTPase-activating protein 3 functions as a negative regulator of the Ras signalling pathway

which has a high affinity for both sulfated and nonsulfated CCK analogs and is found principally in the central nervous system and the gastrointestinal tract

Glut1 Polyclonal Antibody, 50ul Cell Culture Plates Mutations in this gene areSLC2A1 encodes a major glucose transporter in the mammalian blood brain barrier. Solute carrier family 2 facilitated glucose transporter member 1 is found primarily in the cell membrane and on the cell surface, where it can also function as a receptor for human T cell leukemia virus (HTLV) I and II. Mutations in this gene have been found in a family with paroxysmal exertion induced dyskinesia.