Background：This gene encodes a major glucose transporter in the mammalian blood-brain barrier. Mutations in this gene have been found in a family with paroxysmal exertion-induced dyskinesia. Facilitative glucose transporter. This isoform may be responsible for constitutive or basal glucose uptake. Has a very broad substrate specificity; can transport a wide range of aldoses including both pentoses and hexoses.
仕様
Synonyms：Choreoathetosis/spasticity episodic （paroxysmal choreoathetosis/spasticity）,CSE,DYT17,DYT18,DYT9,EIG12,erythrocyte/brain,Erythrocyte/hepatoma glucose transporter,facilitated glucose transporter member 1,Glucose transporter 1,Glucose transporter type 1,Glucose transporter type 1,erythrocyte/brain,GLUT,GLUT-1,GLUT1,GLUT1DS,GLUTB,GT1,GTG1,Gtg3,GTR1,HepG2 glucose transporter,HTLVR,Human T cell leukemia virus （I and II） receptor,MGC141895,MGC141896,PED,RATGTG1,Receptor for HTLV 1 and HTLV 2,SLC2A1,Solute carrier family 2 （facilitated glucose transporter）,member 1,Solute carrier family 2,Solute carrier family 2,facilitated glucose transporter member 1
Host：Rabbit
Reactivity：Human,Mouse,Rat
Applications：WB,IHC,ELISA
Concentration：0.4mg/mL
Immunogen：Synthetic peptide of human SLC2A1
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：PBS with 0.05％ sodium azide, 50％ glycerol, PH7.3
Dilution：WB 1：500-1：2000, IHC 1：50-1：200
Swissprot：P11166
Isotype：IgG
Research Areas：Cancer, Cardiovascular, Metabolism, Signal transduction
