Background：This gene encodes a nucleoside transporter. The encoded protein plays a role in cellular uptake of nucleosides, nucleobases, and their related analogs. Mutations in this gene have been associated with H syndrome, which is characterized by cutaneous hyperpigmentation and hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism. A related disorder, PHID （pigmented hypertrichosis with insulin-dependent diabetes mellitus）, has also been associated with mutations at this locus. Alternatively spliced transcript variants have been described.
仕様
Synonyms：ENT3,Equilibrative nucleoside transporter 3,HCLAP,hENT3,HJCD,PHID,S29A3,SLC29A3,Solute carrier family 29 （equilibrative nucleoside transporter） member 3,Solute carrier family 29 （nucleoside transporters） member 3,Solute carrier family 29 member 3
Host：Rabbit
Reactivity：Human
Applications：WB
Concentration：1mg/ml
Immunogen：Recombinant protein of human SLC29A3
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：Buffer： PBS with 0.02％ sodium azide, 50％ glycerol, pH7.3.
