SLC2A13 Polyclonal Antibody

Reddot Biotech

SLC2A13 Polyclonal Antibody

5

ImmunoHistoChemistry

Research Use Only

1 mg/ml

Unconjugated

SLC2A13

solute carrier family 2 member 13

h(+)-myo-inositol cotransporter; H(+)-myo-inositol symporter; HMIT; proton (H+) myo-inositol symporter; proton myo-inositol cotransporter; solute carrier family 2 (facilitated glucose transporter), member 13

Rabbit

IgG

SLC2A13 (Solute Carrier Family 2 Member 13) is a Protein Coding gene. Diseases associated with SLC2A13 include Arterial Tortuosity Syndrome. Among its related pathways are NRF2 pathway and Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds. Gene Ontology (GO) annotations related to this gene include carbohydrate:proton symporter activity. An important paralog of this gene is SLC2A2.

Human, Mouse, Rat

-20°C

12352203