Description
This gene encodes the thiamin transporter protein. Mutations in this gene cause thiamin-responsive megaloblastic anemia syndrome (TRMA), which is an autosomal recessive disorder characterized by diabetes mellitus, megaloblastic anemia and sensorineural deafness.

Specification
Aliases	TC1; THT1; TRMA; THMD1; THTR1
Swissprot	O60779
Host/Isotype	Rabbit IgG
Antibody Type	Primary antibody
Storage	Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Species Reactivity	Human
Immunogen	Fusion protein of human SLC19A2
Formulation	Purified antibody in PBS with 0.05% sodium azide and 50% glycerol.

Application
IHC	1/15-1/50
ELISA	1/1000-1/2000