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SLC19A2 Products

SLC19A2 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.
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8 results for "SLC19A2" in Products

8 results for "SLC19A2" in Products

SLC19A2 Products

SLC19A2 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.
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Applications: WB, ICC/IF
Reactivity: Human, Mouse, Rat
Applications: WB, ELISA
Reactivity: Human
Applications: WB, ELISA, MA, AP
Applications: WB
Reactivity: Human
Applications: WB
Reactivity: Human
Applications: WB
Applications: IHC
Reactivity: Human
Applications: AC
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