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
Reactivity: | Human, Mouse, Rat |
Details: | Rabbit IgG Polyclonal |
Applications: | WB, ICC/IF |
Reactivity: | Human |
Details: | Mouse IgG2a Kappa Monoclonal Clone #5B10 |
Applications: | WB, ELISA |
Applications: | WB, ELISA, MA, AP |
Reactivity: | Human |
Details: | Rabbit Polyclonal |
Applications: | WB |
Reactivity: | Human |
Details: | Mouse IgG Polyclonal |
Applications: | WB |
Applications: | WB |
Reactivity: | Human |
Details: | Rabbit IgG Polyclonal |
Applications: | IHC |
Applications: | AC |