SLC19A2 Polyclonal / Unconjugated /
Product Details
| Description | Specificity of human, mouse, rat SLC19A2 antibody verified on a Protein Array containing target protein plus 383 other non-specific proteins. | |
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| Conjugate | Unconjugated | |
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| Target Species | Human | |
| Applications | IHC-P, IHC | |
| Supplier | Novus Biologicals | |
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About SLC19A2
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. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]
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. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]
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90 SLC19A2 antibodies from over 11 suppliers available with over 14 conjugates.
