SLC19A2

gene product
THTR1, TRMA
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 antibodies from 19 providers.

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antibodies-online
27 antibodies
Invitrogen Antibodies
4 antibodies
Novus Biologicals
4 antibodies
Abnova Corporation
4 antibodies
Atlas Antibodies
2 antibodies
LifeSpan BioSciences, Inc.
17 antibodies
Abgent
1 antibody
GeneTex
1 antibody
NovoPro Bioscience Inc.
1 antibody
Biorbyt
10 antibodies
Aviva Systems Biology
1 antibody
OriGene
1 antibody
Bioss
3 antibodies
Boster Biological Technology
1 antibody
Creative Biolabs
4 antibodies
Sigma-Aldrich
3 antibodies
Creative Diagnostics
3 antibodies
MyBioSource
2 antibodies
Leading Biology
1 antibody