SLC19A2 产品
(Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2))
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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. [provided by RefSeq, Jul 2008].
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SLC19A2 抗体
High quality antibodies with extensive validation data.
Recommended SLC19A2 抗体
Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Application
ELISA, WB
Validations
- (4)
Cat. No.
ABIN523986
Quantity
100 μg
Datasheet
Datasheet
Reactivity
Human
Application
ELISA, IHC
Validations
- (2)
Cat. No.
ABIN7171980
Quantity
100 μg
Datasheet
Datasheet
Reactivity
Human
Application
WB
Validations
- (1)
Cat. No.
ABIN1327543
Quantity
50 μg
Datasheet
Datasheet
Recommended SLC19A2 蛋白
Synonyms and alternative names related to SLC19A2
solute carrier family 19 member 2 (Slc19a2), solute carrier family 19 member 2 (SLC19A2), solute carrier family 19 (thiamine transporter), member 2 (slc19a2), SLC19A2, TC1, THMD1, THT1, THTR1, TRMAProtein level used designations for SLC19A2
- thiamine transporter 1
- solute carrier family 19 (thiamine transporter), member 2
- Novel solute carrier family 19 protein
- thiamine transporter 1-like
- high affinity thiamine transporter
- reduced folate carrier protein (RFC) like
- solute carrier family 19 member 2
- thTr-1
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