Anti-Human SLC19A2 Polyclonal Antibody

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.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA12685
Size 100μl
Host Type Rabbit
Immunogen Recombinant protein of human SLC19A2
Specificity Ubiquitous; most abundant in skeletal and cardiac muscle. Medium expression in placenta, heart, liver and kidney, low in lung.
Isotype IgG
Reacitivity Human
Clone
Uniprot O60779
Concentration 0.1 mg/mL
Dilution IHC 1:15-1:50
Formulation
Application IHC,ELISA
Other Names S19A2,SLC19A2,Solute carrier family 19 member 2,TC1,Thiamine carrier 1,Thiamine transporter 1,THT1,ThTr 1,ThTr-1,ThTr1,TRMA
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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