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Merck

SLC19A2

solute carrier family 19 (thiamine transporter), member 2

Sinónimos:
TC1, THMD1, THT1, THTR1, TRMA
Especie:
ID UniProtKB:
ID del gen:
  • Human(10560) Summary: 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]
  • Mouse(116914) solute carrier family 19 (thiamine transporter), member 2
  • Rat(289175) solute carrier family 19 (thiamine transporter), member 2
  • cow(532860) solute carrier family 19 (thiamine transporter), member 2
  • domestic cat(664737) solute carrier family 19 (thiamine transporter), member 2
  • Horse(100058457) solute carrier family 19 (thiamine transporter), member 2
  • dog(490353) solute carrier family 19 (thiamine transporter), member 2
  • chicken(427957) solute carrier family 19 (thiamine transporter), member 2
  • Zebrafish(569085) solute carrier family 19 (thiamine transporter), member 2
  • domestic guinea pig(100717365) solute carrier family 19 (thiamine transporter), member 2
  • naked mole-rat(101702163) solute carrier family 19 (thiamine transporter), member 2
  • sheep(101123393) solute carrier family 19 (thiamine transporter), member 2

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Antibodies

Referencia del producto
Descripción
Reactividad de especies
Aplicación
Anti-SLC19A2 antibody produced in rabbit, Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution,
Reactividad de especies
human
Aplicación
immunohistochemistry

esiRNA

Referencia del producto
Descripción
Especie
MISSION® esiRNA, targeting mouse Slc19a2,
Especie
mouse