兔抗SLC19A2多克隆抗体

Background:

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.

Applications:

ELISA, IHC

Name of antibody:

SLC19A2

Immunogen:

Fusion protein of human SLC19A2

Full name:

solute carrier family 19 (thiamine transporter), member 2

Synonyms：

TC1; THT1; TRMA; THMD1; THTR1

SwissProt:

O60779

ELISA Recommended dilution:

1000-2000

IHC positive control:

Human brain

IHC Recommend dilution:

15-50