SLC19A2 Antibody (Center) Blocking Peptide
€363.00
In stock
SKU
AC-BP16928c
Background:
This gene encodes the thiamin transporter protein.Mutations in this gene cause thiamin-responsive megaloblasticanemia syndrome (TRMA), which is an autosomal recessive disordercharacterized by diabetes mellitus, megaloblastic anemia andsensorineural deafness.
Other Names:
Thiamine transporter 1, ThTr-1, ThTr1, Solute carrier family 19 member 2, Thiamine carrier 1, TC1, SLC19A2, THT1, TRMA
Gene Name: SLC19A2
Gene ID: 10560
Primary Accession: O60779
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
This gene encodes the thiamin transporter protein.Mutations in this gene cause thiamin-responsive megaloblasticanemia syndrome (TRMA), which is an autosomal recessive disordercharacterized by diabetes mellitus, megaloblastic anemia andsensorineural deafness.
Other Names:
Thiamine transporter 1, ThTr-1, ThTr1, Solute carrier family 19 member 2, Thiamine carrier 1, TC1, SLC19A2, THT1, TRMA
Gene Name: SLC19A2
Gene ID: 10560
Primary Accession: O60779
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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