|Immunohistochemistry (Paraffin) (IHC (P))||15 - 20 µg/ml|
|Tested Species reactivity||Human|
|Host / Isotype||Rabbit / IgG|
|Immunogen||Synthetic 16 amino acid peptide from internal region of human SLC11A2.|
|Purification||Antigen affinity chromatography|
|Contains||< 0.1% sodium azide|
|Storage conditions||Maintain refrigerated at 2-8°C for up to 1 month. For long term storage store at -20°C|
Percent identity with other species by BLAST analysis: Human, Chimpanzee, Gorilla, Orangutan, Gibbon, Monkey, Marmoset (100%) Galago, Rat, Hamster, Bovine, Horse (94%).
This gene encodes a member of the solute carrier family 11 protein family. The product of this gene transports divalent metals and is involved in iron absorption. Mutations in this gene are associated with hypochromic microcytic anemia with iron overload. A related solute carrier family 11 protein gene is located on chromosome 2. Multiple transcript variants encoding different isoforms have been found for this gene.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Dct-1; DCT1; Divalent cation transporter 1; Divalent metal transporter 1; DMT-1; DMT1; Natural resistance-associated macrophage protein 2; NRAMP 2; NRAMP2; SLC11A2; solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2; solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2; Solute carrier family 11 member 2
Gene Aliases: AHMIO1; DCT1; DMT1; NRAMP2; OK/SW-cl.20; SLC11A2
UniProt ID: (Human) P49281
Entrez Gene ID: (Human) 4891
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