Search Thermo Fisher Scientific
- Order Status
- Quick Order
-
Don't have an account ? Create Account
Search Thermo Fisher Scientific
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.
AHMIO1; DCT1; Dct-1; Divalent cation transporter 1; divalent metal transporter 1; DMT1; DMT-1; microcytic anemia, viable anaemia; mk; Natural resistance-associated macrophage protein 2; NRAMP 2; Nramp2; OK/SW-cl.20; 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; Solute carrier family 11 member 2 (natural resistance-associated macrophage protein 2); van
400 µL
50 µg
100 µL
50 µg
100 µL
100 µg
100 µg
100 µg
100 µg
100 µL
100 µL
100 µL
100 µg
100 µg
100 µL
Searching for an antibody we don't offer? We make custom antibodies for specific targets, species and applications.
More than 18,000 custom antibodies created so far.
Talk to a specialist nowIf an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*
Learn moreGet expert recommendations for common problems or connect directly with an on staff expert for technical assistance related to applications, equipment and general product use.
Contact tech support