SLC11A2 Antikörper

Produktnummer ABIN2432955

Produktdetails anti-SLC11A2 Antikörper

Target: SLC11A2 (Solute Carrier Family 11 (Proton-Coupled Divalent Metal Ion Transporters), Member 2 (SLC11A2))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SLC11A2 Antikörper ist unkonjugiert

Applikation: ELISA, Immunohistochemistry (IHC)

Aufreinigung: Affinity purification

Immunogen: Synthetic peptide of human SLC11A2

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IHC 1:50-1:200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1.1 mg/mL

Buffer: PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

Konservierungsmittel: Sodium azide

Handhabung: Avoid freeze / thaw cycles.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu SLC11A2

Target: SLC11A2 (Solute Carrier Family 11 (Proton-Coupled Divalent Metal Ion Transporters), Member 2 (SLC11A2))

Andere Bezeichnung: SLC11A2 (SLC11A2 Produkte)

Synonyme: DCT1 antikoerper, DMT1 antikoerper, NRAMP2 antikoerper, Nramp2 antikoerper, mk antikoerper, van antikoerper, Dmt1 antikoerper, ATNRAMP2 antikoerper, F8G22.4 antikoerper, F8G22_4 antikoerper, NRAMP metal ion transporter 2 antikoerper, dct1 antikoerper, dmt1 antikoerper, nramp2 antikoerper, SLC11A2 antikoerper, cb426 antikoerper, fa07b10 antikoerper, wu:fa07b10 antikoerper, zgc:136699 antikoerper, solute carrier family 11 member 2 antikoerper, solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 antikoerper, NRAMP metal ion transporter 2 antikoerper, manganese transport protein antikoerper, metal transporter Nramp2 antikoerper, solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2 antikoerper, SLC11A2 antikoerper, Slc11a2 antikoerper, NRAMP2 antikoerper, LOC9327403 antikoerper, slc11a2 antikoerper

Hintergrund: 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.

NCBI Accession: NP_000608

Pathways: Transition Metal Ion Homeostasis, Proton Transport, Positive Regulation of Endopeptidase Activity