SLC40A1 anticorps

N° du produit ABIN701095

Cet anticorps Lapin Polyclonal détecte spécifiquement SLC40A1 dans WB, IHC (p) et IF (p). Il présente une réactivité avec des échantillons de Humain.

Aperçu rapide pour SLC40A1 anticorps (ABIN701095)

Antigène: SLC40A1 (Solute Carrier Family 40 (Iron-Regulated Transporter), Member 1 (SLC40A1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SLC40A1 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Détail du produit anti-SLC40A1 anticorps

Fonction: SLC40A1 Polyclonal Antibody

Réactivité croisée: Humain

Homologie: Mouse,Rat,Dog,Cow,Pig,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human SLC40A1

Isotype: IgG

Information d'application

Indications d'application: WB(1:300-5000), IHC-P(1:200-400), IF(IHC-P)(1:50-200)

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C for 12 months.

Date de péremption: 12 months

Détails sur SLC40A1

Antigène: SLC40A1 (Solute Carrier Family 40 (Iron-Regulated Transporter), Member 1 (SLC40A1))

Autre désignation: SLC40A1

Sujet:

Synonyms: Ferroportin 1, Ferroportin-1, FPN1, HFE4, IREG1, Iron regulated transporter 1, Iron-regulated transporter 1, MTP1, S40A1_HUMAN, SLC40A1, Solute carrier family 40 member 1, MST079, MSTP079, MTP1, SLC11A3.

Background: SLC40A1 may be involved in iron export from duodenal epithelial cells and also in transfer of iron between maternal and fetal circulation. It mediates iron efflux in the presence of a ferroxidase (hephaestin and/or ceruloplasmin). Defects in SLC40A1 are the cause of hemochromatosis type 4, an autosomal dominant iron-loading disorder characterized by early iron accumulation in reticuloendothelial cells and a marked increase in serum ferritin.

Poids moléculaire: 63kDa

ID gène: 30061

Pathways: Transition Metal Ion Homeostasis