SLC19A2 anticorps

N° du produit ABIN7468999

L’anticorps Lapin Polyclonal anti-SLC19A2 a été validé pour WB, ICC et IF. Il convient pour détecter SLC19A2 dans des échantillons de Humain.

Aperçu rapide pour SLC19A2 anticorps (ABIN7468999)

Antigène: SLC19A2 (Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SLC19A2 est non-conjugé

Application: Western Blotting (WB), Immunocytochemistry (ICC), Immunofluorescence (IF)

Détail du produit anti-SLC19A2 anticorps

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein encompassing a sequence within the center region of human SLC19A2. The exact sequence is proprietary.

Isotype: IgG

Information d'application

Indications d'application: WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Commentaires:

Positive Control: mouse liver

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1.3 mg/mL

Buffer: 1XPBS ( pH 7), 20 % Glycerol, 0.025 % ProClin 300

Agent conservateur: ProClin

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

Stock: 4 °C,-20 °C

Stockage commentaire: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Détails sur SLC19A2

Antigène: SLC19A2 (Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2))

Autre désignation: solute carrier family 19 member 2

Sujet:

Synonyms: solute carrier family 19 member 2 , TC1 , THMD1 , THT1 , THTR1 , TRMA

Background: This gene encodes the thiamin transporter protein. Mutations in this gene cause thiamin-responsive megaloblastic anemia syndrome (TRMA), which is an autosomal recessive disorder characterized by diabetes mellitus, megaloblastic anemia and sensorineural deafness. [provided by RefSeq]

Poids moléculaire: 55 kDa

ID gène: 10560

UniProt: O60779

Pathways: Dicarboxylic Acid Transport