SLC19A2 Antikörper

Produktnummer ABIN7468999

Der Kaninchen Polyklonal Anti-SLC19A2-Antikörper wurde für WB, ICC und IF validiert. Er ist geeignet, SLC19A2 in Proben von Human zu detektieren.

Kurzübersicht für SLC19A2 Antikörper (ABIN7468999)

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

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SLC19A2 Antikörper ist unkonjugiert

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

Produktdetails anti-SLC19A2 Antikörper

Kreuzreaktivität: Human, Maus, Ratte

Aufreinigung: Purified by antigen-affinity chromatography.

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

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: 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.

Kommentare:

Positive Control: mouse liver

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1.3 mg/mL

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

Konservierungsmittel: ProClin

Vorsichtsmaßnahmen: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: 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.

Details zu SLC19A2

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

Andere Bezeichnung: solute carrier family 19 member 2

Hintergrund:

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]

Molekulargewicht: 55 kDa

Gen-ID: 10560

UniProt: O60779

Pathways: Dicarboxylic Acid Transport