SLC19A2 Antikörper (AA 21-120) (Biotin)

Produktnummer ABIN6944892

Produktdetails anti-SLC19A2 Antikörper (Biotin)

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

Bindungsspezifität: AA 21-120

Reaktivität: Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SLC19A2 Antikörper ist konjugiert mit Biotin

Applikation: ELISA, Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Spezifität: Possible cross-reactivity with SLC19A3 in human samples

Kreuzreaktivität: Maus

Homologie: Human,Rat,Dog,Cow,Pig,Horse,Rabbit

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human SLC19A2

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Konservierungsmittel: ProClin

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C for 12 months.

Haltbarkeit: 12 months

Details zu SLC19A2

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

Andere Bezeichnung: SLC19A2 (SLC19A2 Produkte)

Synonyme: SLC19A2 antikoerper, TC1 antikoerper, THMD1 antikoerper, THT1 antikoerper, THTR1 antikoerper, TRMA antikoerper, solute carrier family 19 member 2 antikoerper, solute carrier family 19 (thiamine transporter), member 2 antikoerper, Slc19a2 antikoerper, SLC19A2 antikoerper, slc19a2 antikoerper

Hintergrund:

Synonyms: Thiamine transporter 1, S19A2_HUMAN, SLC19A2, Solute carrier family 19 member 2, TC1, Thiamine carrier 1, THT1, ThTr 1, ThTr-1, 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, Jul 2008]

Gen-ID: 10560

UniProt: O60779

Pathways: Dicarboxylic Acid Transport