ABCB6 Antikörper

Produktnummer ABIN2428945

Produktdetails anti-ABCB6 Antikörper

Target: ABCB6 (ATP-Binding Cassette, Sub-Family B (MDR/TAP), Member 6 (ABCB6))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ABCB6 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Aufreinigung: Affinity purification

Immunogen: Recombinant protein of human ABCB6

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:200-1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.1 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 ABCB6

Target: ABCB6 (ATP-Binding Cassette, Sub-Family B (MDR/TAP), Member 6 (ABCB6))

Andere Bezeichnung: ABCB6 (ABCB6 Produkte)

Synonyme: ABCB6 antikoerper, abcb6 antikoerper, ABC antikoerper, ABC14 antikoerper, LAN antikoerper, MCOPCB7 antikoerper, MTABC3 antikoerper, PRP antikoerper, umat antikoerper, 1200005B17Rik antikoerper, ATP binding cassette subfamily B member 6 (Langereis blood group) antikoerper, ATP binding cassette subfamily B member 6 antikoerper, ATP-binding cassette, sub-family B (MDR/TAP), member 6a antikoerper, ATP-binding cassette, sub-family B (MDR/TAP), member 6 antikoerper, ABCB6 antikoerper, abcb6a antikoerper, abcb6 antikoerper, Abcb6 antikoerper

Hintergrund: The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance as well as antigen presentation. This half-transporter likely plays a role in mitochondrial function. Localized to 2q26, this gene is considered a candidate gene for lethal neonatal metabolic syndrome, a disorder of mitochondrial function.

Molekulargewicht: Calculated MW: 94 kDa

Pathways: Transition Metal Ion Homeostasis