FAM126A Antikörper

Produktnummer ABIN2856750

Dieser Anti-FAM126A Antikörper ist ein Kaninchen Polyklonal Antikörper zur Detektion von FAM126A in WB. Geeignet für Human.

Kurzübersicht für FAM126A Antikörper (ABIN2856750)

Target: FAM126A (Family with Sequence Similarity 126, Member A (FAM126A))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser FAM126A Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-FAM126A Antikörper

Kreuzreaktivität: Human, Maus

Produktmerkmale: Rabbit Polyclonal antibody to FAM126A (family with sequence similarity 126, member A)
FAM126A antibody [N3C3]

Aufreinigung: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein encompassing a sequence within the center region of human FAM126A. The exact sequence is proprietary.

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB: 1:1000-1:10000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Kommentare:

Positive Control: Raji , Mouse brain

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: 0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal

Konservierungsmittel: Thimerosal (Merthiolate)

Vorsichtsmaßnahmen: This product contains Thimerosal (Merthiolate): 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 FAM126A

Target: FAM126A (Family with Sequence Similarity 126, Member A (FAM126A))

Andere Bezeichnung: family with sequence similarity 126 member A

Hintergrund: The protein encoded by this gene may play a part in the beta-catenin/Lef signaling pathway. Expression of this gene is down-regulated by beta-catenin. Defects in this gene are a cause of hypomyelination with congenital cataract (HCC).

Cellular Localization: Cytoplasm , Membrane

Molekulargewicht: 58 kDa

Gen-ID: 84668

UniProt: Q9BYI3