EIF4H Antikörper

Produktnummer ABIN7467331

Der Kaninchen Polyklonal Anti-EIF4H-Antikörper wurde für WB, IF und ICC validiert. Er ist geeignet, EIF4H in Proben von Human zu detektieren.

Kurzübersicht für EIF4H Antikörper (ABIN7467331)

Target: EIF4H (Eukaryotic Translation Initiation Factor 4H (EIF4H))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser EIF4H Antikörper ist unkonjugiert

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

Produktdetails anti-EIF4H Antikörper

Kreuzreaktivität: Human

Aufreinigung: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein encompassing a sequence within the center region of human eIF4H. The exact sequence is proprietary.

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Kommentare:

Positive Control: Raji

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.63 mg/mL

Buffer: 0.1M Tris-Glycine ( pH 7), 20 % 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 EIF4H

Target: EIF4H (Eukaryotic Translation Initiation Factor 4H (EIF4H))

Andere Bezeichnung: eukaryotic translation initiation factor 4H

Hintergrund: Eukaryotic translation initiation factor 4H , WBSCR1 , WSCR1 , eIF-4H,This gene encodes one of the translation initiation factors, which functions to stimulate the initiation of protein synthesis at the level of mRNA utilization. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants. [provided by RefSeq]

Molekulargewicht: 27 kDa

Gen-ID: 7458

UniProt: Q15056

Pathways: SARS-CoV-2 Protein Interaktom