AHI1 Antikörper (N-Term)

Produktnummer ABIN2854592

Der Kaninchen Polyklonal Anti-AHI1-Antikörper wurde für WB validiert. Er ist geeignet, AHI1 in Proben von Human zu detektieren.

Kurzübersicht für AHI1 Antikörper (N-Term) (ABIN2854592)

Target: AHI1 (Abelson Helper Integration Site 1 (AHI1))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser AHI1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-AHI1 Antikörper

Bindungsspezifität: N-Term

Kreuzreaktivität: Human

Produktmerkmale: Rabbit Polyclonal antibody to AHI1 (Abelson helper integration site 1)
AHI1 antibody [N1], N-term

Aufreinigung: Purified by antigen-affinity chromatography.

Immunogen: Carrier-protein conjugated synthetic peptide encompassing a sequence within the N-terminus region of human AHI1. 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: NT2D1

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 AHI1

Target: AHI1 (Abelson Helper Integration Site 1 (AHI1))

Andere Bezeichnung: Abelson helper integration site 1

Hintergrund: This gene is apparently required for both cerebellar and cortical development in humans. This gene mutations cause specific forms of Joubert syndrome-related disorders. Joubert syndrome (JS) is a recessively inherited developmental brain disorder with several identified causative chromosomal loci. Alternatively spliced transcript variants encoding different isoforms have been identified.

Molekulargewicht: 137 kDa

Gen-ID: 54806

UniProt: Q8N157