ARL13B Antikörper (AA 16-428)

Produktnummer ABIN7871077

Der Kaninchen Polyklonal anti-ARL13B Antikörper (ABIN7871077) detektiert spezifisch ARL13B in WB, ELISA, IF, IHC (p) und FACS. Dieser Antikörper reagiert spezifisch mit Proben aus Human, Maus und Ratte.

Kurzübersicht für ARL13B Antikörper (AA 16-428) (ABIN7871077)

Target: ARL13B (ADP-Ribosylation Factor-Like 13B (ARL13B))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ARL13B Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)

Produktdetails anti-ARL13B Antikörper

Bindungsspezifität: AA 16-428

Verwendungszweck: ARL13B Antibody / ADP-ribosylation factor-like protein 13B

Aufreinigung: Antigen affinity purified

Immunogen: Recombinant human protein (amino acids R16-S428) was used as the immunogen for the ARL13B antibody.

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal dilution of the ARL13B antibody should be determined by the researcher.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: After reconstitution, the ARL13B antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Details zu ARL13B

Target: ARL13B (ADP-Ribosylation Factor-Like 13B (ARL13B))

Andere Bezeichnung: ARL13B

Hintergrund: ADP-ribosylation factor-like protein 13B (ARL13B), also known as ADP-ribosylation factor-like protein 2-like 1 (ARL2L1), is a protein that in humans is encoded by the ARL13B gene. This gene encodes a member of the ADP-ribosylation factor-like family. The encoded protein is a small GTPase that contains both N-terminal and C-terminal guanine nucleotide-binding motifs. This protein is localized in the cilia and plays a role in cilia formation and in maintenance of cilia. Mutations in this gene are the cause of Joubert syndrome 8. Alternate splicing results in multiple transcript variants.

UniProt: Q3SXY8