ARL13B anticorps (AA 16-428)

N° du produit ABIN7871077

Cet anticorps anti-ARL13B Polyclonal Lapin (ABIN7871077) détecte spécifiquement ARL13B dans WB, ELISA, IF, IHC (p) et FACS. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour ARL13B anticorps (AA 16-428) (ABIN7871077)

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ARL13B est non-conjugé

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

Détail du produit anti-ARL13B anticorps

Épitope: AA 16-428

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

Purification: Antigen affinity purified

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

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the ARL13B antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

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

Stock: 4 °C,-20 °C

Stockage commentaire: 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.

Détails sur ARL13B

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

Autre désignation: ARL13B

Sujet: 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