RPGRIP1L anticorps (AA 608-1264)

N° du produit ABIN7876102

Cet anticorps anti-RPGRIP1L Polyclonal Lapin (ABIN7876102) détecte spécifiquement RPGRIP1L dans WB, ELISA et FACS. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour RPGRIP1L anticorps (AA 608-1264) (ABIN7876102)

Antigène: RPGRIP1L (RPGRIP1-Like (RPGRIP1L))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp RPGRIP1L est non-conjugé

Application: Western Blotting (WB), ELISA, Flow Cytometry (FACS)

Détail du produit anti-RPGRIP1L anticorps

Épitope: AA 608-1264

Fonction: RPGRIP1L Antibody / Protein fantom

Purification: Antigen affinity purified

Immunogène: E. coli-derived recombinant human protein (amino acids E608-D1264) was used as the immunogen for the RPGRIP1L antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the RPGRIP1L 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 RPGRIP1L 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 RPGRIP1L

Antigène: RPGRIP1L (RPGRIP1-Like (RPGRIP1L))

Autre désignation: RPGRIP1L

Sujet: The protein encoded by this gene can localize to the basal body-centrosome complex or to primary cilia and centrosomes in ciliated cells. The encoded protein has been found to interact with nephrocystin-4. Defects in this gene are a cause of Joubert syndrome type 7 (JBTS7) and Meckel syndrome type 5 (MKS5).

UniProt: Q68CZ1

Pathways: DNA Replication, Regulation of G-Protein Coupled Receptor Protein Signaling, Synthesis of DNA