RRBP1 anticorps (AA 1289-1400)

N° du produit ABIN7870419

L’anticorps anti-RRBP1 Polyclonal Lapin est utilisé pour la détection de RRBP1 dans des échantillons de Humain. Il a été validé pour WB, ELISA, FACS, IF et IHC (p).

Aperçu rapide pour RRBP1 anticorps (AA 1289-1400) (ABIN7870419)

Antigène: RRBP1 (Ribosome Binding Protein 1 (RRBP1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp RRBP1 est non-conjugé

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

Détail du produit anti-RRBP1 anticorps

Épitope: AA 1289-1400

Fonction: Ribosome binding protein 1 Antibody / RRBP1

Purification: Antigen affinity purified

Immunogène: An E.coli-derived human recombinant protein (amino acids Q1289-D1400) was used as the immunogen for the Ribosome binding protein 1 antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the Ribosome binding protein 1 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 Ribosome binding protein 1 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 RRBP1

Antigène: RRBP1 (Ribosome Binding Protein 1 (RRBP1))

Autre désignation: Ribosome binding protein 1

Sujet: Ribosome-binding protein 1, also referred to as p180, is a protein that in humans is encoded by the RRBP1 gene. It is mapped to 20p12.1. This gene encodes a ribosome-binding protein of the endoplasmic reticulum (ER) membrane. Studies suggest that this gene plays a role in ER proliferation, secretory pathways and secretory cell differentiation, and mediation of ER-microtubule interactions. Alternative splicing has been observed and protein isoforms are characterized by regions of N-terminal decapeptide and C-terminal heptad repeats. Splicing of the tandem repeats results in variations in ribosome-binding affinity and secretory function. The full-length nature of variants which differ in repeat length has not been determined. Pseudogenes of this gene have been identified on chromosomes 3 and 7, and RRBP1 has been excluded as a candidate gene in the cause of Alagille syndrome, the result of a mutation in a nearby gene on chromosome 20p12.

UniProt: Q9P2E9