Rho-related GTP-binding protein anticorps (C-Term)

N° du produit ABIN1537109

L’anticorps Lapin Polyclonal anti-Rho-related GTP-binding protein a été validé pour WB. Il convient pour détecter Rho-related GTP-binding protein dans des échantillons de Humain, Rat et Souris.

Aperçu rapide pour Rho-related GTP-binding protein anticorps (C-Term) (ABIN1537109)

Antigène: Rho-related GTP-binding protein (RhO (pan))

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Rho-related GTP-binding protein est non-conjugé

Application: Western Blotting (WB)

Clone: RB36659

Détail du produit anti-Rho-related GTP-binding protein anticorps

Épitope: AA 310-339, C-Term

Homologie: Pr

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This RHO antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 310-339 amino acids from the C-terminal region of human RHO.

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:2000. WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: RHO Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Date de péremption: 6 months

Détails sur Rho-related GTP-binding protein

Antigène: Rho-related GTP-binding protein (RhO (pan))

Autre désignation: RHO

Classe de substances: Chemical

Sujet: Retinitis pigmentosa is an inherited progressive disease which is a major cause of blindness in western communities. It can be inherited as an autosomal dominant, autosomal recessive, or X-linked recessive disorder. In the autosomal dominant form,which comprises about 25 % of total cases, approximately 30 % of families have mutations in the gene encoding the rod photoreceptor-specific protein rhodopsin. This is the transmembrane protein which, when photoexcited, initiates the visual transduction cascade. Defects in this gene are also one of the causes of congenital stationary night blindness.

Poids moléculaire: 38893

ID gène: 6010

NCBI Accession: NP_000530

UniProt: P08100