CRX anticorps (C-Term) (Fluoro594)

N° du produit ABIN7981595

Cet anticorps anti-CRX Polyclonal Lapin conjugué à Fluoro594 (ABIN7981595) détecte spécifiquement CRX dans FACS. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour CRX anticorps (C-Term) (Fluoro594) (ABIN7981595)

Antigène: CRX (Cone-Rod Homeobox (CRX))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CRX est conjugé à/à la Fluoro594

Application: Flow Cytometry (FACS)

Détail du produit anti-CRX anticorps (Fluoro594)

Épitope: C-Term

Fonction: Anti-CORD2/CRX Antibody Fluoro594 Conjugated

Specificité: No cross reactivity with other proteins.

Réactivité croisée (Details): No cross-reactivity with other proteins.

Homologie: identical to the related mouse,rat sequences.

Purification: Immunogen affinity purified.

Immunogène: A synthetic peptide corresponding to a sequence at the C-terminus of human CORD2, identical to the related mouse and rat sequences.

Isotype: IgG

Information d'application

Indications d'application: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % 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: -20 °C

Stockage commentaire: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Date de péremption: 12 months

Détails sur CRX

Antigène: CRX (Cone-Rod Homeobox (CRX))

Autre désignation: CRX

Sujet:

Background: Cone-rod homeobox protein is a protein that in humans is encoded by the CRX gene. The protein encoded by this gene is a photoreceptor-specific transcription factor which plays a role in the differentiation of photoreceptor cells. This homeodomain protein is necessary for the maintenance of normal cone and rod function. Mutations in this gene are associated with photoreceptor degeneration, Leber congenital amaurosis type III and the autosomal dominant cone-rod dystrophy 2. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some variants has not been determined.

Gene Full Name: cone-rod homeobox

ID gène: 1406

UniProt: O43186