RAX2 anticorps (C-Term) (FITC)

N° du produit ABIN8031690

L’anticorps anti-RAX2 Polyclonal Lapin est utilisé pour la détection de RAX2 dans des échantillons de Humain. Il a été validé pour FACS.

Aperçu rapide pour RAX2 anticorps (C-Term) (FITC) (ABIN8031690)

Antigène: RAX2 (Retina and Anterior Neural Fold Homeobox 2 (RAX2))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp RAX2 est conjugé à/à la FITC

Application: Flow Cytometry (FACS)

Détail du produit anti-RAX2 anticorps (FITC)

Épitope: C-Term

Fonction: Anti-RAX2 Antibody FITC Conjugated

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

Purification: Immunogen affinity purified.

Immunogène: A synthetic peptide corresponding to a sequence at the C-terminus of human RAX2.

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 RAX2

Antigène: RAX2 (Retina and Anterior Neural Fold Homeobox 2 (RAX2))

Autre désignation: RAX2

Sujet:

Background: This gene encodes a homeodomain-containing protein that plays a role in eye development. Mutation of this gene causes age-related macular degeneration type 6, an eye disorder resulting in accumulations of protein and lipid beneath the retinal pigment epithelium and within the Bruch's membrane. Defects in this gene can also cause cone-rod dystrophy type 11, a disease characterized by the initial degeneration of cone photoreceptor cells and resulting in loss of color vision and visual acuity, followed by the degeneration of rod photoreceptor cells, which progresses to night blindness and the loss of peripheral vision. Alternative splicing results in multiple transcript variants.

Gene Full Name: retina and anterior neural fold homeobox 2

ID gène: 84839

UniProt: Q96IS3