VSX1 anticorps

N° du produit ABIN7232124

Cet anticorps anti-VSX1 est un anticorps Lapin Polyclonal détectant VSX1 dans WB et ELISA. Adapté pour Humain et Souris.

Aperçu rapide pour VSX1 anticorps (ABIN7232124)

Antigène: VSX1 (Visual System Homeobox 1 (VSX1))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp VSX1 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-VSX1 anticorps

Fonction: VSX1 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of VSX1 protein

Purification: The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

Immunogène: Synthesized peptide derived from part region of human VSX1 protein

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

Commentaires:

Primary Antibody

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

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: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Détails sur VSX1

Antigène: VSX1 (Visual System Homeobox 1 (VSX1))

Autre désignation: VSX1

Sujet: Rabbit Anti-VSX1 Polyclonal Antibody,Visual system homeobox 1, Homeodomain protein RINX, Retinal inner nuclear layer homeobox protein, Transcription factor VSX1,VSX1 encoded by this gene contains a paired-like homeodomain and binds to the core of the locus control region of the red/green visual pigment gene cluster. The encoded protein may regulate expression of the cone opsin genes early in development. Mutations in this gene can cause posterior polymorphous corneal dystrophy and keratoconus. Alternatively spliced transcript variants encoding different isoforms have been described. VSX1 (Visual System Homeobox 1) is a Protein Coding gene. Diseases associated with VSX1 include Keratoconus 1 and Craniofacial Anomalies And Anterior Segment Dysgenesis Syndrome.,VSX1

Poids moléculaire: observerd band 40kDa

ID gène: 30813

UniProt: Q9NZR4