VSX2 anticorps (AA 70-150)

N° du produit ABIN7232126

L’anticorps anti-VSX2 Polyclonal Lapin est utilisé pour la détection de VSX2 dans des échantillons de Humain et Souris. Il a été validé pour WB et ELISA.

Aperçu rapide pour VSX2 anticorps (AA 70-150) (ABIN7232126)

Antigène: VSX2 (Visual System Homeobox 2 (VSX2))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp VSX2 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-VSX2 anticorps

Épitope: AA 70-150

Fonction: Rabbit Anti-VSX2 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of VSX2 protein

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogène: Synthesized peptide derived from part region of human VSX2 protein at AA range: 70-150

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 1:500-2000,ELISA 1:5000-20000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: 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.

Date de péremption: 12 months

Détails sur VSX2

Antigène: VSX2 (Visual System Homeobox 2 (VSX2))

Autre désignation: VSX2

Sujet: Visual system homeobox 2, Ceh-10 homeodomain-containing homolog Homeobox protein CHX10VSX2 (Visual System Homeobox 2) is a Protein Coding gene. Diseases associated with VSX2 include Microphthalmia, Isolated 2 and Microphthalmia With Coloboma 3. VSX2 encodes a homeobox protein originally described as a retina-specific transcription factor. Mutations in VSX2 are associated with microphthalmia, cataracts and iris abnormalities.

Poids moléculaire: 39kD

ID gène: 338917

UniProt: P58304

Pathways: Dopaminergic Neurogenesis