OVOL2 anticorps (AA 90-170)

N° du produit ABIN7230428

L’anticorps anti-OVOL2 Polyclonal Lapin est utilisé pour la détection de OVOL2 dans des échantillons de Humain et Souris. Il a été validé pour WB et ELISA.

Aperçu rapide pour OVOL2 anticorps (AA 90-170) (ABIN7230428)

Antigène: OVOL2 (Ovo-Like 2 (OVOL2))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp OVOL2 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-OVOL2 anticorps

Épitope: AA 90-170

Fonction: Rabbit Anti-OVOL2 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of OVOL2 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 OVOL2 protein at AA range: 90-170

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 OVOL2

Antigène: OVOL2 (Ovo-Like 2 (OVOL2))

Autre désignation: OVOL2

Sujet: Transcription factor Ovo-like 2, hOvo2, Zinc finger protein 339OVOL2 encodes a member of the evolutionarily conserved ovo-like protein family. Mammalian members of this family contain a single zinc finger domain composed of a tetrad of C2H2 zinc fingers with variable N- and C-terminal extensions that contain intrinsically disordered domains. Members of this family are involved in epithelial development and differentiation. Knockout of this gene in mouse results in early embryonic lethality with phenotypes that include neurectoderm expansion, impaired vascularization, and heart anomalies. In humans, allelic variants of OVOL2 have been associated with posterior polymorphous corneal dystrophy.

Poids moléculaire: 30kD

ID gène: 58495

UniProt: Q9BRP0

Pathways: Tube Formation