VSX1 anticorps (Middle Region)

N° du produit ABIN955533

Détail du produit anti-VSX1 anticorps

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

Épitope: AA 124-154, Middle Region

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp VSX1 est non-conjugé

Application: Western Blotting (WB), Enzyme Immunoassay (EIA)

Specificité: This anibody detects VSX1 / RINX (Center).

Réactivité croisée (Details): Species reactivity (tested):Human

Purification: Protein A column followed by peptide affinity purification

Immunogène: KLH conjugated synthetic peptide between 124-154 amino acids from the Central region of human VSX1

Isotype: Ig Fraction

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: PBS with 0.09 % (W/V) 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.

Conseil sur la manipulation: Avoid repeated freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store at 2 - 8 °C for up to six months or (in aliquots) at -20 °C for longer.

Détails sur VSX1

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

Autre désignation: VSX1 / RINX (VSX1 Produits)

Synonymes: anticorps VSX1, anticorps CAASDS, anticorps KTCN, anticorps KTCN1, anticorps PPCD, anticorps PPD, anticorps RINX, anticorps CHX10-1, anticorps CHX10-like, anticorps visual system homeobox 1, anticorps visual system homeobox 1 L homeolog, anticorps visual system homeobox 1 homolog, chx10-like, anticorps Vsx1, anticorps VSX1, anticorps Tsp_01485, anticorps vsx1.L, anticorps vsx1

Sujet: VSX1 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.Synonyms: Homeodomain protein RINX, Retinal inner nuclear layer homeobox protein, Visual system homeobox 1

ID gène: 30813

NCBI Accession: NP_055403