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VSX1 anticorps (Middle Region)

Cet anticorps anti-VSX1 est un anticorps Lapin Polyclonal détectant VSX1 dans WB et EIA. Adapté pour Humain.
N° du produit ABIN955533

Aperçu rapide pour VSX1 anticorps (Middle Region) (ABIN955533)

Antigène

Voir toutes VSX1 Anticorps
VSX1 (Visual System Homeobox 1 (VSX1))

Reactivité

  • 25
  • 7
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Humain

Hôte

  • 27
Lapin

Clonalité

  • 27
Polyclonal

Conjugué

  • 15
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp VSX1 est non-conjugé

Application

Western Blotting (WB), Enzyme Immunoassay (EIA)
  • Épitope

    • 8
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 124-154, Middle Region

    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
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • 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.
  • Antigène

    VSX1 (Visual System Homeobox 1 (VSX1))

    Autre désignation

    VSX1 / RINX

    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
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