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CRX anticorps (AA 265-299)

L’anticorps Lapin Polyclonal anti-CRX a été validé pour WB. Il convient pour détecter CRX dans des échantillons de Humain.
N° du produit ABIN5647525

Aperçu rapide pour CRX anticorps (AA 265-299) (ABIN5647525)

Antigène

Voir toutes CRX Anticorps
CRX (Cone-Rod Homeobox (CRX))

Reactivité

  • 26
  • 24
  • 23
Humain

Hôte

  • 32
  • 7
  • 1
  • 1
Lapin

Clonalité

  • 34
  • 7
Polyclonal

Conjugué

  • 17
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp CRX est non-conjugé

Application

  • 18
  • 13
  • 13
  • 11
  • 4
  • 4
  • 4
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 15
    • 5
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 265-299

    Purification

    Antigen affinity purified

    Immunogène

    Amino acids 265-299 (DSLEFKDPTGTWKFTYNPMDPLDYKDQSAWKFQIL) from the human protein were used as the immunogen for the CRX antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the CRX antibody should be determined by the researcher.\. WB: 0.5-1 μg/mL

    Restrictions

    For Research Use only
  • Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Stock

    -20 °C

    Stockage commentaire

    After reconstitution, the CRX antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Antigène

    CRX (Cone-Rod Homeobox (CRX))

    Autre désignation

    CRX (Cone-rod homeobox)

    Sujet

    Cone-rod homeobox protein is a protein that in humans is encoded by the CRX gene. The protein encoded by this gene is a photoreceptor-specific transcription factor which plays a role in the differentiation of photoreceptor cells. This homeodomain protein is necessary for the maintenance of normal cone and rod function. Mutations in this gene are associated with photoreceptor degeneration, Leber congenital amaurosis type III and the autosomal dominant cone-rod dystrophy 2. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some variants has not been determined.

    UniProt

    O43186
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