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Rhodopsin anticorps (AA 310-339)

Cet anticorps Lapin Polyclonal détecte spécifiquement Rhodopsin dans WB et ELISA. Il présente une réactivité envers Humain.
N° du produit ABIN3032473

Aperçu rapide pour Rhodopsin anticorps (AA 310-339) (ABIN3032473)

Antigène

Voir toutes Rhodopsin (RHO) Anticorps
Rhodopsin (RHO)

Reactivité

  • 41
  • 19
  • 17
  • 13
  • 10
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Humain

Hôte

  • 41
  • 25
  • 2
  • 1
  • 1
Lapin

Clonalité

  • 37
  • 32
  • 1
Polyclonal

Conjugué

  • 30
  • 6
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
Cet anticorp Rhodopsin est non-conjugé

Application

  • 51
  • 41
  • 38
  • 26
  • 14
  • 13
  • 10
  • 8
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA
  • Épitope

    • 6
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 310-339

    Réactivité croisée (Details)

    Expected species reactivity: Primate

    Purification

    Antigen affinity purified

    Immunogène

    A portion of amino acids 310-339 from human Rhodopsin was used as the immunogen for this RHO antibody.

    Isotype

    Ig Fraction
  • Indications d'application

    Titration of the RHO antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    In 1X PBS, pH 7.4, with 0.09 % 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.

    Stock

    -20 °C

    Stockage commentaire

    Aliquot the RHO antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • Antigène

    Rhodopsin (RHO)

    Autre désignation

    rho (Rhodopsin)

    Classe de substances

    Chemical

    Sujet

    Retinitis pigmentosa is an inherited progressive disease which is a major cause of blindness in western communities. It can be inherited as an autosomal dominant, autosomal recessive, or X-linked recessive disorder. In the autosomal dominant form,which comprises about 25 % of total cases, approximately 30 % of families have mutations in the gene encoding the rod photoreceptor-specific protein rhodopsin. This is the transmembrane protein which, when photoexcited, initiates the visual transduction cascade. Defects in this gene are also one of the causes of congenital stationary night blindness.

    UniProt

    P08100

    Pathways

    Signalisation WNT, Sensory Perception of Sound, Regulation of G-Protein Coupled Receptor Protein Signaling, Phototransduction
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