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Rhodopsin Antikörper (AA 310-339)

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch Rhodopsin in WB und ELISA. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN3032473

Kurzübersicht für Rhodopsin Antikörper (AA 310-339) (ABIN3032473)

Target

Alle Rhodopsin (RHO) Antikörper anzeigen
Rhodopsin (RHO)

Reaktivität

  • 41
  • 20
  • 17
  • 13
  • 10
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Wirt

  • 42
  • 25
  • 2
  • 1
  • 1
Kaninchen

Klonalität

  • 38
  • 32
  • 1
Polyklonal

Konjugat

  • 31
  • 6
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
Dieser Rhodopsin Antikörper ist unkonjugiert

Applikation

  • 52
  • 41
  • 39
  • 27
  • 15
  • 13
  • 10
  • 8
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA
  • Bindungsspezifität

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

    Kreuzreaktivität (Details)

    Expected species reactivity: Primate

    Aufreinigung

    Antigen affinity purified

    Immunogen

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

    Isotyp

    Ig Fraction
  • Applikationshinweise

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

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    In 1X PBS, pH 7.4, with 0.09 % sodium azide

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    -20 °C

    Informationen zur Lagerung

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

    Rhodopsin (RHO)

    Andere Bezeichnung

    rho (Rhodopsin)

    Substanzklasse

    Chemical

    Hintergrund

    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

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