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Rho-related GTP-binding protein Antikörper (C-Term)

RhO (pan) Reaktivität: Human WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN929385
  • Target Alle Rho-related GTP-binding protein (RhO (pan)) Antikörper anzeigen
    Rho-related GTP-binding protein (RhO (pan))
    Bindungsspezifität
    • 5
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    C-Term
    Reaktivität
    • 15
    • 8
    • 7
    • 7
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Wirt
    • 20
    • 9
    • 1
    Kaninchen
    Klonalität
    • 19
    • 11
    Polyklonal
    Konjugat
    • 25
    • 2
    • 2
    • 1
    Dieser Rho-related GTP-binding protein Antikörper ist unkonjugiert
    Applikation
    • 22
    • 19
    • 16
    • 6
    • 5
    • 2
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Aufreinigung
    Purified
    Immunogen
    RHO antibody was raised in rabbit using the C terminal of RHO as the immunogen
    Top Product
    Discover our top product RhO (pan) Primärantikörper
  • Applikationshinweise
    WB: 0.2-1 µg/mL
    Optimal conditions should be determined by the investigator.
    Kommentare

    RHO Blocking Peptide, catalog no. 33R-7510, is also available for use as a blocking control in assays to test for specificity of this RHO antibody

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Konzentration
    Lot specific
    Buffer
    Lyophilized powder. Add 50 µL of distilled water. Final antibody concentration is 1 mg/mL in PBS buffer.
    Handhabung
    Avoid repeated freeze/thaw cycles.
    Lagerung
    4 °C/-20 °C
    Informationen zur Lagerung
    Store at 4 °C, following reconstitution, aliquot and store at -20 °C.
  • Target
    Rho-related GTP-binding protein (RhO (pan))
    Andere Bezeichnung
    rho (RhO (pan) Produkte)
    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. Synonyms: Polyclonal RHO antibody, Anti-RHO antibody, rhodopsin antibody, CSNBAD1 antibody, MGC138309 antibody, MGC138311 antibody, OPN2 antibody, RP4 antibody.
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