Telefon:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@antikoerper-online.de

Rho-related GTP-binding protein Antikörper

RhO (pan) Reaktivität: Human WB, IHC Wirt: Kaninchen Monoclonal unconjugated
Produktnummer ABIN7269974
  • Target Alle Rho-related GTP-binding protein (RhO (pan)) Antikörper anzeigen
    Rho-related GTP-binding protein (RhO (pan))
    Reaktivität
    • 17
    • 8
    • 8
    • 5
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Wirt
    • 22
    • 4
    • 1
    Kaninchen
    Klonalität
    • 23
    • 4
    Monoklonal
    Konjugat
    • 18
    • 3
    • 2
    • 2
    • 1
    • 1
    Dieser Rho-related GTP-binding protein Antikörper ist unkonjugiert
    Applikation
    • 20
    • 18
    • 10
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    Verwendungszweck
    Rhodopsin Rabbit mAb
    Kreuzreaktivität
    Maus, Ratte
    Produktmerkmale
    Monoclonal Antibodies
    Aufreinigung
    Affinity purification
    Immunogen
    A synthesized peptide derived from human Rhodopsin
    Isotyp
    IgG
    Top Product
    Discover our top product RhO (pan) Primärantikörper
  • Applikationshinweise
    WB,1:500 - 1:2000,IHC,1:50 - 1:200
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.
    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
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    Rho-related GTP-binding protein (RhO (pan))
    Andere Bezeichnung
    RHO (RhO (pan) Produkte)
    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. [provided by RefSeq, Jul 2008],CSNBAD1, OPN2, RP4,G protein signaling,G protein signaling_G-Protein-Coupled Receptors(GPCR),Neuroscience,Signal Transduction,RHO
    Molekulargewicht
    39kDa
    Gen-ID
    6010
    UniProt
    P08100
Sie sind hier:
Kundenservice