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

Der Kaninchen Monoklonal Anti-Rho-related GTP-binding protein-Antikörper wurde für WB und IHC validiert. Er ist geeignet, Rho-related GTP-binding protein in Proben von Human zu detektieren.
Produktnummer ABIN7269974

Kurzübersicht für Rho-related GTP-binding protein Antikörper (ABIN7269974)

Target

Alle Rho-related GTP-binding protein (RhO (pan)) Antikörper anzeigen
Rho-related GTP-binding protein (RhO (pan))

Reaktivität

  • 15
  • 8
  • 8
  • 7
  • 5
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 20
  • 9
  • 1
Kaninchen

Klonalität

  • 19
  • 11
Monoklonal

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), 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
  • 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

    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:
Chat with us!