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Rho-related GTP-binding protein antibody

RhO (pan) Reactivity: Mouse, Rat IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7258362
  • Target See all Rho-related GTP-binding protein (RhO (pan)) Antibodies
    Rho-related GTP-binding protein (RhO (pan))
    Reactivity
    • 19
    • 9
    • 9
    • 6
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Mouse, Rat
    Host
    • 23
    • 7
    • 1
    Rabbit
    Clonality
    • 23
    • 8
    Polyclonal
    Conjugate
    • 22
    • 3
    • 2
    • 2
    • 1
    • 1
    This Rho-related GTP-binding protein antibody is un-conjugated
    Application
    • 24
    • 19
    • 13
    • 5
    • 5
    • 4
    • 4
    • 2
    Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    A synthetic peptide of human RHO (NP_000530.1).
    Isotype
    IgG
    Top Product
    Discover our top product RhO (pan) Primary Antibody
  • Application Notes
    IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    Rho-related GTP-binding protein (RhO (pan))
    Alternative Name
    RHO (RhO (pan) Products)
    Background
    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.
    Gene ID
    6010
    UniProt
    P08100
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