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

RhO (pan) Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN929385
  • Target See all Rho-related GTP-binding protein (RhO (pan)) Antibodies
    Rho-related GTP-binding protein (RhO (pan))
    Binding Specificity
    • 5
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    C-Term
    Reactivity
    • 15
    • 8
    • 7
    • 7
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 20
    • 9
    • 1
    Rabbit
    Clonality
    • 19
    • 11
    Polyclonal
    Conjugate
    • 25
    • 2
    • 2
    • 1
    This Rho-related GTP-binding protein antibody is un-conjugated
    Application
    • 22
    • 19
    • 16
    • 6
    • 5
    • 2
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Purification
    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) Primary Antibody
  • Application Notes
    WB: 0.2-1 µg/mL
    Optimal conditions should be determined by the investigator.
    Comment

    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

    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Concentration
    Lot specific
    Buffer
    Lyophilized powder. Add 50 µL of distilled water. Final antibody concentration is 1 mg/mL in PBS buffer.
    Handling Advice
    Avoid repeated freeze/thaw cycles.
    Storage
    4 °C/-20 °C
    Storage Comment
    Store at 4 °C, following reconstitution, aliquot and store at -20 °C.
  • Target
    Rho-related GTP-binding protein (RhO (pan))
    Alternative Name
    rho (RhO (pan) Products)
    Target Type
    Chemical
    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. Synonyms: Polyclonal RHO antibody, Anti-RHO antibody, rhodopsin antibody, CSNBAD1 antibody, MGC138309 antibody, MGC138311 antibody, OPN2 antibody, RP4 antibody.
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