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

RhO (pan) Reactivity: Human, Mouse, Rat WB Host: Rabbit Polyclonal RB36659 unconjugated
Catalog No. ABIN1537109
  • Target See all Rho-related GTP-binding protein (RhO (pan)) Antibodies
    Rho-related GTP-binding protein (RhO (pan))
    Binding Specificity
    • 8
    • 6
    • 5
    • 2
    • 1
    • 1
    • 1
    AA 310-339, C-Term
    Reactivity
    • 17
    • 7
    • 7
    • 5
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 22
    • 4
    • 1
    Rabbit
    Clonality
    • 22
    • 5
    Polyclonal
    Conjugate
    • 18
    • 3
    • 2
    • 2
    • 1
    • 1
    This Rho-related GTP-binding protein antibody is un-conjugated
    Application
    • 20
    • 18
    • 11
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Predicted Reactivity
    Pr
    Purification
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    Immunogen
    This RHO antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 310-339 amino acids from the C-terminal region of human RHO.
    Clone
    RB36659
    Isotype
    Ig Fraction
    Top Product
    Discover our top product RhO (pan) Primary Antibody
  • Application Notes
    WB: 1:2000. WB: 1:1000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    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
    4 °C,-20 °C
    Storage Comment
    RHO Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.
    Expiry Date
    6 months
  • 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.
    Molecular Weight
    38893
    Gene ID
    6010
    NCBI Accession
    NP_000530
    UniProt
    P08100
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