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Rho-related GTP-binding protein antibody

The Rabbit Polyclonal anti-Rho-related GTP-binding protein antibody has been validated for IHC. It is suitable to detect Rho-related GTP-binding protein in samples from Rat and Mouse.
Catalog No. ABIN7258362

Quick Overview for Rho-related GTP-binding protein antibody (ABIN7258362)

Target

See all Rho-related GTP-binding protein (RhO (pan)) Antibodies
Rho-related GTP-binding protein (RhO (pan))

Reactivity

  • 16
  • 8
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  • 5
  • 1
  • 1
  • 1
  • 1
  • 1
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Rat, Mouse

Host

  • 20
  • 9
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Rabbit

Clonality

  • 18
  • 12
Polyclonal

Conjugate

  • 25
  • 2
  • 2
  • 1
This Rho-related GTP-binding protein antibody is un-conjugated

Application

  • 23
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  • 16
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Immunohistochemistry (IHC)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    A synthetic peptide of human RHO (NP_000530.1).

    Isotype

    IgG
  • 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

    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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