RHO monoclonal antibody, clone AADI-18

Catalog # MAB20675

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Size:100 uL
Price: USD $ 428.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Western Blot (Tissue lysate)
Application

Western Blot (Tissue lysate)

Western Blot analysis of rat eyeball tissue lysate with RHO monoclonal antibody, clone AADI-18 (Cat # MAB20675).

  • Specifications

    Product Description

    Rabbit monoclonal antibody raised against synthetic peptide of human RHO.

    Immunogen

    A synthetic peptide corresponding to human RHO.

    Host

    Rabbit

    Theoretical MW (kDa)

    38.893

    Reactivity

    Human

    Form

    Liquid

    Purification

    Affinity purification

    Isotype

    IgG

    Recommend Usage

    Immunohistochemistry (1:50-1:200)
    Western Blot (1:500-1:2000)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In PBS, 150 mM NaCl, pH 7.4 (50% glycerol, 0.02% sodium azide).

    Storage Instruction

    Store at -20°C for one year. After reconstitution, at 4°C for one month. It can also be aliquotted and stored frozen at -20°C for a longer time. Avoid repeated freezing and thawing.

    Note

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

  • Applications

    Western Blot (Tissue lysate)

    Western Blot analysis of rat eyeball tissue lysate with RHO monoclonal antibody, clone AADI-18 (Cat # MAB20675).

    Immunohistochemistry

  • Gene Info — RHO

    Entrez GeneID

    6010

    Protein Accession#

    P08100

    Gene Name

    RHO

    Gene Alias

    CSNBAD1, MGC138309, MGC138311, OPN2, RP4

    Gene Description

    rhodopsin

    Omim ID

    180380

    Gene Ontology

    Hyperlink

    Gene Summary

    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

    Other Designations

    opsin 2, rod pigment|retinitis pigmentosa 4, autosomal dominant|rhodopsin (opsin 2, rod pigment) (retinitis pigmentosa 4, autosomal dominant)

  • Interactomes
  • Diseases
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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