RHO (phospho S188) polyclonal antibody

Catalog # PAB12644

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Size:100 ug
Price: USD $ 346.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
  • Specifications

    Product Description

    Rabbit polyclonal antibody raised against synthetic phosphopeptide of RHO.

    Immunogen

    Synthetic phosphopeptide corresponding to residues surrounding S188 of human RHO.

    Sequence

    KKKSG

    Host

    Rabbit

    Theoretical MW (kDa)

    24

    Reactivity

    Human, Mouse, Rat

    Specificity

    This antibody recognizes ~24 KDa of human RHO.

    Form

    Liquid

    Quality Control Testing

    Antibody Reactive Against Synthetic Peptide.

    Recommend Usage

    Western Blot (0.1-1 ug/mL)
    ELISA (0.01-0.1 ug/mL)
    Immunoprecipitation (2-5 ug/mL)
    Immunohistochemistry (2-10 ug/mL)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In TBS, pH 7.2 (BSA, 10% Proclin300)

    Storage Instruction

    Store at 4°C. For long term storage store at -20°C to -80°C.
    Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot

    Immunohistochemistry

    Immunoprecipitation

    Enzyme-linked Immunoabsorbent Assay

  • Gene Info — RHO

    Entrez GeneID

    6010

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