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Last updated: 2016/9/25
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RHO polyclonal antibody

  • Catalog # : PAB12727
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  • Specification
  • Product Description:
  • Rabbit polyclonal antibody raised against synthetic peptide of RHO.
  • Immunogen:
  • A synthetic peptide corresponding to C-terminus of human RHO.
  • Host:
  • Rabbit
  • Theoretical MW (kDa):
  • 24
  • Reactivity:
  • Human, Mouse, Rat
  • Specificity:
  • This antibody recognizes ~24 KDa of human RHO.
  • Form:
  • Liquid
  • Isotype:
  • IgG
  • Recommend Usage:
  • Western Blot (0.1-1 ug/mL)
    ELISA (0.01-0.1 ug/mL)
    Immunoprecipitation (2-5 ug/mL)
    Immunohistochemistry (2-5 ug/mL)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In PBS, pH 7.2 (BSA, 10% Proclin300)
  • Storage Instruction:
  • Store at 4°C. For long term storage store at -20°C or -80°C.
    Aliquot to avoid repeated freezing and thawing.
  • Publication Reference
  • Applications
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • The cell lysate derived from MCF-7 was immunoprobed by RHO polyclonal antibody (Cat # PAB12727) at 1 : 500. An immunoreactive band is observed around ~24 kDa (2). This band is abolished by pre-incubation with immunizing peptide (1).
  • Immunohistochemistry
  • Immunoprecipitation
  • ELISA
  • Application Image
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • enlarge
  • Immunohistochemistry
  • Immunoprecipitation
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 6010
  • Gene Name:
  • RHO
  • Gene Alias:
  • CSNBAD1,MGC138309,MGC138311,OPN2,RP4
  • Gene Description:
  • rhodopsin
  • 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)
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