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RHO polyclonal antibody

  • Catalog # : PAB26439
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  • Specification
  • Product Description:
  • Rabbit polyclonal antibody raised against synthetic peptide of RHO.
  • Immunogen:
  • A synthetic peptide corresponding to 19 amino acids at 2nd extracellular domain of human RHO.
  • Host:
  • Rabbit
  • Reactivity:
  • Human, Monkey, Mouse, Pig, Rabbit, Rat
  • Specificity:
  • BLAST analysis of the peptide immunogen showed no homology with other human proteins.
  • Form:
  • Liquid
  • Purification:
  • Immunoaffinity chromatography
  • Recommend Usage:
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (1-3 ug/mL)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In PBS (0.09% sodium azide)
  • Storage Instruction:
  • Store at 4°C. For long term storage store at -80°C.
    Aliquot to 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
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunocytochemistry
  • Immunocytochemistry
  • Immunocytochemistry (ICC) staining of HEK293 human embryonic kidney cells transfected (A) or untransfected (B) with RHO. Using RHO polyclonal antibody (Cat # PAB26439).
  • Application Image
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • 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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