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Last updated: 2016/12/11

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RHO purified MaxPab mouse polyclonal antibody (B01P)MaxPab

  • Catalog # : H00006010-B01P
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  • Specification
  • Product Description:
  • Mouse polyclonal antibody raised against a full-length human RHO protein.
  • Immunogen:
  • RHO (CAL37658.1, 1 a.a. ~ 348 a.a) full-length human protein.
  • Sequence:
  • MNGTEGPNFYVPFSNATGVVRSPFEYPQYYLAEPWQFSMLAAYMFLLIVLGFPINFLTLYVTVQHKKLRTPLNYILLNLAVADLFMVLGGFTSTLYTSLHGYFVFGPTGCNLEGFFATLGGEIALWSLVVLAIERYVVVCKPMSNFRFGENHAIMGVAFTWVMALACAAPPLAGWSRYIPEGLQCSCGIDYYTLKPEVNNESFVIYMFVVHFTIPMIIIFFCYGQLVFTVKEAAAQQQESATTQKAEKEVTRMVIIMVIAFLICWVPYASVAFYIFTHQGSNFGPIFMTIPAFFAKSAAIYNPVIYIMMNKQFRNCMLTTICCGKNPLGDDEASATVSKTETSQVAPA
  • Host:
  • Mouse
  • Reactivity:
  • Human
  • Quality Control Testing:
  • Antibody reactive against mammalian transfected lysate.
  • Storage Buffer:
  • In 1x PBS, pH 7.4
  • Storage Instruction:
  • Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
  • Applications
  • Application Image
  • Western Blot (Transfected lysate)
  • 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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