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KIAA0196 polyclonal antibody

  • Catalog # : PAB25762
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  • Specification
  • Product Description:
  • Rabbit polyclonal antibody raised against synthetic peptide of KIAA0196.
  • Immunogen:
  • A synthetic peptide corresponding to 19 amino acids at C-terminus of human KIAA0196.
  • Host:
  • Rabbit
  • Reactivity:
  • Human, Mouse, Rat
  • Specificity:
  • Multiple isoforms of Strumpellin are known to exist.
  • Form:
  • Liquid
  • Purification:
  • Peptide affinity purification
  • Concentration:
  • 1 mg/mL
  • Isotype:
  • IgG
  • Recommend Usage:
  • Western Blot (1 ug/mL)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In PBS (0.02% sodium azide)
  • Storage Instruction:
  • Store at 4°C for three months. For long term storage store at -20°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
  • Western Blot (Tissue lysate)
  • Western Blot (Tissue lysate)
  • Western blot analysis of KIAA0196 in human ovary tissue with KIAA0196 polyclonal antibody (Cat # PAB25762) at 1 ug/mL.
  • ELISA
  • Application Image
  • Western Blot (Tissue lysate)
  • Western Blot (Tissue lysate)
  • enlarge
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 9897
  • Gene Name:
  • KIAA0196
  • Gene Alias:
  • MGC111053,SPG8
  • Gene Description:
  • KIAA0196
  • Gene Summary:
  • This gene encodes a 134 kDa protein named strumpellin that is predicted to have multiple transmembrane domains and a spectrin-repeat-containing domain. This ubiquitously expressed gene has its highest expression in skeletal muscle. The protein is named for Strumpell disease; a form of hereditary spastic paraplegia (HSP). Spastic paraplegias are a diverse group of disorders in which the autosomal dominant forms are characterized by progressive, lower extremity spasticity caused by axonal degeneration in the terminal portions of the longest descending and ascending corticospinal tracts. More than 30 loci (SPG1-33) have been implicated in hereditary spastic paraplegia diseases. [provided by RefSeq
  • Other Designations:
  • spastic paraplegia 8 (autosomal dominant),strumpellin
  • Related Disease
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