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Last updated: 2017/2/19
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COMP monoclonal antibody, clone 6G5

  • Catalog # : MAB3751
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  • Specification
  • Product Description:
  • Mouse monoclonal antibody raised against COMP.
  • Immunogen:
  • Native purified COMP from normal human cartilage.
  • Host:
  • Mouse
  • Reactivity:
  • Human
  • Specificity:
  • Reacts with both reduced and non-reduced human COMP.
  • Form:
  • Liquid
  • Isotype:
  • IgM
  • Recommend Usage:
  • ELISA (1:5-1:10)
    Western Blot (1:1-1:3)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In culture supernatant (0.01% sodium azide)
  • Storage Instruction:
  • Store at 4°C. 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
  • Immunohistochemistry (Frozen sections)
  • Immunoprecipitation
  • ELISA
  • Application Image
  • Western Blot
  • Immunohistochemistry (Frozen sections)
  • Immunoprecipitation
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 1311
  • Gene Name:
  • COMP
  • Gene Alias:
  • EDM1,EPD1,MED,MGC131819,MGC149768,PSACH,THBS5
  • Gene Description:
  • cartilage oligomeric matrix protein
  • Gene Summary:
  • The protein encoded by this gene is a noncollagenous extracellular matrix (ECM) protein. It consists of five identical glycoprotein subunits, each with EGF-like and calcium-binding (thrombospondin-like) domains. Oligomerization results from formation of a five-stranded coiled coil and disulfides. Binding to other ECM proteins such as collagen appears to depend on divalent cations. Mutations can cause the osteochondrodysplasias pseudochondroplasia (PSACH) and multiple epiphyseal dysplasia (MED). [provided by RefSeq
  • Other Designations:
  • cartilage oligomeric matrix protein (pseudoachondroplasia, epiphyseal dysplasia 1, multiple),cartilage oligomeric matrix protein(pseudoachondroplasia, epiphyseal dysplasia 1, multiple),pseudoachondroplasia (epiphyseal dysplasia 1, multiple),thrombospondin
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