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Last updated: 2016/12/4
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ADAMTS2 polyclonal antibody

  • Catalog # : PAB18817
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  • Specification
  • Product Description:
  • Rabbit polyclonal antibody raised against synthetic peptide of ADAMTS2.
  • Immunogen:
  • A synthetic peptide corresponding to 16 amino acids at C-terminus of human ADAMTS2.
  • Host:
  • Rabbit
  • Reactivity:
  • Human
  • Form:
  • Liquid
  • Purification:
  • Peptide affinity purification
  • Recommend Usage:
  • ELISA (1:1000-1:10000)
    Western Blot (1:200-1:1000)
    Immunohistochemistry (1:100-1:500)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In buffer containing 0.02% sodium azide, 0.5% BSA
  • 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 human skin lysate with ADAMTS2 polyclonal antibody (Cat # PAB18817) at 1 : 100 dilution.
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemical staining of formalin-fixed paraffin-embedded human skin tissue with ADAMTS2 polyclonal antibody (Cat # PAB18817) at 1 : 200 dilution.
  • ELISA
  • Application Image
  • Western Blot (Tissue lysate)
  • Western Blot (Tissue lysate)
  • enlarge
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • enlarge
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 9509
  • Gene Name:
  • ADAMTS2
  • Gene Alias:
  • ADAM-TS2,ADAMTS-3,NPI,PCINP,PCPNI,hPCPNI
  • Gene Description:
  • ADAM metallopeptidase with thrombospondin type 1 motif, 2
  • Gene Summary:
  • This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The enzyme encoded by this gene excises the N-propeptide of type I, type II and type V procollagens. Mutations in this gene cause Ehlers-Danlos syndrome type VIIC, a recessively inherited connective-tissue disorder. Alternative splicing results in two transcript variants. The short transcript encodes a protein which has no significant procollagen N-peptidase activity. [provided by RefSeq
  • Other Designations:
  • a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 2,procollagen I N-proteinase,procollagen N-endopeptidase
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