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Last updated: 2014/4/14
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BIOtech
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TIMP3 polyclonal antibody

  • Catalog # : PAB11828
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  • Specification
  • Product Description:
  • Rabbit polyclonal antibody raised against synthetic peptide of TIMP3.
  • Immunogen:
  • A synthetic peptide corresponding to C-terminus of human TIMP3.
  • Host:
  • Rabbit
  • Theoretical MW (kDa):
  • 23
  • Reactivity:
  • Human
  • Form:
  • Liquid
  • Purification:
  • Immunoaffinity purification
  • Concentration:
  • Lot specific
  • Quality Control Testing:
  • Antibody Reactive Against Synthetic Peptide.
  • Recommend Usage:
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (Formalin/PFA-fixed paraffin-embedded sections) (1:70)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In 10 mM PBS, pH 7.4 (1% BSA, 0.1% sodium azide)
  • Storage Instruction:
  • Store at 4°C.
  • 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)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemical staining of TIMP3 on formalin fixed, paraffin embedded human placenta with TIMP3 polyclonal antibody (Cat # PAB11828).
  • Application Image
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • enlarge
  • Gene Information
  • Entrez GeneID:
  • 7078
  • Gene Name:
  • TIMP3
  • Gene Alias:
  • HSMRK222,K222,K222TA2,SFD
  • Gene Description:
  • TIMP metallopeptidase inhibitor 3
  • Gene Summary:
  • This gene belongs to the TIMP gene family. The proteins encoded by this gene family are inhibitors of the matrix metalloproteinases, a group of peptidases involved in degradation of the extracellular matrix (ECM). Expression of this gene is induced in response to mitogenic stimulation and this netrin domain-containing protein is localized to the ECM. Mutations in this gene have been associated with the autosomal dominant disorder Sorsby's fundus dystrophy. [provided by RefSeq
  • Other Designations:
  • MIG-5 protein,tissue inhibitor of metalloproteinase 3
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