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Last updated: 2021/6/13

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THBD monoclonal antibody, clone 2C6C3 

  • Catalog # : MAB21380
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  • Specification
  • Product Description:
  • Mouse monoclonal antibody raised against partial recombinant human THBD.
  • Immunogen:
  • Recombinant protein corresponding to amino acids 297-505 of human THBD.
  • Host:
  • Mouse
  • Theoretical MW (kDa):
  • 60.3
  • Reactivity:
  • Human
  • Form:
  • Liquid
  • Isotype:
  • IgG1
  • Recommend Usage:
  • ELISA (1:10000)
    Flow Cytometry (1:200-1:400)
    Western Blot (1:500-1:2000)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In PBS (0.05% 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 (Transfected lysate)
  • Western Blot (Transfected lysate)
  • Western Blot analysis of Lane 1: HEK293 and Lane 2: THBD-hIgGFc transfected HEK293 cell lysates with THBD monoclonal antibody, clone 2C6C3 (Cat # MAB21380).
  • Enzyme-linked Immunoabsorbent Assay
  • Enzyme-linked Immunoabsorbent Assay
  • ELISA analysis with THBD monoclonal antibody, clone 2C6C3 (Cat # MAB21380).
  • Flow Cytometry
  • Flow Cytometry
  • Flow cytometric analysis of HL-60 cells with THBD monoclonal antibody, clone 2C6C3 (Cat # MAB21380) (Green). Red: Negative Control.
  • Application Image
  • Western Blot (Transfected lysate)
  • Western Blot (Transfected lysate)
  • enlarge
  • Enzyme-linked Immunoabsorbent Assay
  • Enzyme-linked Immunoabsorbent Assay
  • enlarge
  • Gene Information
  • Entrez GeneID:
  • 7056
  • Gene Name:
  • THBD
  • Gene Alias:
  • CD141,THRM,TM
  • Gene Description:
  • thrombomodulin
  • Gene Summary:
  • The protein encoded by this intronless gene is an endothelial-specific type I membrane receptor that binds thrombin. This binding results in the activation of protein C, which degrades clotting factors Va and VIIIa and reduces the amount of thrombin generated. Mutations in this gene are a cause of thromboembolic disease, also known as inherited thrombophilia. [provided by RefSeq
  • Other Designations:
  • CD141 antigen,OTTHUMP00000030415,fetomodulin
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