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Last updated: 2017/5/28

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FLT4 monoclonal antibody, clone 44CT92.4.4

  • Catalog # : MAB12327
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  • Specification
  • Product Description:
  • Mouse monoclonal antibody raised against partial recombinant human FLT4.
  • Immunogen:
  • Recombinant His fusion protein corresponding to human FLT4.
  • Host:
  • Mouse
  • Reactivity:
  • Human
  • Form:
  • Liquid
  • Purification:
  • Protein G purification
  • Isotype:
  • IgG1, kappa
  • Recommend Usage:
  • Immunohistochemistry (1:10-1:50)
    Western Blot (1:2000)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In PBS (0.09% 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 (Recombinant protein)
  • Western Blot (Recombinant protein)
  • Western blot analysis of FLT4 recombinant protein reacted with FLT4 monoclonal antibody (Cat # MAB12327) at 1:2000 dilution.
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemical staining of formalin-fixed and paraffin-embedded human lung carcinoma tissue reacted with FLT4 monoclonal antibody (Cat # MAB12327) at 1:10-1:50 dilution.
  • Application Image
  • Western Blot (Recombinant protein)
  • Western Blot (Recombinant protein)
  • enlarge
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • enlarge
  • Gene Information
  • Entrez GeneID:
  • 2324
  • Gene Name:
  • FLT4
  • Gene Alias:
  • FLT41,LMPH1A,PCL,VEGFR3
  • Gene Description:
  • fms-related tyrosine kinase 4
  • Gene Summary:
  • This gene encodes a tyrosine kinase receptor for vascular endothelial growth factors C and D. The protein is thought to be involved in lymphangiogenesis and maintenance of the lymphatic endothelium. Mutations in this gene cause hereditary lymphedema type IA. [provided by RefSeq
  • Other Designations:
  • soluble VEGFR3 variant 1,soluble VEGFR3 variant 2,soluble VEGFR3 variant 3,vascular endothelial growth factor receptor 3
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