FLT4 monoclonal antibody, clone KLT9

Catalog # MAB22784

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Size:1 mL
Price: USD $ 747.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Application

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)

Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human placenta.

  • Specification

    Product Description

    Mouse monoclonal antibody raised against partial recombinant human FLT4.

    Immunogen

    Recombinant protein corresponding to 227 amino acids region of the external domain of the human FLT4.

    Host

    Mouse

    Reactivity

    Human

    Specificity

    Human vascular endothelial growth factor receptor-3 (VEGFR-3).

    Form

    Liquid

    Isotype

    IgG2b, kappa

    Recommend Usage

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (1:50-1:100, 60 minutes primary antibody incubation at 25°C)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In tissue culture supernatant (15 mM sodium azide).

    Storage Instruction

    Store at 4°C. Prepare working dilutions on the day of use.

    Note

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Recommended positive control for immunohistochemistry is placenta.

  • Applications

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)

    Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human placenta.
  • Gene Info — FLT4

    Entrez GeneID

    2324

    Gene Name

    FLT4

    Gene Alias

    FLT41, LMPH1A, PCL, VEGFR3

    Gene Description

    fms-related tyrosine kinase 4

    Omim ID

    136352 153100 602089

    Gene Ontology

    Hyperlink

    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

  • Interactome
  • Pathway
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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