Overview

Properties

Applications

Our Abpromise guarantee covers the use of ab87877 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Notes
Sandwich ELISA Use a concentration of 1 µg/ml. Can be paired for Sandwich ELISA with Rabbit polyclonal to Angiopoietin 4 (ab93657). For sandwich ELISA, use this antibody as Capture at 1 µg/ml with ab93657 as Detection
WB 1/1000. Predicted molecular weight: 57 kDa.
IHC-P 1/250.
ICC 1/400.

Target

  • FunctionBinds to tyrosine-protein kinase receptor TIE2 and activates it.
  • Tissue specificityHighly expressed in the lung with much lower levels found in other tissues.
  • Sequence similaritiesContains 1 fibrinogen C-terminal domain.
  • Cellular localizationSecreted.
  • Target information above from: UniProt accession Q9Y264 The UniProt Consortium
    The Universal Protein Resource (UniProt) in 2010
    Nucleic Acids Res. 38:D142-D148 (2010) .

    Information by UniProt
  • Database links
  • Alternative names
    • AGP4 antibody
    • ANG-3 antibody
    • ANG-4 antibody
    • ANG3 antibody
    • ANG4 antibody
    • Angiopoietin 3 antibody
    • Angiopoietin 4 antibody
    • Angiopoietin-3 antibody
    • Angiopoietin-4 antibody
    • ANGP4_HUMAN antibody
    • ANGPT4 antibody
    • dJ824F16.2 (angiopoietin 4) antibody
    • MGC138181 antibody
    • MGC138183 antibody
    • OTTHUMP00000029947 antibody
    see all

Anti-Angiopoietin 4 antibody images

  • Standard Curve for Angiopoietin 4 dilution range 1pg/ml to 1ug/ml using Capture Antibody Goat polyclonal to Angiopoietin 4 (ab87877) at 1ug/ml and Detector Antibody Rabbit polyclonal to Angiopoietin 4 (ab93657) at 0.5ug/ml
  • Immunohistochemistry on paraffin sections of human lung using ab87877 at 1/250 dilution.
  • Immunohistochemistry on paraffin sections of human liver using ab87877 at 1/250 dilution.

Protocols

References for Anti-Angiopoietin 4 antibody (ab87877)

ab87877 has not yet been referenced specifically in any publications.

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