Overview

  • Product nameAnti-SH3D20 antibody
    See all SH3D20 primary antibodies
  • Description
    Rabbit polyclonal to SH3D20
  • Tested applicationsSuitable for: WBmore details
  • Species reactivity
    Reacts with: Human
  • Immunogen

    Synthetic peptide conjugated to KLH, corresponding to a region within internal sequence amino acids 197-226 of Human SH3D20 (NP_954976.1, NP_777579.2).

  • Positive control
    • A549 cell line lysates.

Properties

Applications

Our Abpromise guarantee covers the use of ab112898 in the following tested applications.

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

Application Abreviews Notes
WB 1/100 - 1/500. Predicted molecular weight: 98 kDa.

Target

  • FunctionRho GTPase-activating protein which may be involved in clathrin-mediated endocytosis. GTPase activators for the Rho-type GTPases act by converting them to an inactive GDP-bound state. Has activity toward CDC42 and RAC1.
  • Tissue specificityExpressed in germinal center B-cell, spleen, chronic lymphocytic leukemia, pancreatic cancer and lung cancer.
  • Sequence similaritiesContains 1 PH domain.
    Contains 1 Rho-GAP domain.
    Contains 1 SH3 domain.
    Contains 3 WW domains.
  • Cellular localizationCytoplasm. Membrane.
  • Information by UniProt
  • Database links
  • Alternative names
    • ARHGAP27 antibody
    • CAMGAP1 antibody
    • CIN85-associated multi-domain-containing Rho GTPase-activating protein 1 antibody
    • PP905 antibody
    • RHG27_HUMAN antibody
    • Rho GTPase-activating protein 27 antibody
    • Rho-type GTPase-activating protein 27 antibody
    • SH3 domain containing 20 antibody
    • SH3 domain containing protein 20 antibody
    • SH3D20 antibody
    • SH3P20 antibody
    see all

Anti-SH3D20 antibody images

  • Anti-SH3D20 antibody (ab112898) at 1/100 dilution + A549 cell line lysates at 35 µg

    Predicted band size : 98 kDa

References for Anti-SH3D20 antibody (ab112898)

ab112898 has not yet been referenced specifically in any publications.

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