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Recombinant Human Gelsolin (GSN), E.coli

ACP09247

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP09247 Target NameGSN
Target SynonymsActin depolymerizing factor; Actin-depolymerizing factor; ADF; AGEL; Brevin; DKFZp313L0718; GELS_HUMAN; Gelsolin; GsnFormLiquid or Lyophilized powder
Expression SystemE.coliExpression Range28-782aa
Protein LengthFull Length of Mature ProteinPurity>85% (SDS-PAGE)
Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDP06396
Background Information
  • Uniprot Id

    P06396

  • Target Species

    Human

  • Target Name

    GSN

  • Target Full Name

    Gelsolin

  • Target Function

    Calcium-regulated, actin-modulating protein that binds to the plus (or barbed) ends of actin monomers or filaments, preventing monomer exchange (end-blocking or capping). It can promote the assembly of monomers into filaments (nucleation) as well as sever filaments already formed. Plays a role in ciliogenesis.

  • Target Involvement

    Amyloidosis 5 (AMYL5)

  • Target Subcellular Location

    [Isoform 2]: Cytoplasm, cytoskeleton.; [Isoform 1]: Secreted.

  • Target Protein Families

    Villin/gelsolin family

  • Target Tissue Specificity

    Phagocytic cells, platelets, fibroblasts, nonmuscle cells, smooth and skeletal muscle cells.

  • Target Research Area

    Signal Transduction

  • Target Synonyms

    Actin depolymerizing factor; Actin-depolymerizing factor; ADF; AGEL; Brevin; DKFZp313L0718; GELS_HUMAN; Gelsolin; Gsn

  • Target Background

    The protein encoded by this gene binds to the "plus" ends of actin monomers and filaments to prevent monomer exchange. The encoded calcium-regulated protein functions in both assembly and disassembly of actin filaments. Defects in this gene are a cause of familial amyloidosis Finnish type (FAF). Multiple transcript variants encoding several different isoforms have been found for this gene.

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