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Recombinant Human Mesothelin (MSLN), Truncated,Biotinylated

ACP00934

Number
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Specifications


Cat.No ACP00934 Target NameMSLN
FormLiquid or Lyophilized powderExpression SystemMammalian cell
Expression Range296-580aaMol Weight61.4 kDa
Protein LengthPartial of Isoform 3PurityGreater than 90% as determined by 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 IDQ13421
Background Information
  • Uniprot Id

    Q13421

  • Target Species

    Human

  • Target Name

    MSLN

  • Target Full Name

    Mesothelin

  • Target Function

    Membrane-anchored forms may play a role in cellular adhesion.; Megakaryocyte-potentiating factor (MPF) potentiates megakaryocyte colony formation in vitro.

  • Target Involvement

    Antibodies against MSLN are detected in patients with mesothelioma and ovarian cancer.

  • Target Subcellular Location

    Cell membrane; Lipid-anchor, GPI-anchor. Golgi apparatus.; [Megakaryocyte-potentiating factor]: Secreted.; [Isoform 3]: Secreted.

  • Target Protein Families

    Mesothelin family

  • Target Tissue Specificity

    Expressed in lung. Expressed at low levels in heart, placenta and kidney. Expressed in mesothelial cells. Highly expressed in mesotheliomas, ovarian cancers, and some squamous cell carcinomas (at protein level).

  • Target Research Area

    Cancer

  • Target Synonyms

    MPF; SMRP; Mesothelin

  • Target Background

    This gene encodes a preproprotein that is proteolytically processed to generate two protein products, megakaryocyte potentiating factor and mesothelin. Megakaryocyte potentiating factor functions as a cytokine that can stimulate colony formation of bone marrow megakaryocytes. Mesothelin is a glycosylphosphatidylinositol-anchored cell-surface protein that may function as a cell adhesion protein. This protein is overexpressed in epithelial mesotheliomas, ovarian cancers and in specific squamous cell carcinomas. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed.

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