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Recombinant Human MAGUK p55 subfamily member 7 (MPP7)

ACP16973

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP16973 Target NameMPP7
Target SynonymsFLJ32798; MAGUK p55 subfamily member 7; Membrane protein palmitoylated 7 MAGUK p55 subfamily member 7; MPP7; MPP7_HUMAN; Palmitoylated membrane protein 7FormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Expression Range1-576
Protein LengthFull length 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 IDQ5T2T1
Background Information
  • Uniprot Id

    Q5T2T1

  • Target Species

    Human

  • Target Name

    MPP7

  • Target Full Name

    MAGUK p55 subfamily member 7

  • Target Function

    Acts as an important adapter that promotes epithelial cell polarity and tight junction formation via its interaction with DLG1. Involved in the assembly of protein complexes at sites of cell-cell contact.

  • Target Subcellular Location

    Membrane; Peripheral membrane protein. Lateral cell membrane; Peripheral membrane protein. Cell junction, tight junction. Cell junction, adherens junction. Cytoplasm, cell cortex. Cytoplasm.

  • Target Protein Families

    MAGUK family

  • Target Synonyms

    FLJ32798; MAGUK p55 subfamily member 7; Membrane protein palmitoylated 7 MAGUK p55 subfamily member 7; MPP7; MPP7_HUMAN; Palmitoylated membrane protein 7

  • Target Background

    The protein encoded by this gene is a member of the p55 Stardust family of membrane-associated guanylate kinase (MAGUK) proteins, which function in the establishment of epithelial cell polarity. This family member forms a complex with the polarity protein DLG1 (discs, large homolog 1) and facilitates epithelial cell polarity and tight junction formation. Polymorphisms in this gene are associated with variations in site-specific bone mineral density (BMD). Alternative splicing results in multiple transcript variants.

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