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Recombinant Human Osteopetrosis-associated transmembrane protein 1 (OSTM1), Truncated

ACP15624

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP15624 Target NameOSTM1
FormLyophilized powderExpression SystemCustom Production. Please inquire and provide the desire expression system.
Protein LengthPartialPurity>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 IDQ86WC4
Background Information
  • Uniprot Id

    Q86WC4

  • Target Species

    Human

  • Target Name

    OSTM1

  • Target Full Name

    Osteopetrosis-associated transmembrane protein 1

  • Target Function

    Required for osteoclast and melanocyte maturation and function.

  • Target Involvement

    Osteopetrosis, autosomal recessive 5 (OPTB5)

  • Target Subcellular Location

    Lysosome membrane; Single-pass type I membrane protein. Note=Requires CLCN7 to travel to lysosomes.

  • Target Protein Families

    OSTM1 family

  • Target Synonyms

    Chloride channel 7 beta subunit; GAIP-interacting protein N terminus; GIPN; GL; Grey lethal osteopetrosis; HSPC019; OPTB5; Osteopetrosis-associated transmembrane protein 1; Ostm1; OSTM1_HUMAN; OTTHUMP00000016938; OTTHUMP00000196342

  • Target Background

    This gene encodes a protein that may be involved in the degradation of G proteins via the ubiquitin-dependent proteasome pathway. The encoded protein binds to members of subfamily A of the regulator of the G-protein signaling (RGS) family through an N-terminal leucine-rich region. This protein also has a central RING finger-like domain and E3 ubiquitin ligase activity. This protein is highly conserved from flies to humans. Defects in this gene may cause the autosomal recessive, infantile malignant form of osteopetrosis.

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