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Recombinant Human Tribbles homolog 2 (TRIB2)

ACP14166

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP14166 Target NameTRIB2
Target SynonymsC5FW; FLJ57420; GS3955; Hypothetical protein TRB2; TRB-2; TRB2; TRIB 2; TRIB2; TRIB2_HUMAN; Tribbles homolog 2FormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Expression Range1-343
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 IDQ92519
Background Information
  • Uniprot Id

    Q92519

  • Target Species

    Human

  • Target Name

    TRIB2

  • Target Full Name

    Tribbles homolog 2

  • Target Function

    Interacts with MAPK kinases and regulates activation of MAP kinases. Does not display kinase activity.

  • Target Subcellular Location

    Cytoplasm. Cytoplasm, cytoskeleton.

  • Target Protein Families

    Protein kinase superfamily, CAMK Ser/Thr protein kinase family, Tribbles subfamily

  • Target Tissue Specificity

    Highly expressed in peripheral blood leukocytes.

  • Target Synonyms

    C5FW; FLJ57420; GS3955; Hypothetical protein TRB2; TRB-2; TRB2; TRIB 2; TRIB2; TRIB2_HUMAN; Tribbles homolog 2

  • Target Background

    This gene encodes one of three members of the Tribbles family. The Tribbles members share a Trb domain, which is homologous to protein serine-threonine kinases, but lacks the active site lysine and probably lacks a catalytic function. The Tribbles proteins interact and modulate the activity of signal transduction pathways in a number of physiological and pathological processes. This Tribbles member induces apoptosis of cells mainly of the hematopoietic origin. It has been identified as a protein up-regulated by inflammatory stimuli in myeloid (THP-1) cells, and also as an oncogene that inactivates the transcription factor C/EBPalpha (CCAAT/enhancer-binding protein alpha) and causes acute myelogenous leukemia. Alternatively spliced transcript variants have been found for this gene.

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