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Recombinant Human Coactosin-like protein (COTL1)

ACP17859

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP17859 Target NameCOTL1
Target SynonymsCLP; Coactosin like 1; Coactosin-like protein; COTL1; COTL1_HUMAN; FLJ43657; MGC19733FormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Expression Range2-142
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 IDQ14019
Background Information
  • Uniprot Id

    Q14019

  • Target Species

    Human

  • Target Name

    COTL1

  • Target Full Name

    Coactosin-like protein

  • Target Function

    Binds to F-actin in a calcium-independent manner. Has no direct effect on actin depolymerization. Acts as a chaperone for ALOX5 (5LO), influencing both its stability and activity in leukotrienes synthesis.

  • Target Subcellular Location

    Cytoplasm. Cytoplasm, cytoskeleton. Nucleus.

  • Target Protein Families

    Actin-binding proteins ADF family, Coactosin subfamily

  • Target Tissue Specificity

    Widely expressed with highest levels in placenta, lung, kidney and peripheral blood leukocytes and lower levels in brain, liver and pancreas.

  • Target Research Area

    Signal Transduction

  • Target Synonyms

    CLP; Coactosin like 1; Coactosin-like protein; COTL1; COTL1_HUMAN; FLJ43657; MGC19733

  • Target Background

    This gene encodes one of the numerous actin-binding proteins which regulate the actin cytoskeleton. This protein binds F-actin, and also interacts with 5-lipoxygenase, which is the first committed enzyme in leukotriene biosynthesis. Although this gene has been reported to map to chromosome 17 in the Smith-Magenis syndrome region, the best alignments for this gene are to chromosome 16. The Smith-Magenis syndrome region is the site of two related pseudogenes.

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