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Recombinant Human Collagen alpha-1 (VI) chain (COL6A1), Truncated

ACP24206

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP24206 Target NameCOL6A1
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 IDP12109
Background Information
  • Uniprot Id

    P12109

  • Target Species

    Human

  • Target Name

    COL6A1

  • Target Full Name

    Collagen alpha-1(VI) chain

  • Target Function

    Collagen VI acts as a cell-binding protein.

  • Target Involvement

    Bethlem myopathy 1 (BTHLM1); Ullrich congenital muscular dystrophy 1 (UCMD1)

  • Target Subcellular Location

    Secreted, extracellular space, extracellular matrix.

  • Target Protein Families

    Type VI collagen family

  • Target Synonyms

    Alpha 1 (VI) chain (61 AA); CO6A1_HUMAN; COL6A1; COL6A2; COL6A3; collagen 6; Collagen alpha 2(VI) chain; Collagen alpha 3(VI) chain; Collagen alpha-1(VI) chain; collagen six; Collagen type VI alpha 1; Collagen type VI alpha 2; Collagen type VI alpha 3; Collagen VI alpha 1 polypeptide; Collagen VI alpha 2 polypeptide; Collagen VI alpha 3 polypeptide; CollagenVI; Human mRNA for collagen VI alpha 2 C terminal globular domain; OPLL; PP3610

  • Target Background

    The collagens are a superfamily of proteins that play a role in maintaining the integrity of various tissues. Collagens are extracellular matrix proteins and have a triple-helical domain as their common structural element. Collagen VI is a major structural component of microfibrils. The basic structural unit of collagen VI is a heterotrimer of the alpha1(VI), alpha2(VI), and alpha3(VI) chains. The alpha2(VI) and alpha3(VI) chains are encoded by the COL6A2 and COL6A3 genes, respectively. The protein encoded by this gene is the alpha 1 subunit of type VI collagen (alpha1(VI) chain). Mutations in the genes that code for the collagen VI subunits result in the autosomal dominant disorder, Bethlem myopathy.

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