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Recombinant Human Collagen alpha-1 (IX) chain (COL9A1), Truncated

ACP24052

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP24052 Target NameCOL9A1
Target SynonymsCOL9A1Collagen alpha-1(IX) chainFormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Protein LengthPartial
Purity>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 IDP20849
Background Information
  • Uniprot Id

    P20849

  • Target Species

    Human

  • Target Name

    COL9A1

  • Target Full Name

    Collagen alpha-1(IX) chain

  • Target Function

    Structural component of hyaline cartilage and vitreous of the eye.

  • Target Involvement

    Multiple epiphyseal dysplasia 6 (EDM6); Stickler syndrome 4 (STL4)

  • Target Subcellular Location

    Secreted, extracellular space, extracellular matrix.

  • Target Protein Families

    Fibril-associated collagens with interrupted helices (FACIT) family

  • Target Synonyms

    COL9A1Collagen alpha-1(IX) chain

  • Target Background

    This gene encodes one of the three alpha chains of type IX collagen, which is a minor (5-20%) collagen component of hyaline cartilage. Type IX collagen is usually found in tissues containing type II collagen, a fibrillar collagen. Studies in knockout mice have shown that synthesis of the alpha 1 chain is essential for assembly of type IX collagen molecules, a heterotrimeric molecule, and that lack of type IX collagen is associated with early onset osteoarthritis. Mutations in this gene are associated with osteoarthritis in humans, with multiple epiphyseal dysplasia, 6, a form of chondrodysplasia, and with Stickler syndrome, a disease characterized by ophthalmic, orofacial, articular, and auditory defects. Two transcript variants that encode different isoforms have been identified for this gene.

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