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Recombinant Human Fibroblast growth factor 17 (FGF17)

ACP20769

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP20769 Target NameFGF17
Target SynonymsFGF 13; FGF 17; FGF-17; FGF13; Fgf17; FGF17_HUMAN; Fibroblast growth factor 17; HH20FormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Expression Range23-216
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 IDO60258
Background Information
  • Uniprot Id

    O60258

  • Target Species

    Human

  • Target Name

    FGF17

  • Target Full Name

    Fibroblast growth factor 17

  • Target Function

    Plays an important role in the regulation of embryonic development and as signaling molecule in the induction and patterning of the embryonic brain. Required for normal brain development.

  • Target Involvement

    Hypogonadotropic hypogonadism 20 with or without anosmia (HH20)

  • Target Subcellular Location

    Secreted.

  • Target Protein Families

    Heparin-binding growth factors family

  • Target Tissue Specificity

    Preferentially expressed in the embryonic brain.

  • Target Synonyms

    FGF 13; FGF 17; FGF-17; FGF13; Fgf17; FGF17_HUMAN; Fibroblast growth factor 17; HH20

  • Target Background

    This gene encodes a member of the fibroblast growth factor (FGF) family. Member of the FGF family possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes including embryonic development cell growth, morphogenesis, tissue repair, tumor growth and invasion. This protein is expressed during embryogenesis and in the adult cerebellum and cortex and may be essential for vascular growth and normal brain development. Mutations in this gene are the cause of hypogonadotropic hypogonadism 20 with or without anosmia. Alternate splicing results in multiple transcript variants.

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