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Recombinant Human Endothelin-3 (EDN3)

ACP20416

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP20416 Target NameEDN3
Target SynonymsEDN3; EDN3_HUMAN; Endothelin 3; Endothelin-3; ET 3; ET-3; PPET3; Preproendothelin 3; Preproendothelin-3FormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Expression Range97-117
Protein LengthCytoplasmic DomainPurity>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 IDP14138
Background Information
  • Uniprot Id

    P14138

  • Target Species

    Human

  • Target Name

    EDN3

  • Target Full Name

    Endothelin-3

  • Target Function

    Endothelins are endothelium-derived vasoconstrictor peptides.

  • Target Involvement

    Hirschsprung disease 4 (HSCR4); Congenital central hypoventilation syndrome (CCHS); Waardenburg syndrome 4B (WS4B)

  • Target Subcellular Location

    Secreted.

  • Target Protein Families

    Endothelin/sarafotoxin family

  • Target Tissue Specificity

    Expressed in trophoblasts and placental stem villi vessels, but not in cultured placental smooth muscle cells.

  • Target Research Area

    Cancer

  • Target Synonyms

    EDN3; EDN3_HUMAN; Endothelin 3; Endothelin-3; ET 3; ET-3; PPET3; Preproendothelin 3; Preproendothelin-3

  • Target Background

    The protein encoded by this gene is a member of the endothelin family. Endothelins are endothelium-derived vasoactive peptides involved in a variety of biological functions. The active form of this protein is a 21 amino acid peptide processed from the precursor protein. The active peptide is a ligand for endothelin receptor type B (EDNRB). The interaction of this endothelin with EDNRB is essential for development of neural crest-derived cell lineages, such as melanocytes and enteric neurons. Mutations in this gene and EDNRB have been associated with Hirschsprung disease (HSCR) and Waardenburg syndrome (WS), which are congenital disorders involving neural crest-derived cells. Altered expression of this gene is implicated in tumorigenesis. Alternative splicing results in multiple transcript variants encoding different isoforms.

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