EDN3 polyclonal antibody (A01)

Catalog # H00001908-A01

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Size:50 uL
Price: USD $ 243.00
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  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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Western Blot detection against Immunogen (52.29 KDa) .

  • Specification

    Product Description

    Mouse polyclonal antibody raised against a full-length recombinant EDN3.

    Immunogen

    EDN3 (AAH08876, 1 a.a. ~ 238 a.a) full-length recombinant protein with GST tag.

    Sequence

    MEPGLWLLFGLTVTSAAGFVPCSQSGDAGRRGVSQAPTAARSEGDCEETVAGPGEETVAGPGEGTVAPTALQGPSPGSPGQEQAAEGAPEHHRSRRCTCFTYKDKECVYYCHLDIIWINTPEQTVPYGLSNYRGSFRGKRSAGPLPGNLQLSHRPHLRCACVGRYDKACLHFCTQTLDVSSNSRTAEKTDKEEEGKVEVKDQQSKQALDLHHPKLMPGSGLALAPSTCPRCLFQEGAP

    Host

    Mouse

    Reactivity

    Human

    Quality Control Testing

    Antibody Reactive Against Recombinant Protein.

    Western Blot detection against Immunogen (52.29 KDa) .

    Storage Buffer

    50 % glycerol

    Storage Instruction

    Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot (Recombinant protein)

    ELISA

  • Gene Info — EDN3

    Entrez GeneID

    1908

    GeneBank Accession#

    BC008876

    Protein Accession#

    AAH08876

    Gene Name

    EDN3

    Gene Alias

    ET3, MGC15067, MGC61498

    Gene Description

    endothelin 3

    Omim ID

    131242 142623 209880 277580

    Gene Ontology

    Hyperlink

    Gene Summary

    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. Four alternatively spliced transcript variants encoding three distinct isoforms have been observed. [provided by RefSeq

    Other Designations

    OTTHUMP00000031420|truncated endothelin 3

  • Interactome
  • Pathway
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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