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Neuroscience Neurology process Growth and Development Neurotrophins

Recombinant Human Neurturin protein (ab9840)

Key features and details

  • Expression system: Escherichia coli
  • Endotoxin level:
  • Suitable for: SDS-PAGE, Functional Studies

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Description

  • Product name

    Recombinant Human Neurturin protein
  • Endotoxin level

  • Expression system

    Escherichia coli
  • Protein length

    Full length protein
  • Animal free

    No
  • Nature

    Recombinant
    • Species

      Human
    • Predicted molecular weight

      22 kDa
  • Specifications

    Our Abpromise guarantee covers the use of ab9840 in the following tested applications.

    The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

    • Applications

      SDS-PAGE

      Functional Studies

    • Form

      Lyophilized
    • Additional notes

      Human Neurturin is fully biologically active when compared to standards. Human Neurturin at a concentration of 100ng/ml will support the survival of 65% of newborn rat sympathetic neurons.
    • Concentration information loading...

    Preparation and Storage

    • Stability and Storage

      Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.

    • Reconstitution
      Reconstitute in water to a concentration of 0.1mg/ml

    General Info

    • Alternative names

      • Neurturin
      • Neurturin precursor
      • NRTN
      • NRTN_HUMAN
      • NTN
      • prepro-neurturin
      see all
    • Function

      Supports the survival of sympathetic neurons in culture. May regulate the development and maintenance of the CNS. Might control the size of non-neuronal cell population such as haemopoietic cells.
    • Involvement in disease

      Defects in NRTN are a cause of Hirschsprung disease (HSCR) [MIM:142623]. In association with mutations of RET gene, and possibly with other loci, defects in NRTN are involved in Hirschsprung disease. This genetic disorder of neural crest development is characterized by the absence of intramural ganglion cells in the hindgut, often resulting in intestinal obstruction.
    • Sequence similarities

      Belongs to the TGF-beta family. GDNF subfamily.
    • Cellular localization

      Secreted.
    • Target information above from: UniProt accession Q99748 The UniProt Consortium
      The Universal Protein Resource (UniProt) in 2010
      Nucleic Acids Res. 38:D142-D148 (2010) .

      Information by UniProt

Protocols

To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.

Click here to view the general protocols

Datasheets and documents

    • Datasheet
  • References (0)

    Publishing research using ab9840? Please let us know so that we can cite the reference in this datasheet.

    ab9840 has not yet been referenced specifically in any publications.

    Preparation and Storage

    • Neurturin
    • Neurturin precursor
    • NRTN

    Images

    Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES"
    For licensing inquiries, please contact partnerships@abcam.com

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