• Product NameRecombinant Human NIPA1
• Brief DescriptionRecombinant Protein
• Immunogen DescriptionFull length fusion protein
• Target Namenon imprinted in Prader-Willi/Angelman syndrome 1
• Alternative Names    FSP3; SPG6
• Accession No. Swissprot:Q7RTP0
  Gene Accession:BC025678
• UniprotQ7RTP0
• Gene ID123606;
• Storage -20~-80˚C, pH 7.6 PBS

This gene encodes a magnesium transporter that associates with early endosomes and the cell surface in a variety of neuronal and epithelial cells. This protein may play a role in nervous system development and maintenance. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene have been associated with autosomal dominant spastic paraplegia 6.

Note: For in vitro research use only, not for diagnostic or therapeutic use. This product is not a medical device.

• Flow Cytometry (FCM) General Protocol
• Immunofluorescence(IC)
• Immunohistochemistry(Polymer)
• Western Blotting