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Last updated: 2017/1/15

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NIPA1 rabbit monoclonal antibody

  • Catalog # : H00123606-K
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  • Specification
  • Product Description:
  • Rabbit monoclonal antibody raised against a human NIPA1 peptide using ARM Technology.
  • Immunogen:
  • A synthetic peptide of human NIPA1 is used for rabbit immunization.
    Customer or Abnova will decide on the preferred peptide sequence.
  • Host:
  • Rabbit
  • Reactivity:
  • Human
  • Purification:
  • Protein A
  • Isotype:
  • IgG
  • Quality Control Testing:
  • Antibody reactive against human NIPA1 peptide by ELISA and mammalian transfected lysate by Western Blot.
  • Storage Buffer:
  • In 1x PBS, pH 7.4
  • Storage Instruction:
  • Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
  • Note:
  • 1. Customer may provide cell or tissue lysate for antibody screening.
    2. Rabbit monoclonal antibody generated by ARM technology is amenable to antibody engineering including F(ab)2, IgG, scFv and different Fc and non-Fc conjugates per customer request.
  • Library Construction:
  • Non-fusion antibody library from rabbit spleen (ARM Technology).
  • Expression:
  • Overexpression vector and transfection into 293H cell line.
  • Deliverable:
  • Up to three rabbit IgG clones of 1 mg each will be delivered to customer.
  • Applications
  • ELISA
  • Application Image
  • Western Blot (Transfected lysate)
  • ELISA
  • Gene Information
  • GeneBank Accession#:
  • NIPA1
  • Gene Name:
  • NIPA1
  • Gene Alias:
  • FSP3,MGC102724,MGC35570,SPG6
  • Gene Description:
  • non imprinted in Prader-Willi/Angelman syndrome 1
  • Gene Summary:
  • 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. [provided by RefSeq
  • Other Designations:
  • non-imprinted in Prader-Willi/Angelman syndrome 1,spastic paraplegia 6 (autosomal dominant)
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