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The image on the left is immunohistochemistry of paraffin-embedded Human liver cancer tissue using CSB-PA136380(IMPAD1 Antibody) at dilution 1/20, on the right is treated with synthetic peptide. (Original magnification: x200)
The image on the left is immunohistochemistry of paraffin-embedded Human liver cancer tissue using CSB-PA136380(IMPAD1 Antibody) at dilution 1/20, on the right is treated with synthetic peptide. (Original magnification: x200)
The image on the left is immunohistochemistry of paraffin-embedded Human liver cancer tissue using CSB-PA136380(IMPAD1 Antibody) at dilution 1/20, on the right is treated with synthetic peptide. (Original magnification: x200)

IMPAD1 Antibody

CSB-PA136380
Cusabio
ApplicationsELISA, ImmunoHistoChemistry
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetBPNT2
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Overview

  • Supplier
    Cusabio
  • Product Name
    IMPAD1 Antibody
  • Delivery Days Customer
    20
  • Applications
    ELISA, ImmunoHistoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID54928
  • Target name
    BPNT2
  • Target description
    3'(2'), 5'-bisphosphate nucleotidase 2
  • Target synonyms
    GPAPP, IMP 3, IMP-3, IMPA3, IMPAD1, Golgi-resident adenosine 3',5'-bisphosphate 3'-phosphatase, Golgi 3-prime phosphoadenosine 5-prime phosphate 3-prime phosphatase, IMPase 3, golgi-resident PAP phosphatase, golgi-resident nucleotide phosphatase, inositol monophosphatase domain containing 1, inositol monophosphatase domain-containing protein 1, inositol-1(or 4)-monophosphatase 3, myo-inositol monophosphatase A3, phosphoadenosine phosphate 3'-nucleotidase
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ9NX62
  • Protein Name
    Golgi-resident adenosine 3',5'-bisphosphate 3'-phosphatase
  • Scientific Description
    This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.
  • Reactivity
    Human, Mouse, Rat
  • Storage Instruction
    -20°C or -80°C
  • UNSPSC
    41116161