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IHC-P analysis of mouse kidney tissue using GTX32148 GLIS2 antibody. Working concentration : 5 microg/ml
IHC-P analysis of mouse kidney tissue using GTX32148 GLIS2 antibody. Working concentration : 5 microg/ml
IHC-P analysis of mouse kidney tissue using GTX32148 GLIS2 antibody. Working concentration : 5 microg/ml

GLIS2 antibody

GTX32148
GeneTex
ApplicationsWestern Blot, ELISA, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetGLIS2
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Overview

  • Supplier
    GeneTex
  • Product Name
    GLIS2 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1 - 2 microg/mL. IHC-P: 5 microg/mL. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ELISA, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID84662
  • Target name
    GLIS2
  • Target description
    GLIS family zinc finger 2
  • Target synonyms
    NKL, NPHP7, zinc finger protein GLIS2, GLI-similar 2, Kruppel-like zinc finger protein GLIS2, nephrocystin-7, neuronal Krueppel-like protein
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ9BZE0
  • Protein Name
    Zinc finger protein GLIS2
  • Scientific Description
    This gene is a member of the GLI-similar zinc finger protein family and encodes a nuclear transcription factor with five C2H2-type zinc finger domains. The protein encoded by this gene is widely expressed at low levels in the neural tube and peripheral nervous system and likely promotes neuronal differentiation. It is abundantly expressed in the kidney and may have a role in the regulation of kidney morphogenesis. p120 regulates the expression level of this protein and induces the cleavage of this proteins C-terminal zinc finger domain. This protein also promotes the nuclear translocation of p120. Mutations in this gene cause nephronophthisis (NPHP), an autosomal recessive kidney disease characterized by tubular basement membrane disruption, interstitial lymphohistiocytic cell infiltration, and development of cysts at the corticomedullary border of the kidneys.[provided by RefSeq, Jan 2010]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203