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WB analysis of mouse lung tissue lysate using GTX54694 SFTPC antibody. Dilution : 1:1000 Loading : 25microg per lane
WB analysis of mouse lung tissue lysate using GTX54694 SFTPC antibody. Dilution : 1:1000 Loading : 25microg per lane
WB analysis of mouse lung tissue lysate using GTX54694 SFTPC antibody. Dilution : 1:1000 Loading : 25microg per lane

SFTPC antibody

GTX54694
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetSFTPC
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Overview

  • Supplier
    GeneTex
  • Product Name
    SFTPC antibody
  • Delivery Days Customer
    7
  • Application Supplier Note
    WB: 1:500 - 1:2000. IHC-P: 1:50 - 1:200. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID6440
  • Target name
    SFTPC
  • Target description
    surfactant protein C
  • Target synonyms
    BRICD6; BRICHOS domain containing 6; PSP-C; pulmonary surfactant apoprotein-2 SP-C; pulmonary surfactant-associated protein C; pulmonary surfactant-associated proteolipid SPL(Val); SFTP2; SMDP2; SP5; SP-C
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP11686
  • Protein Name
    Pulmonary surfactant-associated protein C
  • Scientific Description
    This gene encodes the pulmonary-associated surfactant protein C (SPC), an extremely hydrophobic surfactant protein essential for lung function and homeostasis after birth. Pulmonary surfactant is a surface-active lipoprotein complex composed of 90% lipids and 10% proteins which include plasma proteins and apolipoproteins SPA, SPB, SPC and SPD. The surfactant is secreted by the alveolar cells of the lung and maintains the stability of pulmonary tissue by reducing the surface tension of fluids that coat the lung. Multiple mutations in this gene have been identified, which cause pulmonary surfactant metabolism dysfunction type 2, also called pulmonary alveolar proteinosis due to surfactant protein C deficiency, and are associated with interstitial lung disease in older infants, children, and adults. Alternatively spliced transcript variants encoding different protein isoforms have been identified.[provided by RefSeq, Feb 2010]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • Abnormal Fetal Lung of Hoxa1(-/-) Piglets Is Rescued by Maternal Feeding with All-Trans Retinoic Acid.
    Read more
  • Ammonia exposure causes lung injuries and disturbs pulmonary circadian clock gene network in a pig study. Wang X et al., 2020 Dec 1, Ecotoxicol Environ Saf
    Read more
  • Enterovirus 71 targets the cardiopulmonary system in a robust oral infection mouse model. Chang CS et al., 2019 Jul 31, Sci Rep
    Read more

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