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The image on the left is immunohistochemistry of paraffin-embedded Human liver cancer tissue using CSB-PA172691(CFAP45 Antibody) at dilution 1/25, 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-PA172691(CFAP45 Antibody) at dilution 1/25, 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-PA172691(CFAP45 Antibody) at dilution 1/25, on the right is treated with synthetic peptide. (Original magnification: x200)

CFAP45 Antibody

CSB-PA172691
Cusabio
ApplicationsELISA, ImmunoHistoChemistry
Product group Antibodies
ReactivityHuman
TargetCFAP45
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Overview

  • Supplier
    Cusabio
  • Product Name
    CFAP45 Antibody
  • Delivery Days Customer
    20
  • Applications
    ELISA, ImmunoHistoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID25790
  • Target name
    CFAP45
  • Target description
    cilia and flagella associated protein 45
  • Target synonyms
    CCDC19; cilia- and flagella-associated protein 45; coiled-coil domain containing 19; coiled-coil domain-containing protein 19, mitochondrial; nasopharyngeal epithelium specific protein 1 (NESG1); nasopharyngeal epithelium-specific protein 1; NESG1; protein CFAP45, mitochondrial
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ9UL16
  • Protein Name
    Cilia- and flagella-associated protein 45
  • Scientific Description
    CCDC19 is a 466 amino acid protein encoded by a gene mapping to human chromosome 1. Chromosome 1 is the largest human chromosome, spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1 and, considering the great number of genes, there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes Lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1.
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C
  • UNSPSC
    41116161

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