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The image on the left is immunohistochemistry of paraffin-embedded Human esophagus cancer tissue using CSB-PA178293(TRIM74 Antibody) at dilution 1/45, on the right is treated with fusion protein. (Original magnification: x200)
The image on the left is immunohistochemistry of paraffin-embedded Human esophagus cancer tissue using CSB-PA178293(TRIM74 Antibody) at dilution 1/45, on the right is treated with fusion protein. (Original magnification: x200)
The image on the left is immunohistochemistry of paraffin-embedded Human esophagus cancer tissue using CSB-PA178293(TRIM74 Antibody) at dilution 1/45, on the right is treated with fusion protein. (Original magnification: x200)

TRIM74 Antibody

CSB-PA178293
Cusabio
ApplicationsELISA, ImmunoHistoChemistry
Product group Antibodies
ReactivityHuman
TargetTRIM74
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Overview

  • Supplier
    Cusabio
  • Product Name
    TRIM74 Antibody
  • Delivery Days Customer
    20
  • Applications
    ELISA, ImmunoHistoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID378108
  • Target name
    TRIM74
  • Target description
    tripartite motif containing 74
  • Target synonyms
    TRIM50C, tripartite motif-containing protein 74, tripartite motif-containing 50C, tripartite motif-containing protein 50C
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ86UV6
  • Protein Name
    Tripartite motif-containing protein 74
  • Scientific Description
    TRIM 74 (Tripartite motif-containing protein 74) is a possible protein coding regions found at gene location 7q11.23. Tripartite motif (TRIM) proteins play important roles in a variety of cellular functions including cell proliferation, differentiation, development, oncogenesis, and apoptosis. TRIM gene expression analysis in primary human immune cells seem to suggest the involvement of TRIM proteins in also regulating host antiviral activities. The gene encoding TRIM 74 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C
  • UNSPSC
    41116161