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WB analysis of mouse spinal cord lysate using GTX47596 TREM2 antibody, Internal. Dilution : 1microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of mouse spinal cord lysate using GTX47596 TREM2 antibody, Internal. Dilution : 1microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of mouse spinal cord lysate using GTX47596 TREM2 antibody, Internal. Dilution : 1microg/ml Loading : 35microg protein in RIPA buffer

TREM2 antibody, Internal

GTX47596
GeneTex
ApplicationsWestern Blot
Product group Antibodies
TargetTrem2
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Overview

  • Supplier
    GeneTex
  • Product Name
    TREM2 antibody, Internal
  • Delivery Days Customer
    7
  • Application Supplier Note
    WB: 1-3microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.50 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID83433
  • Target name
    Trem2
  • Target description
    triggering receptor expressed on myeloid cells 2
  • Target synonyms
    Trem; TREM-2; Trem2a; Trem2b; Trem2c; triggering receptor expressed on monocytes 2; triggering receptor expressed on myeloid cells 2; triggering receptor expressed on myeloid cells 2a; triggering receptor expressed on myeloid cells 2b; triggering receptor expressed on myeloid cells 2c
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDQ99NH8
  • Protein Name
    Triggering receptor expressed on myeloid cells 2
  • Scientific Description
    The protein encoded by this gene is part of the immunoglobulin and lectin-like superfamily and functions as part of the innate immune system. This gene forms part of a cluster of genes on mouse chromosome 17 thought to be involved in innate immunity. This protein associates with the adaptor protein Dap-12 and recruits several factors, such as kinases and phospholipase C-gamma, to form a receptor signaling complex that activates myeloid cells, including dendritic cells and microglia. In humans homozygous loss-of-function mutations in this gene cause Nasu-Hakola disease and mutations in this gene may be risk factors to the development of Alzheimers disease. In mouse mutations of this gene serve as a pathophysiological model for polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (Nasu-Hakola disease) and for inflammatory bowel disease. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jan 2013]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

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