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WB analysis of A431 cell lysate using GTX88931 TMPRSS3 antibody, Internal. Dilution : 0.1microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of A431 cell lysate using GTX88931 TMPRSS3 antibody, Internal. Dilution : 0.1microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of A431 cell lysate using GTX88931 TMPRSS3 antibody, Internal. Dilution : 0.1microg/ml Loading : 35microg protein in RIPA buffer

TMPRSS3 antibody, Internal

GTX88931
GeneTex
ApplicationsWestern Blot
Product group Antibodies
ReactivityHuman
TargetTMPRSS3
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Overview

  • Supplier
    GeneTex
  • Product Name
    TMPRSS3 antibody, Internal
  • Delivery Days Customer
    7
  • Antibody Specificity
    This antibody is expected to recognise all four reported isoforms (NP_076927.1; NP_115777.1; NP_115780.1; NP_115781.1)
  • Application Supplier Note
    WB: 0.1-0.3microg/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 ID64699
  • Target name
    TMPRSS3
  • Target description
    transmembrane serine protease 3
  • Target synonyms
    DFNB10; DFNB8; ECHOS1; serine protease TADG-12; TADG12; transmembrane protease serine 3; transmembrane protease, serine 3; tumor-associated differentially-expressed gene 12 protein
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDP57727
  • Protein Name
    Transmembrane protease serine 3
  • Scientific Description
    This gene encodes a protein that belongs to the serine protease family. The encoded protein contains a serine protease domain, a transmembrane domain, an LDL receptor-like domain, and a scavenger receptor cysteine-rich domain. Serine proteases are known to be involved in a variety of biological processes, whose malfunction often leads to human diseases and disorders. This gene was identified by its association with both congenital and childhood onset autosomal recessive deafness. This gene is expressed in fetal cochlea and many other tissues, and is thought to be involved in the development and maintenance of the inner ear or the contents of the perilymph and endolymph. This gene was also identified as a tumor-associated gene that is overexpressed in ovarian tumors. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jan 2012]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203