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WB analysis of HeLa nuclear lysate using GTX88791 SENP6 antibody, Internal. Dilution : 0.5microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of HeLa nuclear lysate using GTX88791 SENP6 antibody, Internal. Dilution : 0.5microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of HeLa nuclear lysate using GTX88791 SENP6 antibody, Internal. Dilution : 0.5microg/ml Loading : 35microg protein in RIPA buffer

SENP6 antibody, Internal

GTX88791
GeneTex
ApplicationsWestern Blot
Product group Antibodies
ReactivityHuman
TargetSENP6
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Overview

  • Supplier
    GeneTex
  • Product Name
    SENP6 antibody, Internal
  • Delivery Days Customer
    9
  • Antibody Specificity
    This antibody is expected to recognise both reported isoforms (NP_001093879.1; NP_056386.2).
  • Application Supplier Note
    WB: 0.5-1.5microg/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 ID26054
  • Target name
    SENP6
  • Target description
    SUMO specific peptidase 6
  • Target synonyms
    2810017C20Rik; sentrin/SUMO-specific protease SENP6; sentrin-specific protease 6; SSP1; SUMO1/sentrin specific peptidase 6; SUMO1/sentrin specific protease 6; SUMO-1-specific protease 1; SUSP1
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDQ9GZR1
  • Protein Name
    Sentrin-specific protease 6
  • Scientific Description
    Ubiquitin-like molecules (UBLs), such as SUMO1 (UBL1; MIM 601912), are structurally related to ubiquitin (MIM 191339) and can be ligated to target proteins in a similar manner as ubiquitin. However, covalent attachment of UBLs does not result in degradation of the modified proteins. SUMO1 modification is implicated in the targeting of RANGAP1 (MIM 602362) to the nuclear pore complex, as well as in stabilization of I-kappa-B-alpha (NFKBIA; MIM 164008) from degradation by the 26S proteasome. Like ubiquitin, UBLs are synthesized as precursor proteins, with 1 or more amino acids following the C-terminal glycine-glycine residues of the mature UBL protein. Thus, the tail sequences of the UBL precursors need to be removed by UBL-specific proteases, such as SENP6, prior to their conjugation to target proteins (Kim et al., 2000 [PubMed 10799485]). SENPs also display isopeptidase activity for deconjugation of SUMO-conjugated substrates (Lima and Reverter, 2008 [PubMed 18799455]).[supplied by OMIM, Jun 2009]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203