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TBL1X (Human) IP-WB Antibody Pair

  • Catalog # : H00006907-PW1
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  • Specification
  • Product Description:
  • This IP-WB antibody pair set comes with one antibody for immunoprecipitation and another to detect the precipitated protein in western blot.
  • Reactivity:
  • Human
  • Quality Control Testing:
  • Immunoprecipitation-Western Blot (IP-WB)

    QC Testing of H00006907-PW1
    Immunoprecipitation of TBL1X transfected lysate using rabbit polyclonal anti-TBL1X and Protein A Magnetic Bead (U0007), and immunoblotted with mouse purified polyclonal anti-TBL1X.
  • Supplied Product:
  • Antibody pair set content:
    1. Antibody pair for IP: rabbit polyclonal anti-TBL1X (300 ul)
    2. Antibody pair for WB: mouse purified polyclonal anti-TBL1X (50 ug)
  • Storage Instruction:
  • Store reagents of the antibody pair set at -20°C or lower. Please aliquot to avoid repeated freeze thaw cycle. Reagents should be returned to -20°C storage immediately after use.
  • Applications
  • Application Image
  • Immunoprecipitation-Western Blot
  • Gene Information
  • Entrez GeneID:
  • 6907
  • Gene Name:
  • TBL1X
  • Gene Alias:
  • EBI,SMAP55,TBL1
  • Gene Description:
  • transducin (beta)-like 1X-linked
  • Gene Summary:
  • The protein encoded by this gene has sequence similarity with members of the WD40 repeat-containing protein family. The WD40 group is a large family of proteins, which appear to have a regulatory function. It is believed that the WD40 repeats mediate protein-protein interactions and members of the family are involved in signal transduction, RNA processing, gene regulation, vesicular trafficking, cytoskeletal assembly and may play a role in the control of cytotypic differentiation. This encoded protein is found as a subunit in corepressor SMRT (silencing mediator for retinoid and thyroid receptors) complex along with histone deacetylase 3 protein. This gene is located adjacent to the ocular albinism gene and it is thought to be involved in the pathogenesis of the ocular albinism with late-onset sensorineural deafness phenotype. Four transcript variants encoding two different isoforms have been found for this gene. This gene is highly similar to the Y chromosome TBL1Y gene. [provided by RefSeq
  • Other Designations:
  • F-box-like/WD repeat-containing protein TBL1X,OTTHUMP00000022880,transducin beta-like 1X
  • Gene Pathway
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