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WB analysis of mouse skeletal muscle tissue lysate using GTX31745 SHP2 antibody. Working concentration : (A) 0.5 and (B) 1 microg/ml
WB analysis of mouse skeletal muscle tissue lysate using GTX31745 SHP2 antibody. Working concentration : (A) 0.5 and (B) 1 microg/ml
WB analysis of mouse skeletal muscle tissue lysate using GTX31745 SHP2 antibody. Working concentration : (A) 0.5 and (B) 1 microg/ml

SHP2 antibody

GTX31745
GeneTex
ApplicationsWestern Blot, ELISA, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetPTPN11
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Overview

  • Supplier
    GeneTex
  • Product Name
    SHP2 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 0.5 - 1 microg/mL. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ELISA, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID5781
  • Target name
    PTPN11
  • Target description
    protein tyrosine phosphatase non-receptor type 11
  • Target synonyms
    BPTP3, CFC, JMML, METCDS, NS1, PTP-1D, PTP2C, SH-PTP2, SH-PTP3, SHP2, tyrosine-protein phosphatase non-receptor type 11, SH2 domain-containing protein tyrosine phosphatase 2, protein-tyrosine phosphatase 1D, protein-tyrosine phosphatase 2C
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ06124
  • Protein Name
    Tyrosine-protein phosphatase non-receptor type 11
  • Scientific Description
    The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP contains two tandem Src homology-2 domains, which function as phospho-tyrosine binding domains and mediate the interaction of this PTP with its substrates. This PTP is widely expressed in most tissues and plays a regulatory role in various cell signaling events that are important for a diversity of cell functions, such as mitogenic activation, metabolic control, transcription regulation, and cell migration. Mutations in this gene are a cause of Noonan syndrome as well as acute myeloid leukemia. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203