Bio-Connect

Anti-Phospho-SHP2 (Y542) Antibody [SN61-01]

ET1611-22
HUABIO
ApplicationsImmunoPrecipitation, Western Blot
Product group Antibodies
ReactivityMouse
TargetPTPN11
100 ul
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Overview

  • Supplier
    HUABIO
  • Product Name
    Anti-Phospho-SHP2 (Y542) Antibody [SN61-01]
  • Delivery Days Customer
    7
  • Applications
    ImmunoPrecipitation, Western Blot
  • Applications Supplier
    WB,IF-Cell,IP
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    SN61-01
  • 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 IDP35235
  • Protein Name
    Tyrosine-protein phosphatase non-receptor type 11
  • Scientific Description
    Tyrosine-protein phosphatase non-receptor type 11 (PTPN11) also known as protein-tyrosine phosphatase 1D (PTP-1D), Src homology region 2 domain-containing phosphatase-2 (SHP-2), or protein-tyrosine phosphatase 2C (PTP-2C) is an enzyme that in humans is encoded by the PTPN11 gene. PTPN11 is a protein tyrosine phosphatase (PTP) Shp2. PTPN11 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.
  • Reactivity
    Mouse
  • Reactivity Supplier
    Mouse
  • Reactivity Supplier Note
    Human
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    41116161