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RAS antibody [F132-62]

GTX16907
GeneTex
ApplicationsImmunoFluorescence, ImmunoPrecipitation, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Frozen, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetKRAS
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Overview

  • Supplier
    GeneTex
  • Product Name
    RAS antibody [F132-62]
  • Delivery Days Customer
    9
  • Application Supplier Note
    For IF: Use at a concentration of 1.5 - 2.5 microg/ml. For IHC-P: Use at a concentration of 4 - 6microg/ml. For IHC-Fr: Use at a concentration of 4 - 6microg/ml. For IP: Use at a concentration of 3 - 5microg/ml. Not suitable for use in Western Blot. Optimal dilutions/concentrations should be determined by the researcher.
  • Applications
    ImmunoFluorescence, ImmunoPrecipitation, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Frozen, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    F132-62
  • Concentration
    0.1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID3845
  • Target name
    KRAS
  • Target description
    KRAS proto-oncogene, GTPase
  • Target synonyms
    cellular c-Ki-ras2 proto-oncogene; cellular transforming proto-oncogene; CFC2; c-Ki-ras; c-Ki-ras2; c-Kirsten-ras protein; 'C-K-RAS; C-K-RAS; GTPase KRas; KI-RAS; Kirsten rat sarcoma viral oncogene homolog; Kirsten rat sarcoma viral proto-oncogene; K-Ras; K-Ras 2; K-ras p21 protein; KRAS1; KRAS2; K-RAS2A; K-RAS2B; K-RAS4A; K-RAS4B; NS; NS3; OES; oncogene KRAS2; PR310 c-K-ras oncogene; RALD; RASK2; transforming protein p21; v-Ki-ras2 Kirsten rat sarcoma 2 viral oncogene homolog
  • Host
    Mouse
  • Isotype
    IgG2b
  • Scientific Description
    This gene belongs to the Ras oncogene family, whose members are related to the transforming genes of mammalian sarcoma retroviruses. The products encoded by these genes function in signal transduction pathways. These proteins can bind GTP and GDP, and they have intrinsic GTPase activity. This protein undergoes a continuous cycle of de- and re-palmitoylation, which regulates its rapid exchange between the plasma membrane and the Golgi apparatus. Mutations in this gene cause Costello syndrome, a disease characterized by increased growth at the prenatal stage, growth deficiency at the postnatal stage, predisposition to tumor formation, mental retardation, skin and musculoskeletal abnormalities, distinctive facial appearance and cardiovascular abnormalities. Defects in this gene are implicated in a variety of cancers, including bladder cancer, follicular thyroid cancer, and oral squamous cell carcinoma. Multiple transcript variants, which encode different isoforms, have been identified for
  • Storage Instruction
    2°C to 8°C
  • UNSPSC
    12352203

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