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WB analysis of RAG2(AA: 350-527)-hIgGFc transfectedHEK293 cell lysate using GTX83284 RAG2 antibody [4D5].
WB analysis of RAG2(AA: 350-527)-hIgGFc transfectedHEK293 cell lysate using GTX83284 RAG2 antibody [4D5].
WB analysis of RAG2(AA: 350-527)-hIgGFc transfectedHEK293 cell lysate using GTX83284 RAG2 antibody [4D5].

RAG2 antibody [4D5]

GTX83284
GeneTex
ApplicationsWestern Blot, ELISA
Product group Antibodies
ReactivityHuman
TargetRAG2
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Overview

  • Supplier
    GeneTex
  • Product Name
    RAG2 antibody [4D5]
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1/500 - 1/2000. ELISA: 1/10000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ELISA
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    4D5
  • Conjugate
    Unconjugated
  • Gene ID5897
  • Target name
    RAG2
  • Target description
    recombination activating 2
  • Target synonyms
    RAG-2; recombination activating gene 2; V(D)J recombination-activating protein 2
  • Host
    Mouse
  • Isotype
    IgG1
  • Protein IDP55895
  • Protein Name
    V(D)J recombination-activating protein 2
  • Scientific Description
    This gene encodes a protein that is involved in the initiation of V(D)J recombination during B and T cell development. This protein forms a complex with the product of the adjacent recombination activating gene 1, and this complex can form double-strand breaks by cleaving DNA at conserved recombination signal sequences. The recombination activating gene 1 component is thought to contain most of the catalytic activity, while the N-terminal of the recombination activating gene 2 component is thought to form a six-bladed propeller in the active core that serves as a binding scaffold for the tight association of the complex with DNA. A C-terminal plant homeodomain finger-like motif in this protein is necessary for interactions with chromatin components, specifically with histone H3 that is trimethylated at lysine 4. Mutations in this gene cause Omenn syndrome, a form of severe combined immunodeficiency associated with autoimmune-like symptoms. [provided by RefSeq, Jul 2008]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203