RAG2-Polyclonal Antibodies

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RAG2

Qty


Total
$220
Catalog #
A5626
Antibody Type
Polyclonal Antibody
Gene ID
5897
Swiss Prot
P55895
Size
Species
Rabbit
Isotype
IgG
Purity
Affinity purification
Additional Information
ReactivityHuman Mouse Rat
Tested applicationsWB IHC IF
Recommended DilutionWB 1:500 - 1:2000 IHC 1:50 - 1:200 IF 1:50 - 1:200
Calculated MW59kDa
Observed MWRefer to Figures
ImmunogenRecombinant protein of human RAG2
Storage BufferStore at -20℃. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
SynonymRAG-2;
Images
  • A5626: image 1

    Western blot analysis of extracts of various cell lines, using RAG2 antibody.

  • A5626: image 2

    Immunofluorescence analysis of U20S cell using RAG2 antibody. Blue: DAPI for nuclear staining.

  • A5626: image 3

    Immunofluorescence analysis of GFP-RNF168 trangenic U2OS cell using RAG2 antibody. Green:GFP-RNF168 fusion protein expression for DNA damage marker.Blue: DAPI for nuclear staining.RNF168(GFP) can be used to mark cells damaged by UV-A laser for they always gather around DNA damage region.

Background

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.

Protocol

N/A

MSDS
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