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RAG2

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.
Protein class

Disease related genes, Human disease related genes

Predicted location

Intracellular

Single cell type specificity

Group enriched (Excitatory neurons, Oligodendrocyte precursor cells, Early spermatids, Inhibitory neurons, Spermatocytes, Oligodendrocytes, Astrocytes)

Immune cell specificity

Not detected in immune cells

Cell line specificity

Cell line enhanced (JURKAT, MOLT-4, REH)

Interaction

Component of the RAG complex composed of core components RAG1 and RAG2, and associated component HMGB1 or HMGB2.

Molecular function

Chromatin regulator

More Types Infomation

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For Research Use Only. Not For Clinical Use.

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