GEN Rabbit Polyclonal Antibody, 50ul Immune Cell Analysis Mutations in this gene cause

Mutations in this gene cause startle disease

May have relatively low activity

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This gene contains a GCG trinucleotide repeat at the 5' end of the coding region

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GEN Rabbit Polyclonal Antibody, 50ul Immune Cell Analysis Mutations in this gene causeThis gene encodes a member of the Rad2 xeroderma pigmentosum group G nuclease family whose members are characterized by N terminal and internal xeroderma pigmentosum group G nuclease domains followed by helix hairpin helix domains and disordered C terminal domains. The protein encoded by this gene is involved in resolution of Holliday junctions which are intermediate four way structures that covalently link DNA during homologous recombination and