XRCC4 Polyclonal Antibody, 100ul Metabolic enzymes sensory ataxic neuropathy dysarthria and

sensory ataxic neuropathy dysarthria and ophthalmoparesis (SANDO)

a unique amino acid formed by the posttranslational modification of only one protein

Belongs to the phospholipase D family

a neurodegenerative disorder classified as a polyglutamine disease

XRCC4 Polyclonal Antibody, 100ul Metabolic enzymes sensory ataxic neuropathy dysarthria andDNA repair protein XRCC4 encoded by XRCC4 functions together with DNA ligase IV and the DNA dependent protein kinase in the repair of DNA double strand breaks. This protein plays a role in both non homologous end joining and the completion of V(D)J recombination. Mutations in this gene can cause short stature, microcephaly, and endocrine dysfunction (SSMED). Alternative splicing generates several transcript variants.