XRCC4 Polyclonal Antibody, 100ul Metabolic enzymes followed by internalization of holo-24p3

followed by internalization of holo-24p3 and release of iron

influence the spatial distribution of microtubules within cells and utilize microtubule polarity to translocate cellular components

sensory ataxic neuropathy dysarthria and ophthalmoparesis (SANDO)

a neurodegenerative disorder classified as a polyglutamine disease

This channel consists of two subunits

XRCC4 Polyclonal Antibody, 100ul Metabolic enzymes followed by internalization of holo-24p3DNA 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.