FYCO1 Polyclonal Antibody, 20ul Cell Culture & Maintenance Interacts with RAD50 during late

Interacts with RAD50 during late S and G2/M phases

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Mutations in DCLRE1C can cause Athabascan-type severe combined immunodeficiency (SCIDA) and Omenn syndrome

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which shows substantial homology to Ca2+/calmodulin-dependent protein kinase

FYCO1 Polyclonal Antibody, 20ul Cell Culture & Maintenance Interacts with RAD50 during lateThis gene encodes a protein that contains a RUN domain, FYVE type zinc finger domain and Golgi dynamics (GOLD) domain. The encoded protein plays a role in microtubule plus end directed transport of autophagic vesicles through interactions with the small GTPase Rab7, phosphatidylinositol 3 phosphate (PI3P) and the autophagosome marker LC3. Mutations in this gene are a cause of autosomal recessive congenital cataract 2 (CATC2).