Rad18 Polyclonal Antibody, 20ul Cell Culture & Maintenance Mutations in KCNT1 cause the

Mutations in KCNT1 cause the early-onset epileptic disorders

CARD6 encodes a protein that contains a caspase recruitment domain (CARD)

such as Waardenburg syndrome type 2 and Tietz syndrome

spindle orientation

It is a member of the group-II aristaless-related protein family whose members are expressed primarily in the central and/or peripheral nervous system

Rad18 Polyclonal Antibody, 20ul Cell Culture & Maintenance Mutations in KCNT1 cause theRAD18, E3 ubiquitin protein ligase encoded by RAD18 is highly similar to S. cerevisiae DNA damage repair protein Rad18. Yeast Rad18 functions through its interaction with Rad6, which is an ubiquitin conjugating enzyme required for post replication repair of damaged DNA. Similar to its yeast counterpart, RAD18, E3 ubiquitin protein ligase is able to interact with the human homolog of yeast Rad6 protein through a conserved ring finger motif. Mutation of