UB2D4 Polyclonal Antibody, 50ul Cell Proliferation and with Joubert syndrome type

and with Joubert syndrome type 4

Mutations that alter the jagged 1 protein cause Alagille syndrome

which is activated by binding of small GTPases such as CDC42 to an N-terminal regulatory domain

which incorporates synthetic genotyping (Synotype) alongside Genotype and Phenotype

Contains 1 kinesin-motor domain

UB2D4 Polyclonal Antibody, 50ul Cell Proliferation and with Joubert syndrome typeCatalytic activity: ATP + ubiquitin + protein lysine = AMP + diphosphate + protein N ubiquityllysine.,Catalyzes the covalent attachment of ubiquitin to other proteins.,pathway: Protein modification; protein ubiquitination.,Belongs to the ubiquitin conjugating enzyme family.,