MISSL Rabbit Polyclonal Antibody, 100ul Pipette Filler Mutations in CEP135 are associated

Mutations in CEP135 are associated with autosomal recessive primary microcephaly-8

is a 2271 amino acid protein that is homologous to the S

The folate receptor 1 encoded by FOLR1 is a member of the folate receptor family

These enzymes are part of a multicomponent integral membrane system that catalyzes the hydrolysis of glucose-6-phosphate| the terminal step in gluconeogenic and glycogenolytic pathways| allowing the release of glucose into the bloodstream

ERBB4 is a member of the Tyr protein kinase family and the epidermal growth factor receptor subfamily

MISSL Rabbit Polyclonal Antibody, 100ul Pipette Filler Mutations in CEP135 are associated