GRP1 Polyclonal Antibody, 50ul Molecular Weight Markers Mutations in this gene caused

Mutations in this gene caused an autosomal recessive progressive myoclonic epilepsy-4 (EPM4)

KLF10 (Kruppel like factor 10) encodes a member of a family of proteins that feature C2H2-type zinc finger domains

It also lacks the conserved I-helix motif AGX (D

Adaptins are important components of clathrin-coated vesicles transporting ligand-receptor complexes from the plasma membrane or from the trans-Golgi network to lysosomes

and the development of obesity

GRP1 Polyclonal Antibody, 50ul Molecular Weight Markers Mutations in this gene causedCYTH3 encodes a member of the PSCD (pleckstrin homology, Sec7 and coiled coil domains) family. PSCD family members have identical structural organization that consists of an N terminal coiled coil motif, a central Sec7 domain, and a C terminal pleckstrin homology (PH) domain. The coiled coil motif is involved in homodimerization, the Sec7 domain contains guanine nucleotide exchange protein (GEP) activity, and the PH domain interacts with phospholipids