SH3G3 Polyclonal Antibody, 100ul Cellular Function Assays Velocardiofacial syndrome (VCFS) is a

Velocardiofacial syndrome (VCFS) is a developmental disorder characterized by conotruncal heart defects

a disease characterized by recurrent bacterial infections

Embark on a daring journey with Trypsin-EDTA Solution with phenol red

This gene is a member of the prenyltransferase family and encodes a protein with geranylgeranyl diphosphate (GGPP) synthase activity

Defects in this gene are a cause of epilepsy female-restricted with mental retardation (EFMR)

SH3G3 Polyclonal Antibody, 100ul Cellular Function Assays Velocardiofacial syndrome (VCFS) is aAn N terminal amphipathic helix, the BAR domain and a second amphipathic helix inserted into helix 1 of the BAR domain (N BAR domain) induce membrane curvature and bind curved membranes.,Implicated in endocytosis. May recruit other proteins to membranes with high curvature.,Belongs to the endophilin family.,Contains 1 BAR domain.,Contains 1 SH3 domain.,subcellular location: Associated with postsynaptic endosomes in hippocampal neurons. Associated with