NPTX2 Polyclonal Antibody, 20ul Palm Micro Centrifuges Mutations in this gene cause

Mutations in this gene cause early infantile epileptic encephalopathy 25

This gene encodes a capillary endothelial cell protein that facilitates the lipolytic processing of triglyceride-rich lipoproteins

Mammalian mitochondrial ribosomal protein L 12 (39S ribosomal protein L12 mitochondrial) is encoded by nuclear gene MRPL12 and help in protein synthesis within the mitochondrion

Its primary role is in fatty acid elongation or complex lipid synthesis rather than in degradation

hearing loss

NPTX2 Polyclonal Antibody, 20ul Palm Micro Centrifuges Mutations in this gene causeThis gene encodes a member of the family of neuronal petraxins, synaptic proteins that are related to C reactive protein. This protein is involved in excitatory synapse formation. It also plays a role in clustering of alpha amino 3 hydroxy 5 methyl 4 isoxazolepropionic acid (AMPA) type glutamate receptors at established synapses, resulting in non apoptotic cell death of dopaminergic nerve cells. Up regulation of this gene in Parkinson disease (PD)