GlyRBeta Polyclonal Antibody, 20ul Lysosome The last exon of this

The last exon of this gene overlaps with the CD3e molecule

An important paralog of this gene is GK

our PES Express Membrane ensures fast and reliable filtration

The physiological role of chloride channel 4 remains unknown but may contribute to the pathogenesis of neuronal disorders

The protein is an integral membrane protein and is one of the entry cofactors for hepatitis C virus

GlyRBeta Polyclonal Antibody, 20ul Lysosome The last exon of thisGLRB encodes the beta subunit of the glycine receptor, which is a pentamer composed of alpha and beta subunits. The receptor functions as a neurotransmitter gated ion channel, which produces hyperpolarization via increased chloride conductance due to the binding of glycine to the receptor. Mutations in this gene cause startle disease, also known as hereditary hyperekplexia or congenital stiff person syndrome, a disease characterized by muscular