PPP1R2P3 Polyclonal Antibody, 20ul Antisense Oligonucleotides Mutations in this gene are

Mutations in this gene are associated with Leigh syndrome resulting from mitochondrial complex I deficiency

This protein functions as a lysophosphatidic acid (LPA) receptor and contributes to Ca2+ mobilization

and free from contamination with our DNase/RNase-free packaging

Coagulation factor II (thrombin) receptor-like 3 (F2RL3) is a member of the large family of 7-transmembrane-region receptors that couple to guanosine-nucleotide-binding proteins

Cerebellin family members act as transneuronal regulators of synapse development and synaptic plasticity in various brain regions

PPP1R2P3 Polyclonal Antibody, 20ul Antisense Oligonucleotides Mutations in this gene arePPP1R2P3 (Protein Phosphatase 1 Regulatory Inhibitor Subunit 2 Pseudogene 3) is a Pseudogene. GO annotations related to this gene include protein phosphatase inhibitor activity. nhibitor of protein phosphatase 1.