PAR-3 Polyclonal Antibody, 100ul RNA Tools craniofacial anomalies

craniofacial anomalies

TAS2R43 belongs to the large TAS2R receptor family

and functions to induce apoptosis

Mutations in this gene cause autosomal dominant severe congenital neutropenia

severe spinal curvature

PAR-3 Polyclonal Antibody, 100ul RNA Tools craniofacial anomaliesF2RL2 encodes a member of the protease activated receptor (PAR) family which is a subfamily of the seven transmembrane G protein coupled cell surface receptor family. The coagulation factor II thrombin receptor like 2 acts as a cofactor in the thrombin mediated cleavage and activation of the protease activated receptor family member PAR4. The encoded protein plays an essential role in hemostasis and thrombosis. Alternate splicing results in multiple