PAR-3 Polyclonal Antibody, 50ul Multiplex Immunoassays Mutations in MTR have been

Mutations in MTR have been identified as the underlying cause of methylcobalamin deficiency complementation group G

Recruitment of this protein to the plasma membrane occurs in a lysophosphatidic acid (LPA)-dependent manner and it regulates LPA-induced cell migration

May be involved in pre-mRNA splicing

it does bind tightly to other ligand-bound EGF receptor family members to form a heterodimer

The encoded protein binds to the enhancer region of the insulin gene

PAR-3 Polyclonal Antibody, 50ul Multiplex Immunoassays Mutations in MTR have beenF2RL2 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