FPR2 Polyclonal Antibody, 100ul Monoclonal Antibodies Mutations in this gene have

Mutations in this gene have been associated with neonatal diabetes and congenital hypothyroidism (NDH)

|subunit:The two chains are formed from a single-chain precursor by the excision of two Arg residues and are held together by 1 or more disulfide bonds

The members of this family are not expressed in normal tissues

This association links the cadherin protein to the cytoskeleton

The encoded protein may play a role in regulating p53-mediated apoptosis

FPR2 Polyclonal Antibody, 100ul Monoclonal Antibodies Mutations in this gene haveLow affinity receptor for N formyl methionyl peptides, which are powerful neutrophils chemotactic factors. Binding of FMLP to the receptor causes activation of neutrophils. This response is mediated via a G protein that activates a phosphatidylinositol calcium second messenger system. The activation of LXA4R could result in an anti inflammatory outcome counteracting the actions of proinflammatory signals such as LTB4 (leukotriene B4).,Belongs to the G