GPR32 Polyclonal Antibody, 20ul Recombinant Protein Mutations in SPTAN1 are the

Mutations in SPTAN1 are the cause of early infantile epileptic encephalopathy-5

Members in this family are characterized by their structure (evolutionarily highly conserved TIM barrel) and function (NAD (P)H-dependent oxido-reduction of carbonyl groups)

The encoded preproprotein is proteolytically processed to generate light and heavy chains that comprise the alpha V subunit

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GPR32 Polyclonal Antibody, 20ul Recombinant Protein Mutations in SPTAN1 are theGPR32 is intronless and encodes a member of the G protein coupled receptor 1 family. The G protein coupled receptor 32 binds to resolvin D1 and lipoxin A4 and has been linked to pulmonary inflammation. A related pseudogene has been identified on chromosome 19.