MBD2 Rabbit Polyclonal Antibody, 50ul Proteases Probable G-protein coupled receptor 171

Probable G-protein coupled receptor 171 is a orphan receptor

belongs to the sevenless subfamily of tyrosine kinase insulin receptor genes

and neonatal-onset multisystem inflammatory disease (NOMID)

Mutations in this gene result in trifunctional protein deficiency or LCHAD deficiency

Dephosphorylates HSPB1 and SSH1

MBD2 Rabbit Polyclonal Antibody, 50ul Proteases Probable G-protein coupled receptor 171DNA methylation is the major modification of eukaryotic genomes and plays an essential role in mammalian development. Human proteins MECP2 MBD1 MBD2 MBD3 and MBD4 comprise a family of nuclear proteins related by the presence in each of a methyl CpG binding domain (MBD). Each of these proteins with the exception of MBD3 is capable of binding specifically to methylated DNA. MECP2 MBD1 and MBD2 can also repress transcription from methylated gene