S2P Polyclonal Antibody, 50ul Primary Antibodies Cowden syndrome

Cowden syndrome

subcellular location:Present on the membrane of dendrites and cell bodies but excluded from axonal membrane

GTPase Hras undergoes a continuous cycle of de- and re-palmitoylation

The encoded protein may be involved in the regulation of tyrosine kinase receptor signaling

Mutations in this gene cause cardiofaciocutaneous syndrome (CFC syndrome)

S2P Polyclonal Antibody, 50ul Primary Antibodies Cowden syndromeMBTPS2 (membrane bound transcription factor peptidase, site 2) encodes a intramembrane zinc metalloprotease, which is essential in development. This protease functions in the signal protein activation involved in sterol control of transcription and the ER stress response. Mutations in MBTPS2 have been associated with ichthyosis follicularis with atrichia and photophobia (IFAP syndrome); IFAP syndrome has been quantitatively linked to a reduction in