S2P Polyclonal Antibody, 50ul Primary Antibodies subcellular location:Present on the membrane

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

Mutations in this gene cause cardiofaciocutaneous syndrome (CFC syndrome)

but plays an important role in regulating the mechanical stability of red cells

alternative products:The splicing pattern is cell-lineage dependent

S2P Polyclonal Antibody, 50ul Primary Antibodies subcellular location:Present on the membraneMBTPS2 (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