S2P Polyclonal Antibody, 100ul Immune Cell Analysis This gene encodes a protein

This gene encodes a protein with significant sequence similarity to the ligand binding domain of platelet-derived growth factor receptor beta

Mutations in KAL1 cause the X-linked Kallmann syndrome

Mutations in these genes have been associated with White Sponge Nevus

Diseases associated with C2orf40 include esophageal cancer

These genes play critical roles during fetal development and cancer growth

S2P Polyclonal Antibody, 100ul Immune Cell Analysis This gene encodes a proteinMBTPS2 (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