S2P Polyclonal Antibody, 100ul Immune Cell Analysis The CD1 family members are

The CD1 family members are thought to differ in their cellular localization and specificity for particular lipid ligands

Mutations in these genes have been associated with White Sponge Nevus

This gene is expressed exclusively in the brain

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Mutations in KAL1 cause the X-linked Kallmann syndrome

S2P Polyclonal Antibody, 100ul Immune Cell Analysis The CD1 family members areMBTPS2 (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