S2P Polyclonal Antibody, 100ul Immune Cell Analysis The latter contains multiple phosphorylation

The latter contains multiple phosphorylation sites for protein kinase C

A duplication of this gene is associated with autosomal dominant adult-onset leukodystrophy (ADLD)

Mutations in KAL1 cause the X-linked Kallmann syndrome

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These genes play critical roles during fetal development and cancer growth

S2P Polyclonal Antibody, 100ul Immune Cell Analysis The latter contains multiple phosphorylationMBTPS2 (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