SOLH1 Rabbit Polyclonal Antibody, 100ul Drying & Desiccation Mutations in STXBP1 have been

Mutations in STXBP1 have been associated with infantile epileptic encephalopathy-4

including neonatal disease and adult-onset neurodegenerative disorders

which are integral membrane glycoproteins that participate in the enterohepatic circulation of bile acids

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phosphorylates sites that trigger the degradation of the inhibitor via the ubiquination pathway

SOLH1 Rabbit Polyclonal Antibody, 100ul Drying & Desiccation Mutations in STXBP1 have beenThis gene encodes one of testis specific transcription factors which are essential for spermatogenesis oogenesis and folliculogenesis. This gene is located on chromosome 9. Mutations in this gene are associated with nonobstructive azoospermia. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.