TSYL2 Polyclonal Antibody, 50ul Microplate Mixer Mutations in STXBP1 have been

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

This transfer activity is required for COPI complex-mediated retrograde transport from the Golgi apparatus to the endoplasmic reticulum

Members of this family function in several sensory systems and regulate blood pressure

as well as bHLH and PAS domains

TSYL2 Polyclonal Antibody, 50ul Microplate Mixer Mutations in STXBP1 have beenThis gene encodes a member of the testis specific protein Y encoded, TSPY like SET nucleosome assembly protein 1 superfamily. The encoded protein is localized to the nucleolus where it functions in chromatin remodeling and as an inhibitor of cell cycle progression. This protein may play a role in the suppression of tumor growth.