Mi2- Alpha Monoclonal Antibody, 100ul[BT-MCA0885] Cell Labeling & Imaging Mutations in DOK7 are a

Mutations in DOK7 are a cause of familial limb-girdle myasthenia autosomal recessive

which also associates with the herpes simplex virus (HSV) protein VP16 that induces transcription of HSV immediate-early genes

250mLx6pcs

Interacts with PCNT

apoptosis and transcription regulation

Mi2- Alpha Monoclonal Antibody, 100ul[BT-MCA0885] Cell Labeling & Imaging Mutations in DOK7 are aThis gene encodes a member of the CHD family of proteins which are characterized by the presence of chromo (chromatin organization modifier) domains and SNF2 related helicase ATPase domains. This protein is one of the components of a histone deacetylase complex referred to as the Mi 2 NuRD complex which participates in the remodeling of chromatin by deacetylating histones. Chromatin remodeling is essential for many processes including transcription.