Mi2- Alpha Monoclonal Antibody, 100ul[BT-MCA0885] Cell Labeling & Imaging 250mLx6pcs

250mLx6pcs

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

This protein localizes to the endoplasmic reticulum and its expression is induced by phenobarbital

apoptosis and transcription regulation

Mi2- Alpha Monoclonal Antibody, 100ul[BT-MCA0885] Cell Labeling & Imaging 250mLx6pcsThis 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.