MeCP2 Polyclonal Antibody, 100ul Cellular Function Assays Mutations in this gene result

Mutations in this gene result in autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions

Barrett's esophagus as well as in gastric metaplasia of the duodenum (GMD)

epidermal growth factor receptor

The UBP domain of USP13 contains a catalytic site

NFIA encodes a member of the NF1 (nuclear factor 1) family of transcription factors

MeCP2 Polyclonal Antibody, 100ul Cellular Function Assays Mutations in this gene resultDNA methylation is the major modification of eukaryotic genomes and plays an essential role in mammalian development. Human proteins MECP2, MBD1, MBD2, MBD3, and MBD4 comprise a family of nuclear proteins related by the presence in each of a methyl CpG binding domain (MBD). Each of these proteins, with the exception of MBD3, is capable of binding specifically to methylated DNA. MECP2, MBD1 and MBD2 can also repress transcription from methylated gene