EBP2 Polyclonal Antibody, 20ul Sampling Tubes Defects in this gene are

Defects in this gene are a cause of progressive external ophthalmoplegia with mitochondrial DNA deletions 1 (PEOA1)

The protein encoded by this gene belongs to the Fbxs class and contains an F-box domain

Among its related pathways are Platinum Pathway

ensuring precise and efficient mixing with every use

Members of this Type 1 transmembrane protein family share structural characteristics including an extracellular domain consisting of multiple epidermal growth factor-like (EGF) repeats

EBP2 Polyclonal Antibody, 20ul Sampling Tubes Defects in this gene areRequired for the processing of the 27S pre rRNA.,Belongs to the EBP2 family.,subunit: Specifically interacts with EBV EBNA1. The EBNA1 EBP2 interaction is important for the stable segregation of EBV episomes during cell division.,tissue specificity: Ubiquitous.,