PRP8 Polyclonal Antibody, 100ul Protein Expression the major source of B

the major source of B cell precursors

This gene is the founding member of the NEDD4 family of HECT ubiquitin ligases that function in the ubiquitin proteasome system of protein degradation

and myelokathexis) syndrome

Mutations in this gene are associated with the autosomal recessive disorders cystic fibrosis and congenital bilateral aplasia of the vas deferens

PRP8 Polyclonal Antibody, 100ul Protein Expression the major source of BPre mRNA splicing occurs in 2 sequential transesterification steps. The protein encoded by this gene is a component of both U2 and U12 dependent spliceosomes, and found to be essential for the catalytic step II in pre mRNA splicing process. It contains several WD repeats, which function in protein protein interactions. This protein has a sequence similarity to yeast Prp8 protein. This gene is a candidate gene for autosomal dominant retinitis