PRP8 Polyclonal Antibody, 100ul Protein Expression Alternative splicing of transcripts from

Alternative splicing of transcripts from this gene results in multiple transcript variants

and cortical function

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

3-benzoylpyridine

Deficiencies in this protein are associated with an increased risk of ischemic arterial diseases and fetal loss

PRP8 Polyclonal Antibody, 100ul Protein Expression Alternative splicing of transcripts fromPre 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