PRP8 Polyclonal Antibody, 100ul Protein Expression Mutations in this gene are

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

and was revealed to be the trabecular meshwork glucocorticoid-inducible response protein (TIGR)

This gene likely encodes a member of the complexin family

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

The heat shock protein family B (small) member 1 encoded by HSPB1 is induced by environmental stress and developmental changes

PRP8 Polyclonal Antibody, 100ul Protein Expression Mutations in this gene arePre 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