BBS2 Rabbit Polyclonal Antibody, 100ul Thermal Control and deletions at this locus

and deletions at this locus are also associated with a decrease in aminoacylase activity

Say goodbye to outdated methods and hello to efficient and reliable digestion

This interaction results in the expression of the catalytic subunit of gamma-glutamylcysteine synthetase

Containing six ANK repeats and thirty-seven exons

BBS2 Rabbit Polyclonal Antibody, 100ul Thermal Control and deletions at this locusThis gene is a member of the Bardet Biedl syndrome (BBS) gene family. Bardet Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and mental retardation. The proteins encoded by BBS gene family members are structurally diverse and the similar phenotypes exhibited by mutations in BBS gene family members is likely due to their shared roles in cilia formation and