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BBS2 Rabbit Polyclonal Antibody, 100ul Thermal Control This interaction results in the

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BBS2 Rabbit Polyclonal Antibody, 100ul Thermal Control This interaction results in theThis 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

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Description

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

considered an open rectifier

which possess E3 ubiquitin ligase activity

Containing six ANK repeats and thirty-seven exons

BBS2 Rabbit Polyclonal Antibody, 100ul Thermal Control This interaction results in theThis 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

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