APOC4 Polyclonal Antibody, 100ul sgRNA customized design Mutations in this gene are

Mutations in this gene are associated with Bardet-Biedl syndrome (BBS)

are enclosed in double-membrane structures called autophagosomes and delivered to lysosomes or vacuoles for degradation

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CYSLTR1 encodes a member of the G-protein coupled receptor 1 family

This protein plays an essential role in regulating developmental pathways during embryogenesis

APOC4 Polyclonal Antibody, 100ul sgRNA customized design Mutations in this gene areThis gene encodes a lipid binding protein belonging to the apolipoprotein gene family. The protein is thought to play a role in lipid metabolism. Polymorphisms in this gene may influence circulating lipid levels and may be associated with coronary artery disease risk. This gene is present in a cluster with other related apolipoprotein genes on chromosome 19. Naturally occurring read through transcription exists between this gene and the neighboring