P504S Rabbit Polyclonal Antibody, 100ul Microbial Genome Editing Mutations in CA8 are associated

Mutations in CA8 are associated with cerebellar ataxia

SLC9A9 encodes a sodium/proton exchanger that is a member of the solute carrier 9 protein family

phosphodiesterase 4C plays a key role in many important physiological processes

Cytochrome P450 family 4 subfamily A member 11 localizes to the endoplasmic reticulum and hydroxylates medium-chain fatty acids such as laurate and myristate

P504S Rabbit Polyclonal Antibody, 100ul Microbial Genome Editing Mutations in CA8 are associatedThis gene encodes a racemase. The encoded enzyme interconverts pristanoyl CoA and C27 bile acylCoAs between their (R) and (S) stereoisomers. The conversion to the (S) stereoisomers is necessary for degradation of these substrates by peroxisomal beta oxidation. Encoded proteins from this locus localize to both mitochondria and peroxisomes. Mutations in this gene may be associated with adult onset sensorimotor neuropathy pigmentary retinopathy and