ALDH3B1 Polyclonal Antibody, 100ul Measuring Instruments Mutations in this gene are

Mutations in this gene are the cause of spondylometaphyseal and metatropic dysplasia and hereditary motor and sensory neuropathy type IIC

This PTP was thought to play roles in cell-cell recognition and adhesion

It therefore controls the peroxisomal beta-oxidation pathway of fatty acids

CLCNKA is a member of the CLC family of voltage-gated chloride channels

8-oxoGua is an oxidized form of guanine that can potentially alter genetic information by pairing with adenine and cytosine in RNA

ALDH3B1 Polyclonal Antibody, 100ul Measuring Instruments Mutations in this gene areALDH3B1 encodes a member of the aldehyde dehydrogenase protein family. Aldehyde dehydrogenases are a family of isozymes that may play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. The encoded protein (aldehyde dehydrogenase 3 family member B1) is able to oxidize long chain fatty aldehydes in vitro, and may play a role in protection from oxidative stress. Alternative splicing results in multiple