MMP13 (Cleaved-Tyr104) Rabbit Polyclonal Antibody, 50ul Gene Editing Complex I functions in the

Complex I functions in the transfer of electrons from NADH to the respiratory chain

and in left-right axis determination

where it catalyzes the esterification of all-trans-retinol into all-trans-retinyl ester

Defects in POU4F3 are the cause of non-syndromic sensorineural deafness autosomal dominant type 15

This complex facilitates the recruitment of mRNA to the ribosome

MMP13 (Cleaved-Tyr104) Rabbit Polyclonal Antibody, 50ul Gene Editing Complex I functions in thecofactor: Binds 2 zinc ions per subunit. cofactor: Binds 4 calcium ions per subunit. disease: Defects in MMP13 are the cause of spondyloepimetaphyseal dysplasia type 2 (SEMD2)