MMP13 (Cleaved-Tyr104) Rabbit Polyclonal Antibody, 50ul Gene Editing Defects in POU4F3 are the

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

There is a pseudogene for ALMS1 located adjacent in the same region of chromosome 2

and directly interacts with the tumor suppressor p53 to reduce p53 transcriptional activity by reducing p53 protein level in the absence of DNA damage

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

MMP13 (Cleaved-Tyr104) Rabbit Polyclonal Antibody, 50ul Gene Editing Defects in POU4F3 are 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)