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

A must-have for any lab or research facility

Four alternatively spliced transcript variants encoding distinct isoforms have been reported

This complex facilitates the recruitment of mRNA to the ribosome

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

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)