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

CLDN2 (claudin 2) product belongs to the claudin protein family whose members have been identified as major integral membrane proteins localized exclusively at tight junctions

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

Mutations in this gene result in Bietti crystalline corneoretinal dystrophy

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

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)