DDX55 Polyclonal Antibody, 100ul Glassware Sets Mutations in CCND2 are associated

Mutations in CCND2 are associated with megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3 (MPPH3)

Sterilized and non-sterilized available sterilized by irradiation to SAL 10^-6

SIX5 is located downstream of the dystrophia myotonica-protein kinase gene

The gene may be regulated by androgens and epigenetic mechanisms

DDX55 Polyclonal Antibody, 100ul Glassware Sets Mutations in CCND2 are associatedDDX55 encodes a member of protein family containing a characteristic Asp Glu Ala Asp (DEAD) motif. These proteins are putative RNA helicases, and may be involved in a range of nuclear processes including translational initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Multiple alternatively spliced transcript variants have been found for DDX55. Pseudogenes have been identified on chromosomes 1 and 12.