p73(Phospho Tyr99) Polyclonal Antibody, 20ul Dry Bath Compact and portable

Compact and portable

Mutations in this gene are the cause of spondylometaphyseal and metatropic dysplasia and hereditary motor and sensory neuropathy type IIC

The functions of human sirtuins have not yet been determined

heterodimeric serine protease comprised of heavy and light chains

SCML2 encodes a member of the Polycomb group proteins

p73(Phospho Tyr99) Polyclonal Antibody, 20ul Dry Bath Compact and portableThis gene encodes a member of the p53 family of transcription factors involved in cellular responses to stress and development. It maps to a region on chromosome 1p36 that is frequently deleted in neuroblastoma and other tumors, and thought to contain multiple tumor suppressor genes. The demonstration that this gene is monoallelically expressed (likely from the maternal allele), supports the notion that it is a candidate gene for neuroblastoma. Many