Function
Involved in the negative regulation of dendrite outgrowth.
Biological Context
Subcellular Location: Cytoplasm
Disease Association: Ritscher-Schinzel syndrome 4 (RTSC4) : An autosomal dominant form of Ritscher-Schinzel syndrome, a developmental malformation syndrome characterized by cerebellar brain anomalies associated with global developmental delay and impaired intellectual development, congenital heart defects, and craniofacial abnormalities. [The disease is caused by variants affecting the gene represented in this entry]
Product Specifications
Recombinant Human Dihydropyrimidinase-related protein 5 (DPYSL5) is a recombinant protein from Homo sapiens (Human), expressed in E.coli, covering amino acids 1-564aa, with N-terminal 10xHis-tagged and C-terminal Myc-tagged tag, molecular weight 66.4kDa, purity Greater than 85% as determined by SDS-PAGE.. Suitable for ELISA and Western Blot applications.
