PINK1 Polyclonal Antibody, 100ul Custom Peptide Synthesis and a C-terminal STAR-related lipid

and a C-terminal STAR-related lipid transfer (START) domain

Mutations in this gene are associated with neurofibromatosis type II which is characterized by nervous system and skin tumors and ocular abnormalities

Binds to the N-terminus of telomeric TERF1 via the ANK repeats

and the development of obesity

NPHS1 encodes a member of the immunoglobulin family of cell adhesion molecules that functions in the glomerular filtration barrier in the kidney

PINK1 Polyclonal Antibody, 100ul Custom Peptide Synthesis and a C-terminal STAR-related lipidThis gene encodes a serine threonine protein kinase that localizes to mitochondria. It is thought to protect cells from stress induced mitochondrial dysfunction. Mutations in this gene cause one form of autosomal recessive early onset Parkinson disease.