CRGC Rabbit Polyclonal Antibody, 20ul Low retention tips Mutations in RAD50 are the

Mutations in RAD50 are the cause of Nijmegen breakage syndrome-like disorder

Cadherins are a family of adhesion molecules that mediate Ca2+-dependent cell-cell adhesion in all solid tissues and modulate a wide variety of processes

an autosomal recessive disorder characterized by accumulation of delta-1-pyrroline-5-carboxylate (P5C) and proline

HAAO has been suggested to play a role in disorders associated with altered tissue levels of QUIN

transferring phosphorus-containing groups andprotein tyrosine kinase activity

CRGC Rabbit Polyclonal Antibody, 20ul Low retention tips Mutations in RAD50 are theThis gene encodes a member of the beta gamma crystallin family of proteins. Crystallins constitute the major proteins of vertebrate eye lens and maintain the transparency and refractive index of the lens. This gene and several family members are present in a gene cluster on chromosome 2. Mutations in this gene have been shown to cause multiple types of cataract including Coppock like cataract and zonular pulverulent cataract among others.