CRGC Rabbit Polyclonal Antibody, 20ul Low retention tips an autosomal recessive disorder characterized

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

TNXB localizes to the major histocompatibility complex (MHC) class III region on chromosome 6

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

Pphosphatase and tensin homolog encoded by PTEN is a phosphatidylinositol-3

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

CRGC Rabbit Polyclonal Antibody, 20ul Low retention tips an autosomal recessive disorder characterizedThis 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.