RARBeta Polyclonal Antibody, 20ul ADME Defects in PPT1 are a

Defects in PPT1 are a cause of infantile neuronal ceroid lipofuscinosis 1 (CLN1

Diacylglycerol kinase theta encoded by DGKQ contains three cysteine-rich domains

but not mononuclear cells or neutrophils

and a pseudogene of MED27 is located on the long arm of chromosome 5

which is an ubiquitin-conjugating enzyme required for post-replication repair of damaged DNA

RARBeta Polyclonal Antibody, 20ul ADME Defects in PPT1 are aRARB encodes retinoic acid receptor beta, a member of the thyroid steroid hormone receptor superfamily of nuclear transcriptional regulators. This receptor localizes to the cytoplasm and to subnuclear compartments. It binds retinoic acid, the biologically active form of vitamin A which mediates cellular signalling in embryonic morphogenesis, cell growth and differentiation. It is thought that this protein limits growth of many cell types by regulating