Collagen I mouse Monoclonal Antibody(4H10), 100ul Cell Culture Plates Mutations in this gene cause

Mutations in this gene cause rhabdoid tumor predisposition syndrome type 2

Knockout studies of the similar gene in mice implied the role of this protein in regulating proliferation and differentiation of midline cerebellar structures

The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol| steroids and other lipids

Mutations in CLDN5 have been found in patients with velocardiofacial syndrome

Three subunits (alpha| beta and gamma) of the 11S regulator have been identified

Collagen I mouse Monoclonal Antibody(4H10), 100ul Cell Culture Plates Mutations in this gene causeThis gene encodes the pro alpha1 chains of type I collagen whose triple helix comprises two alpha1 chains and one alpha2 chain. Type I is a fibril forming collagen found in most connective tissues and is abundant in bone, cornea, dermis and tendon. Mutations in this gene are associated with osteogenesis imperfecta types I IV, Ehlers Danlos syndrome type VIIA, Ehlers Danlos syndrome Classical type, Caffey Disease and idiopathic osteoporosis. Reciprocal