LOXL3 Rabbit Polyclonal Antibody, 20ul sgRNA Library Construction among calpactin I light chain

among calpactin I light chain

Mutations in this gene are associated with pyruvate dehydrogenase E1-alpha deficiency and X-linked Leigh syndrome

Mutations in ABHD12 are associated with the neurodegenerative disease

Some transcripts that skip the last exon of the upstream gene (TNFSF12) and continue into the second exon of TNFSF13 have been identified

LOXL3 Rabbit Polyclonal Antibody, 20ul sgRNA Library Construction among calpactin I light chainThis gene encodes a lysyl oxidase which likely functions as an amine oxidase and plays a role in the formation of crosslinks in collagens and elastin. Deletion of the related gene in mouse causes neonatal mortality with cleft palate spine deformity and defects in collagen organization. A mutation in this gene was found in a family with Stickler syndrome.