PITX3 Polyclonal Antibody, 100ul Peripheral Blood Separation Tube Order now and embark on

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Mutations in this gene have been associated with Kenny-Caffey syndrome (KCS) type 2 and the more severe osteocraniostenosis (OCS| also known as Gracile Bone Dysplasia)| both characterized by short stature| hypoparathyroidism| bone development abnormalities| and hypocalcemia

It encodes a protein (adiponectin

Isoforms Ialpha and Ibeta have identical cGMP-bindin

PITX3 Polyclonal Antibody, 100ul Peripheral Blood Separation Tube Order now and embark onThis gene encodes a member of the RIEG PITX homeobox family, which is in the bicoid class of homeodomain proteins. Members of this family act as transcription factors. This protein is involved in lens formation during eye development. Mutations of this gene have been associated with anterior segment mesenchymal dysgenesis and congenital cataracts.