VSX2 Polyclonal Antibody, 20ul Monoclonal Antibody Preparation Members of the subfamily share

Members of the subfamily share similarity in sequence and splice sites

Deficiencies in this protein are associated with an increased risk of ischemic arterial diseases and fetal loss

at least one of which encodes a preproprotein that is proteolytically processed to generate heavy and light chains that form a disulfide-linked dimer

May recognize and hydrolyze the peptide bond at the C-terminal Gly of ubiquitin

VSX2 Polyclonal Antibody, 20ul Monoclonal Antibody Preparation Members of the subfamily shareThis gene encodes a homeobox protein originally described as a retina specific transcription factor. Mutations in this gene are associated with microphthalmia, cataracts and iris abnormalities.