RPR1B Rabbit Polyclonal Antibody, 50ul Protein Post-translational Modification Cooperates with PPP2CA to protect

Cooperates with PPP2CA to protect centromeric cohesin from separase-mediated cleavage in oocytes specifically during meiosis I

This gene is located on a region of chromosome 17q21

Mutations in this gene cause selective T-cell defect| a severe combined immunodeficiency disease characterized by a selective absence of CD8-positive T-cells

Expansion of a polyalanine tract and other mutations in this gene cause X-linked mental retardation and epilepsy

indicating the implication of this gene in postmenopausal osteoporosis

RPR1B Rabbit Polyclonal Antibody, 50ul Protein Post-translational Modification Cooperates with PPP2CA to protect