BMPER Polyclonal Antibody, 20ul Molecular Sciences fetal heart and fetal spleen

fetal heart and fetal spleen

Mutations in this gene are known to cause Parkinson disease and autosomal recessive juvenile Parkinson disease

Decreased expression of this gene is associated with splenic marginal zone lymphomas

LIFR encodes leukemia inhibitory factor receptor alpha that belongs to the type I cytokine receptor family

Mutations in this gene are associated with cerebral palsy spastic quadriplegic type 5 (CPSQ5) disorder

BMPER Polyclonal Antibody, 20ul Molecular Sciences fetal heart and fetal spleenThis gene encodes a secreted protein that interacts with, and inhibits bone morphogenetic protein (BMP) function. It has been shown to inhibit BMP2 and BMP4 dependent osteoblast differentiation and BMP dependent differentiation of the chondrogenic cells. Mutations in this gene are associated with a lethal skeletal disorder, diaphanospondylodysostosis.