Neuropilin-2 Polyclonal Antibody, 50ul[BT-AP05938] Molecular Biology Mucopolysaccharidosis type VI is an

Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B

CNP-29 and CNP-22

This gene encodes a member of the globin superfamily and is expressed in skeletal and cardiac muscles

which activates NF-kappa-B by making it available to translocate to the nucleus

Studies of the mouse counterpart of this gene suggested that this kinase play a key role in T cell proliferation

Neuropilin-2 Polyclonal Antibody, 50ul[BT-AP05938] Molecular Biology Mucopolysaccharidosis type VI is anNRP2 encodes a member of the neuropilin family of receptor proteins. The encoded transmembrane protein binds to SEMA3C protein {sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C} and SEMA3F protein {sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F}, and interacts with vascular endothelial growth factor (VEGF). This protein may play a role in cardiovascular development, axon