SPB10 Polyclonal Antibody, 50ul Antibody Humanization Mutations in MSX2 are associated

Mutations in MSX2 are associated with parietal foramina 1 and craniosynostosis type 2

Contains 6 LRR (leucine-rich) repeats

neuropeptide Y (NPY)

KPNA2 protein interacts with the NLSs of DNA helicase Q1 and SV40 T antigen and may be involved in the nuclear transport of proteins

SPB10 Polyclonal Antibody, 50ul Antibody Humanization Mutations in MSX2 are associatedThis gene is a member of the serpin peptidase inhibitor, clade B family and is found in a cluster of other similar genes on chromosome 18. The protein encoded by this gene appears to help control the regulation of protease functions during hematopoiesis. Variations in this gene may increase the risk of prostate cancer.