MESP2 Polyclonal Antibody, 50ul Lentiviral Packaging Mutations in this gene are

Mutations in this gene are associated with several congenital defects

KDR/Flk-1 and Flt-4 are members of the class III subfamily of RTKs containing seven immunoglobulin-like repeats in their extracellular domains

infections and cancer

This gene belongs to the forkhead family of transcription factors which are characterized by a distinct forkhead domain

and alloimmune neonatal neutropenia

MESP2 Polyclonal Antibody, 50ul Lentiviral Packaging Mutations in this gene areThis gene encodes a member of the bHLH family of transcription factors and plays a key role in defining the rostrocaudal patterning of somites via interactions with multiple Notch signaling pathways. This gene is expressed in the anterior presomitic mesoderm and is downregulated immediately after the formation of segmented somites. This gene also plays a role in the formation of epithelial somitic mesoderm and cardiac mesoderm. Mutations in the MESP2