MESP2 Polyclonal Antibody, 50ul Lentiviral Packaging disease:Defects in RAD54B may be

disease:Defects in RAD54B may be a cause of tumor formation

Mutations in this gene are associated with several congenital defects

NOTCH2 encodes a member of the Notch family

The encoded protein (BTB domain and CNC homolog 1) contains broad complex

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

MESP2 Polyclonal Antibody, 50ul Lentiviral Packaging disease:Defects in RAD54B may beThis 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