MESP2 Polyclonal Antibody, 20ul ADME p21 activated kinase

p21 activated kinase

TNFSF9/4-1BBL

HSF4 lacks the carboxyl-terminal hydrophobic repeat which is shared among all vertebrate HSFs and has been suggested to be involved in the negative regulation of DNA binding activity

Mutations in this gene lead to Meesmann corneal dystrophy

is located at the growth hormone locus on chromosome 17 where they are interspersed in the same transcriptional orientation

MESP2 Polyclonal Antibody, 20ul ADME p21 activated kinaseThis 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