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The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
This 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 gene cause autosomal recessive spondylocostal dystosis 2 (SCD02).
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: bHLHc6; Class C basic helix-loop-helix protein 6; mesoderm posterior 2 homolog; mesoderm posterior basic helix-loop-helix transcription factor 2; Mesoderm posterior protein 2
基因别名: BHLHC6; MESP2; SCDO2
UniProt ID: (Human) Q0VG99, (Mouse) O08574
Entrez Gene ID: (Human) 145873, (Rat) 293046, (Mouse) 17293