Mesp2 抗体
(Mesoderm Posterior 2 Homolog (Mesp2))
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). [provided by RefSeq, Oct 2008].
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11 results :
Mesp2
适用: 人
ELISA
宿主: 小鼠
Monoclonal
1B3F9
unconjugated
2 references
Latest Publications for our Mesp2 抗体
: "Mutation analysis of MESP2, HES7 and DUSP6 gene exons in patients with congenital scoliosis." in: Studies in health technology and informatics, Vol. 176, pp. 52-5, (2012) (PubMed).: "Mutations in the MESP2 gene cause spondylothoracic dysostosis/Jarcho-Levin syndrome." in: American journal of human genetics, Vol. 82, Issue 6, pp. 1334-41, (2008) (PubMed).
: "Cardiac commitment of primate embryonic stem cells." in: Nature protocols, Vol. 3, Issue 9, pp. 1381-7, (2008) (PubMed).
Aliases for Mesp2 抗体
mesoderm posterior 2 (Mesp2) 抗体mesoderm posterior bHLH transcription factor 2 (Mesp2) 抗体
mesoderm posterior bHLH transcription factor 2 (MESP2) 抗体
bHLHc6 抗体
SCDO2 抗体
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