Not available outside of the UK & Ireland.
Biochem/physiol Actions
MUSTN1 is involved in bone development and regeneration, as well as chondrogenesis. It is critical in the regulation of myogenic differentiation and myofusion as its knock-down inhibits the processes.
Disclaimer
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
General description
Musculoskeletal, embryonic nuclear protein 1 (MUSTN1) is encoded by the gene is mapped to human chromosome 3p21.1.
MUSTN1 gene was initially discovered in fracture callus tissue. The gene codes for a small nuclear protein and is known to be widely expressed in skeletal muscle. MUSTN1 expression is observed during embryogenesis in the developing muscles and somites. Its maximum expression is observed from the third month of life. The gene is highly conserved among the vertebrates. The gene is known to contain a nuclear localization sequence, phosphorylation and myristoylation sites.
Immunogen
synthetic peptide corresponding to amino acids 6-20of human MUSTN1
Physical form
Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.
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