MNX1 Polyclonal Antibody, 100ul Protein Post-translational Modification and expression of CD9 plays

and expression of CD9 plays a critical role in the suppression of cancer cell motility and metastasis

thyroid hormone receptors and retinoid X receptors

The protein encoded by this gene has sequence homology to members of the histone deacetylase family

This gene is a member of the KCNN family of potassium channel genes

which is characterized by a distinctive mid-hindbrain and cerebellar malformation

MNX1 Polyclonal Antibody, 100ul Protein Post-translational Modification and expression of CD9 playsThis gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.