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

an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid

partially responsive to ATP

One of the classes is represented by the proteins ACT2 and ACT8

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.