Nucleophosmin Polyclonal Antibody, 100ul Liquid Handling ＆Storage Defects in MEF2A could be

Defects in MEF2A could be a cause of autosomal dominant coronary artery disease 1 with myocardial infarction (ADCAD1)

Iδ and Iε

Alternatively spliced transcript variants have been observed but the full-length nature of only one has been determined

CaoV-3 (ovary adenocarcinoma)

which is associated with Borjeson-Forssman-Lehmann syndrome (BFLS)

Nucleophosmin Polyclonal Antibody, 100ul Liquid Handling ＆Storage Defects in MEF2A could beNPM1 encodes a phosphoprotein which moves between the nucleus and the cytoplasm. The gene product is thought to be involved in several processes including regulation of the ARF p53 pathway. A number of genes are fusion partners have been characterized, in particular the anaplastic lymphoma kinase gene on chromosome 2. Mutations in NPM1 are associated with acute myeloid leukemia. More than a dozen pseudogenes of NPM1 have been identified. Alternative