PDD2L Polyclonal Antibody, 100ul Gloves Two alternatively spliced transcript variants

Two alternatively spliced transcript variants encoding different isoforms have been described for this gene

Defects in this gene are a cause of autosomal dominant centronuclear myopathy (ADCNM)

Spectrins are a family of filamentous cytoskeletal proteins that function as essential scaffold proteins that stabilize the plasma membrane and organize intracellular organelles

they associate with the three catenins

PDD2L Polyclonal Antibody, 100ul Gloves Two alternatively spliced transcript variantsPDCD2L (Programmed Cell Death 2 Like) is a Protein Coding gene. An important paralog of this gene is ENSG00000266953. Over expression suppresses AP1, CREB, NFAT, and NF kB transcriptional activation, and delays cell cycle progression at S phase.