Smad1 Polyclonal Antibody, 20ul[BT-AP08374] Diagnostic Probes & Oligos Defects in this gene are

Defects in this gene are a cause of pulmonary alveolar microlithiasis

NME1 (NME1) was identified because of its reduced mRNA transcript levels in highly metastatic cells

Ephrin receptors and their ligands

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

This gene is expressed from at least five alternative promoters that are expressed in a tissue-dependent manner

Smad1 Polyclonal Antibody, 20ul[BT-AP08374] Diagnostic Probes & Oligos Defects in this gene areSMAD family member 1 encoded by SMAD1 belongs to the SMAD, a family of proteins similar to the gene products of the Drosophila gene mothers against decapentaplegic' (Mad) and the C. elegans gene Sma. SMAD proteins are signal transducers and transcriptional modulators that mediate multiple signaling pathways. This protein mediates the signals of the bone morphogenetic proteins (BMPs), which are involved in a range of biological activities including