Smad3 Polyclonal Antibody, 100ul[BT-AP08392] Pathway and Network Analysis SIGLEC5 encodes a member of

SIGLEC5 encodes a member of the sialic acid-binding immunoglobulin-like lectin (Siglec) family

Mutations in this gene have been associated with KBG syndrome| which is characterized by macrodontia| distinctive craniofacial features| short stature| skeletal anomalies| global developmental delay| seizures and intellectual disability

Isoform 1 has lower affinity for DNA

Gel-forming glycoprotein of gastric and respiratoy tract epithelia that protects the mucosa from infection and chemical damage by binding to inhaled microrganisms and particules that are subsequently removed by the mucocilary system

This gene encodes a member of the lysophospholipid acyltransferase family

Smad3 Polyclonal Antibody, 100ul[BT-AP08392] Pathway and Network Analysis SIGLEC5 encodes a member ofThe protein encoded by SMAD3 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 functions as a transcriptional modulator activated by transforming growth factor beta and is thought to play a role in the regulation of