CLD23 Polyclonal Antibody, 20ul Polyclonal Antibody Preparation Defects in PEX19 are a

Defects in PEX19 are a cause of Zellweger syndrome (ZWS)

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A pseudogene of MED21 is located on chromosome 8

CLD23 Polyclonal Antibody, 20ul Polyclonal Antibody Preparation Defects in PEX19 are aThis gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. This gene is expressed in germinal center B cells, placenta