DHB12 Polyclonal Antibody, 100ul Custom RNA Oligos This gene encodes a member

This gene encodes a member of a subset of aquaporins called the aquaglyceroporins

This gene is deleted in Williams syndrome| a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11

They are abundant in the granules of neutrophils and also found in the epithelia of mucosal surfaces such as those of the intestine

This protein is a member of the Stac gene family and contains an N-terminal cysteine-rich domain and two SH3 domains

Key regulator of adherens junction integrity and differentiation that may be involved in CDH1-mediated adhesion and signaling in epithelial cells

DHB12 Polyclonal Antibody, 100ul Custom RNA Oligos This gene encodes a memberThis gene encodes a very important 17beta hydroxysteroid dehydrogenase (17beta HSD) that converts estrone into estradiol in ovarian tissue. This enzyme is also involved in fatty acid elongation.