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SNX21 encodes a member of the sorting nexin family. Additionally we are shipping SNX21 Proteins (4) and many more products for this protein.
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Data suggest that human sorting nexin-L (SNX-L) may be a regulatory gene involved in receptor protein degradation during embryonic liver development.
SAXS solution structures of SNX20 (show SNX20 Antibodies) and SNX21 show that the proteins adopt a compact globular architecture; membrane interaction analyses indicate the presence of phosphoinositide -binding sites that may regulate their intracellular localization.
This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region, like some family members. The specific function of this protein has not been determined. Multiple transcript variants encoding distinct isoforms have been identified for this gene.
sorting nexin 21
, sorting nexin L
, sorting nexin-21