PHLD Polyclonal Antibody, 20ul Nucleic Acid Amplification Defects in TMEM237 are a

Defects in TMEM237 are a cause of Joubert syndrome-14

Cells adhere strongly to the surface because of the advanced hydrophilic treatment

HOXB9 is a member of the Abd-B homeobox family and encodes a protein with a homeobox DNA-binding domain

This gene encodes a member of the ARID (AT-rich interaction domain) family of DNA binding proteins

It may function as a blood platelet activation marker

PHLD Polyclonal Antibody, 20ul Nucleic Acid Amplification Defects in TMEM237 are aMany proteins are tethered to the extracellular face of eukaryotic plasma membranes by a glycosylphosphatidylinositol (GPI) anchor. The GPI anchor is a glycolipid found on many blood cells. The protein encoded by this gene is a GPI degrading enzyme. Glycosylphosphatidylinositol specific phospholipase D1 hydrolyzes the inositol phosphate linkage in proteins anchored by phosphatidylinositol glycans, thereby releasing the attached protein from the plasma