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PIGN encodes a protein that is involved in glycosylphosphatidylinositol (GPI)-anchor biosynthesis. Additionally we are shipping Phosphatidylinositol Glycan Anchor Biosynthesis, Class N Proteins (4) and many more products for this protein.
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Human Polyclonal PIGN Primary Antibody for EIA, WB - ABIN954137
Hong, Maeda, Watanabe, Ohishi, Mishkind, Riezman, Kinoshita: Pig-n, a mammalian homologue of yeast Mcd4p, is involved in transferring phosphoethanolamine to the first mannose of the glycosylphosphatidylinositol. in The Journal of biological chemistry 2000
Show all 4 references for ABIN954137
Findings confirm that developmental delay, hypotonia, and epilepsy combined with congenital anomalies are common phenotypes of PIGN mutations and add progressive cerebellar atrophy to this clinical spectrum.
PIGN encodes phosphatidylinositol-glycan biosynthesis class N protein.
Multiple congenital anomalies-hypotonia-seizures syndrome is caused by a mutation in PIGN.
This gene encodes a protein that is involved in glycosylphosphatidylinositol (GPI)-anchor biosynthesis. The GPI-anchor is a glycolipid found on many blood cells and serves to anchor proteins to the cell surface. This protein is expressed in the endoplasmic reticulum and transfers phosphoethanolamine (EtNP) to the first mannose of the GPI anchor. Two alternatively spliced variants, which encode an identical isoform, have been reported.
, GPI ethanolamine phosphate transferase 1
, MCD4 homolog
, phosphatidylinositol-glycan biosynthesis class N protein
, phosphatidylinositol glycan, class N