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Phosphatidylinositol Glycan Anchor Biosynthesis, Class N Proteins (PIGN)

PIGN encodes a protein that is involved in glycosylphosphatidylinositol (GPI)-anchor biosynthesis. Additionally we are shipping Phosphatidylinositol Glycan Anchor Biosynthesis, Class N Antibodies (20) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
PIGN 23556 O95427
PIGN 27392  
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Top Phosphatidylinositol Glycan Anchor Biosynthesis, Class N Proteins at antibodies-online.com

Showing 4 out of 4 products:

Catalog No. Origin Source Conjugate Images Quantity Supplier Delivery Price Details
HOST_Escherichia coli (E. coli) Mouse His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 29 to 34 Days
$4,331.68
Details
HOST_Escherichia coli (E. coli) Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 29 to 34 Days
$4,331.68
Details
Insect Cells Mouse rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.25 mg Log in to see 59 to 64 Days
$6,052.17
Details
Insect Cells Human rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.5 mg Log in to see 59 to 64 Days
$8,623.45
Details

PIGN Proteins by Origin and Source

Origin Expressed in Conjugate
Human ,
,
Mouse (Murine) ,
,

More Proteins for Phosphatidylinositol Glycan Anchor Biosynthesis, Class N (PIGN) Interaction Partners

Human Phosphatidylinositol Glycan Anchor Biosynthesis, Class N (PIGN) interaction partners

  1. PIGN mutation is associated with multiple congenital anomalies hypotonia seizures syndrome related epilepsy.

  2. The mutated PIGN caused a significant decrease of the overall glycosylphoshatidylinositol-anchored proteins and CD24 (show CD24 Proteins) expression which is sufficient to cause severe phenotypic expression.

  3. 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.

  4. PIGN encodes phosphatidylinositol-glycan biosynthesis class N protein.

  5. Multiple congenital anomalies-hypotonia-seizures syndrome is caused by a mutation in PIGN.

Phosphatidylinositol Glycan Anchor Biosynthesis, Class N (PIGN) Protein Profile

Protein Summary

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.

Gene names and symbols associated with PIGN

  • morphogenesis checkpoint dependent (MCD4)
  • phosphatidylinositol glycan anchor biosynthesis, class N (PIGN)
  • phosphatidylinositol glycan anchor biosynthesis, class N (Pign)
  • Gm20308 protein
  • MCAHS protein
  • MCAHS1 protein
  • MCD4 protein
  • MDC4 protein
  • PIG-N protein

Protein level used designations for PIGN

hypothetical protein , GPI ethanolamine phosphate transferase 1 , MCD4 homolog , phosphatidylinositol-glycan biosynthesis class N protein , phosphatidylinositol glycan, class N

GENE ID SPECIES
3642036 Candida albicans SC5314
23556 Homo sapiens
27392 Mus musculus
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