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Glycophorin C (GYPC) is an integral membrane glycoprotein. Additionally we are shipping Glycophorin C (Gerbich Blood Group) Antibodies (141) and many more products for this protein.
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Plasmodium falciparum STEVOR functions as an erythrocyte-binding protein that recognizes Glycophorin C (GPC) on the red blood cell (RBC (show CACNA1C Proteins)) surface and that its binding correlates with the level of GPC on the RBC (show CACNA1C Proteins) surface.
Rosetting assays using CD236R knockdown normocytes derived from hematopoietic stem cells further supports the role of glycophorin C as a receptor in P vivax rosette formation.
Precise definition of the binding site for the EBA-140 ligand on glycophorin C may be important with respect to human erythrocyte invasion inhibition strategies based on a receptor.
Glycophorin C delta (exon3) is not associated with protection against severe anaemia in Papua New Guinea.
The Gerbich blood group (show DARC Proteins) system
The molecular evolution of GYPC among the Hominoidea (Greater and Lesser Apes) and the pattern of polymorphism at the locus in a global human sample, were examined.
Recombinant Ge2, Ge3 & Ge4 antigens were cloned, expressed and purified. Yus and Ge mutants behaved in SDS (show SDS Proteins)-PAGE similarly to normal GPC forms with diffuse glycosylation.
Data show that the receptor for Plasmodium falciparum erythrocyte-binding antigen 140 (EBA140) is glycophorin C (GYPC) and that this interaction mediates a principal P. falciparum invasion pathway into human erythrocytes.
Glycophorin C is identified as the receptor for PfEBP-2, the erythrocyte binding ligand of Plasmodium falciparum, and the binding domain on GPC is determined to be amino acid residues 14 through 22 within exon 2.
A high GYPC gene expression is associated with an unfavorable outcome, in contrast, a high TRIP3 (show ZNHIT3 Proteins) gene expression is associated with a favorable outcome in childhood ALL.
Glycophorin C (GYPC) is an integral membrane glycoprotein. It is a minor species carried by human erythrocytes, but plays an important role in regulating the mechanical stability of red cells. A number of glycophorin C mutations have been described. The Gerbich and Yus phenotypes are due to deletion of exon 3 and 2, respectively. The Webb and Duch antigens, also known as glycophorin D, result from single point mutations of the glycophorin C gene. The glycophorin C protein has very little homology with glycophorins A and B. Alternate splicing results in multiple transcript variants.
, Gerbich antigen
, glycoprotein beta
, sialoglycoprotein D