Determination of MN blood group from blood stains by electrophoresis and immunoblotting

1989 ◽  
Vol 103 (1) ◽  
pp. 21-25
Author(s):  
Fumio Moriya ◽  
Ryo Nanikawa
Keyword(s):  
Blood Group ◽  
Blood Stains ◽  
Mn Blood Group

scholarly journals The role of sialic acid in the expression of human MN blood group antigens.

1979 ◽  
Vol 254 (6) ◽  
pp. 2112-2119 ◽  
Author(s):  
J.E. Sadler ◽  
J.C. Paulson ◽  
R.L. Hill
Keyword(s):  
Sialic Acid ◽  
Blood Group ◽  
Blood Group Antigens ◽  
Mn Blood Group

Primate genes for glycophorins carrying MN blood group antigens

1993 ◽  
Vol 22 (1) ◽  
pp. 7-12
Author(s):  
Shinichi Kudo ◽  
Masaaki Onda ◽  
Ann Rearden ◽  
Minoru Fukuda
Keyword(s):  
Blood Group ◽  
Blood Group Antigens ◽  
Mn Blood Group

Anti-Tm, an Antibody Defining a New Antigenic Determinant within the MN Blood-Group System

Vox Sanguinis ◽  
1965 ◽  
Vol 10 (6) ◽  
pp. 742-743
Author(s):  
P.D. Issitt ◽  
Jane M. Haber ◽  
F.H. Allen jr.
Keyword(s):  
Blood Group ◽  
Antigenic Determinant ◽  
Blood Group System ◽  
Group System ◽  
Mn Blood Group

HLA-restricted lymphoproliferative responses to MN blood group determinants

Nature ◽  
1982 ◽  
Vol 299 (5878) ◽  
pp. 67-69 ◽  
Author(s):  
M. A. Blajchman ◽  
N. Heddle ◽  
N. Naipul ◽  
D. P. Singal
Keyword(s):  
Blood Group ◽  
Mn Blood Group

Enzymatic Determination of the Anomeric Structures of Two Blood-Group B Active Glycosphingolipids Recombined with Apolipoproteins

1978 ◽  
Vol 33 (1-2) ◽  
pp. 73-78 ◽  
Author(s):  
Peter Hanfland ◽  
Gerd Assmann ◽  
Heinz Egge
Keyword(s):  
Blood Group ◽  
Water Solubility ◽  
Erythrocyte Membranes ◽  
High Density Lipoproteins ◽  
Composition Analysis ◽  
Glycosidic Linkage ◽  
Anomeric Configuration ◽  
Enzymatic Determination ◽  
Group B

Abstract Anomeric configuration of oligosaccharides usually is established by specific glycosidases. For this purpose detergents achieving water solubility of primarily insoluble glycosphingolipids as substrates have been replaced by delipidated hum an serum high density lipoproteins. The new method, tested by several well characterized glycosphingolipids and glycosidases, finally was applied to the evaluation of anomeric structures of two blood-group B active glycosphingolipids [ceramide hexa-saccharide (B-I) and ceramide octasaccharide (B -II)] from hum an erythrocyte membranes. In both B-I and B-II, α-glycosidic linkage was dem onstrated for the term inal galactose and fucose residues. β-glycosidic linkage has been evaluated for backbone saccharides. Together with the results pre­ viously obtained by composition analysis, linkage analysis and sequence analysis the following complete structure can be established:B -I: Galα1 → 3Gal (2 ← 1αFuc)β1 → 4GlcNAcβ1 → 3Galβ1 → 4Glcβ1 → 1Cer;B-II: Galα1 → 3Gal (2 ← 1αFuc)β1 → 4GlcNAcβ1 → 3Galβ1 → 4GlcNAcβ1 → 3Galβ1 → 4Glcβ1 → 1Cer.

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