1970
DOI: 10.2183/pjab1945.46.803
|View full text |Cite
|
Sign up to set email alerts
|

Immunological Properties of “Bombay” Phenotype

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

1975
1975
2002
2002

Publication Types

Select...
4
1

Relationship

0
5

Authors

Journals

citations
Cited by 7 publications
(2 citation statements)
references
References 5 publications
0
2
0
Order By: Relevance
“…These inhibiting patterns seem to be similar to those observed with eel serum and Lotus lectin (Watkins & Morgan, 1962), both of which are specific for fucose linked 1-*-2 to galactose (i.e., H-determinant structure). The following sugars failed to give significant inhibition when tested up to the concentrations (mM) indicated; Glc, 100; Gal, 100; Man, 50; rhamnose, 50; GlcNAc, 50; GalNAc, 50; lactose, 50; LNT,25. It should be emphasized that A. aurantia lectin was able to agglutinate Bombay phenotype cells, Oh Le(a+b-) (Iseki et al, 1970), although the reaction was weaker than with group O cells. The Oh cell lacks the H-determinant structure and fails to react with anti-H reagents.…”
Section: Resultsmentioning
confidence: 92%
“…These inhibiting patterns seem to be similar to those observed with eel serum and Lotus lectin (Watkins & Morgan, 1962), both of which are specific for fucose linked 1-*-2 to galactose (i.e., H-determinant structure). The following sugars failed to give significant inhibition when tested up to the concentrations (mM) indicated; Glc, 100; Gal, 100; Man, 50; rhamnose, 50; GlcNAc, 50; GalNAc, 50; lactose, 50; LNT,25. It should be emphasized that A. aurantia lectin was able to agglutinate Bombay phenotype cells, Oh Le(a+b-) (Iseki et al, 1970), although the reaction was weaker than with group O cells. The Oh cell lacks the H-determinant structure and fails to react with anti-H reagents.…”
Section: Resultsmentioning
confidence: 92%
“…Human O, A1; A2, B, AB and Oh red cells were used. Oh red cells, frozen in glycerol were supplied by the Department of Legal Medicine, School of Medicine, Gunma University [11], [12,13] was cultured in ordinary agar at 37 °C for 24 h, the cells were suspended in saline solution, and the suspension was incubated at 37 °C for 24 h with frequent shaking to disrupt them. The solution was centrifuged at a high speed, and the fraction obtained from the super natant at 30-60% ammonium sulfate saturation was used as a crude preparation of Hdecomposing enzyme.…”
Section: Methodsmentioning
confidence: 99%