Monoclonal antibody BR 96 and chemeric monoclonal antibodies having the variable region of MAB BR96 with bind to a variant of LEY antigen on human carcinoma cells

1997 ◽  
Vol 20 (6) ◽  
pp. 480
Blood ◽  
1983 ◽  
Vol 62 (5) ◽  
pp. 1022-1026 ◽  
Author(s):  
DL Urdal ◽  
TA Brentnall ◽  
ID Bernstein ◽  
SI Hakomori

Abstract 1G10, a monoclonal IgM antibody that identifies a differentiation antigen on human granulocytes and a subpopulation of monocytes, was found to react specifically with glycosphingolipids bearing the Gal beta 1–4(Fuc alpha 1–3)GlcNAc hapten (X determinant). This carbohydrate determinant was found on both glycolipid and glycoprotein molecules isolated from HL-60 cells (a promyelocytic leukemia cell line). Thus, this highly conserved carbohydrate-defined determinant previously described on mouse embryonic and mouse and human carcinoma cells is also expressed as a tissue-specific differentiation antigen on normal human granulocytes.


1985 ◽  
Vol 75 (5) ◽  
pp. 831-839 ◽  
Author(s):  
Silvana Canevari ◽  
Rosaria Orlandi ◽  
Marina Ripamonti ◽  
Elda Tagliabue ◽  
Salvatore Aguanno ◽  
...  

Blood ◽  
1983 ◽  
Vol 62 (5) ◽  
pp. 1022-1026
Author(s):  
DL Urdal ◽  
TA Brentnall ◽  
ID Bernstein ◽  
SI Hakomori

1G10, a monoclonal IgM antibody that identifies a differentiation antigen on human granulocytes and a subpopulation of monocytes, was found to react specifically with glycosphingolipids bearing the Gal beta 1–4(Fuc alpha 1–3)GlcNAc hapten (X determinant). This carbohydrate determinant was found on both glycolipid and glycoprotein molecules isolated from HL-60 cells (a promyelocytic leukemia cell line). Thus, this highly conserved carbohydrate-defined determinant previously described on mouse embryonic and mouse and human carcinoma cells is also expressed as a tissue-specific differentiation antigen on normal human granulocytes.


1989 ◽  
Vol 178 (3) ◽  
pp. 795-802 ◽  
Author(s):  
Francisco P. CONDE ◽  
Rosaria ORLANDI ◽  
Silvana CANEVARI ◽  
Delia MEZZANZANICA ◽  
Marina RIPAMONTI ◽  
...  

1984 ◽  
Vol 1 (4) ◽  
pp. 283-292 ◽  
Author(s):  
J.A. FORRESTER ◽  
D.P. McINTOSH ◽  
A.J. CUMBER ◽  
G.D. PARNELL ◽  
W.C.J. ROSS

2019 ◽  
Vol 34 (3) ◽  
pp. 147-159 ◽  
Author(s):  
Massimo Fantini ◽  
Justin M. David ◽  
Hing C. Wong ◽  
Christina M. Annunziata ◽  
Philip M. Arlen ◽  
...  

1994 ◽  
Vol 8 ◽  
pp. 54 ◽  
Author(s):  
R. Lopez-Alemany ◽  
F. Mirshahi ◽  
P. Burtin ◽  
C. Soria ◽  
N. Soria ◽  
...  

2016 ◽  
Vol 11 (03) ◽  
Author(s):  
L Berti ◽  
B Rädle ◽  
HU Häring ◽  
M Hrab((ebrevis)) de Angelis ◽  
H Staiger

2000 ◽  
Vol 41 (4-5) ◽  
pp. 301-308 ◽  
Author(s):  
N. Noda ◽  
H. Ikuta ◽  
Y. Ebie ◽  
A. Hirata ◽  
S. Tsuneda ◽  
...  

Fluorescent antibody technique by the monoclonal antibody method is very useful and helpful for the rapid quantification and in situ detection of the specific bacteria like nitrifiers in a mixed baxterial habitat such as a biofilm. In this study, twelve monoclonal antibodies against Nitrosomonas europaea (IFO14298) and sixteen against Nitrobacter winogradskyi (IFO14297) were raised from splenocytes of mice (BALB/c). It was found that these antibodies exhibited little cross reactivity against various kinds of heterotrophic bacteria. The direct cell count method using monoclonal antibodies could exactly detect and rapidly quantify N. europaea and N. winogradskyi. Moreover, the distribution of N. europaea and N. winogradskyi in a biofilm could be examined by in situ fluorescent antibody technique. It was shown that most of N. winogradskyi existed near the surface part and most of N. europaea existed at the inner part of the polyethylene glycol (PEG) gel pellet, which had entrapped activated sludge and used in a landfill leachate treatment reactor. It was suggested that this monoclonal antibody method was utilized for estimating and controlling the population of nitrifying bacteria as a quick and favorable tool.


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