Characterization of immobilized antibodies on silica surfaces

1988 ◽  
Vol 35 (6) ◽  
pp. 466-471 ◽  
Author(s):  
Jinn-Nan Lin ◽  
J. Herron ◽  
J.D. Andrade ◽  
M. Brizgys
1981 ◽  
Vol 218 ◽  
pp. 395-407 ◽  
Author(s):  
Heinz Engelhardt ◽  
Hartmut Müller

1980 ◽  
Vol 29 (3) ◽  
pp. 999-1006 ◽  
Author(s):  
M W Russell ◽  
E D Zanders ◽  
L A Bergmeier ◽  
T Lehner

An antigenic component (antigen I) of the cell surface of Streptococcus mutans has been purified from culture supernatants and shown to be immunologically identical to the protease-susceptible moiety of antigen I/II. Ion-exchange and gel filtration chromatography failed to yield a physicochemically homogeneous product. Immunoasbsorbent chromatography on single and tandem columns containing immobilized antibodies to antigens I/II and II yielded identical products which were homogeneous in sodium dodecyl sulfate-polyacrylamide gel electrophoresis, and which when injected into rabbits induced monospecific antisera to antigen I. This antigen consisted of approximately 70% protein. Its molecular weight was estimated as 150,000, and the isoelectric point was estimated to be 5.1. Immunofluorescence microscopy using monospecific antiserum to antigen I showed that a similar antigen was present on cells of S. mutans serotypes a, c, d, e, f, and g, but not b.


2002 ◽  
Vol 5 (1) ◽  
pp. 67-77 ◽  
Author(s):  
George R. Newkome ◽  
Kyung Soo Yoo ◽  
Charles N. Moorefield

2007 ◽  
Vol 1007 ◽  
Author(s):  
Christian Bonhomme ◽  
Sophie De Monredon ◽  
François Ribot ◽  
Florence Babonneau

ABSTRACTDespite the huge amount of experimental investigations dedicated to the grafting of organoalkoxysilanes on silica, the characterization of covalent linkages remains a difficult task from a spectroscopic point of view. In most cases, the formation of a covalent link is taken for granted and not discussed. 29Si NMR, IR or UV spectroscopies are commonly used to study the modification of silica surface. Herein we report an unambiguous method to evidence the formation of covalent links. It is based on NMR spectroscopy analysis coupled with a rigorous synthetic grafting protocol.


1977 ◽  
Vol 67 (1) ◽  
pp. 251-268 ◽  
Author(s):  
Burkhard E Wagner ◽  
John N Helbert ◽  
Edward H Poindexter ◽  
Richard D Bates

1988 ◽  
Vol 127 ◽  
Author(s):  
J.-C. Petit ◽  
J.-C. Dran ◽  
L. Trotignon ◽  
J.-M. Casabonne ◽  
A. Paccagnella ◽  
...  

ABSTRACTWe have investigated the relationship between hydrated layer formation during aqueous corrosion of silicates and retention of heavy elements (Fe, REE, actinides). Our approach is based on the comparison of the dissolution behaviour of silicate glasses, silicate minerals implanted with increasing doses of lead ions (1×E+12 to 1×E+15 ions/cm2), sorption experiments on silica surfaces and direct precipitation of hydrosilicates. The characterization of reacted surfaces was performed by combining Rutherford backscattering spectrometry (RBS) for profiling heavy elements with Resonant Nuclear Reaction Analysis (RNRA) for hydrogen profilimetry. The accumulation of these elements does not necessarily imply a selective dissolution and can be explained by the “precipitation” of hydroxides or hydrosilicates.


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