Epoxy Nanocomposites with Carbon Nanotubes Produced by Floating Catalyst CVD.

Epoxy nanocomposites with float catalysis-produced CNT felt as a filler were prepared. Parameters such as the curing process, glass transition of epoxynanocomposites, structure and morphology of CNT felt, initial epoxy composition, and epoxy nanocomposites were investigated. The influence of CNT felt on curing process in epoxy nanocomposites with different amounts of curing agent was determined.

[Improving the efficacy of tuberculosis immunodiagnosis using anti-human IgG monoclonal antibodies].

Monoclonal antibodies (MAb) F5 to human IgG were used for creating immunoperoxidase conjugate. MAb dissociation constant was 10(-9)M-1 and the number of binding sites 1. Enzyme immunoassay (EIA) and immunoblotting showed that MAb F5 specifically recognize conformation epitope on intact human IgG molecule but not on other human immunoglobulins or denatured IgG.

[Serological and immunochemical properties of carbohydrate-containing fraction from mycobacterium tuberculosis H37Rv].

Using affinity chromatography on concanavalin A (Con A) sepharose CL 6B, a carbohydrate-containing fraction was derived from Mycobacterium tuberculosis H37Rv sonicate. Surprisingly, the main component of Con A fraction was a protein having a molecular weight of a 30-kD range which is generally absent in the Con A-adsorbed fraction from the culture filtrate. ELISA by means of an antimycobacterial monoclonal antibody panel showed that the 30-kD range of Con A fraction contained antigen 85.

[Comparative analysis of two mycobacterium tuberculosis antigens and two methodological approaches to determining serum antimycobacterial antibodies].

The glycoprotein (15-18 kDa) antigen of Mycobacterium tuberculosis H37Rv was affinity isolated on the immunosorbent with monoclonal antibodies S4C1G4 (specific to M. tuberculosis H37Rv; Avdiyenko V. G.

[Systematic approach to detection of anti-idiotypic antibodies to antimycobacterial idiotype in man and animals].

ELISA in the sandwich modification was developed to detect anti-idiotypic antibodies to the antituberculosis idiotype of monoclonal antibodies (MAb) S4C1G4 (anti 15-18 kDa H37Rv). Sera immunoglobulins were determined by Staphylococcus protein A capture. F[ab+]2, the MAb fragments S4C1G4 (IgG2a, kappa) and 1.