Chemiluminescence ELISA for the detection of antibodies to bovine leukaemia virus antigens.

A chemiluminescence enzyme-linked immunosorbent assay (ELISA) for the detection of antibodies to bovine leukaemia virus antigens (BLV) has been developed. The possibility of using an enhanced chemiluminescence reaction for the determination of adsorbed immunoperoxidase conjugates was studied in this work. The intensity of chemiluminescence depends on both the concentration of reagents and experimental conditions used.

[The determination of microalbuminuria by immunoenzyme analysis].

The authors have defined the optimal conditions for inhibitory type enzyme immunoassay of microalbuminuria. The range of albumin detection is 30 to 250 micrograms/ml. The optimal time of antigen binding with antibody is 45 min, the lower threshold level of albumin detection 0.

[The comparative evaluation of spectrophotometric and chemiluminescent detection in an immunoenzyme test of antibodies to the antigens of the bovine leukosis virus].

Comparative evaluation of the sensitivity limit in the detection of antibodies to bovine leukemia virus in the enzyme immunoassay with the use of chemiluminescent and spectrophotometric detection techniques was carried out. In this assay 3-amino-1,4-phthalazinedion was used as chemiluminescent substrate and ortho-phenylenediamine, as chromogenic substrate. The chemiluminescent signal was registered by means of a special luminometer designed at the Institute of Biochemistry (Lithuanian Acad.

Quantitative binding of Fc-receptors, and antibody-dependent cell-mediated cytotoxicity of blood lymphocytes in healthy and chronic lymphocytic leukemic cattle.

The binding capacity of Fc-receptors for IgG of blood lymphocytes was studied in healthy cattle and cattle with chronic lymphocytic leukemia before and after incubation at 37 degrees C in basal Eagle's medium without serum. It was found that lymphocytes of leukemic cattle possess twice the amount of Fc-receptors found in normal lymphocytes. The changes in the binding capacity of Fc-receptors for IgG of normal and leukemic lymphocytes correlated with those of antibody-dependent cell-mediated cytotoxicity (ADCC) of the corresponding lymphocytes.