Vet Immunol Immunopathol
September 1994
In an attempt to improve the accuracy of sexing bovine embryos, new anti-H-Y monoclonal antibodies were produced and selected, using an extended screening procedure. In addition to the commonly used screening of soluble H-Y antigen sources, such as testis supernatant and Daudi supernatant, the binding specificity to cell surface H-Y antigen was tested also. A radioimmunoassay (RIA) employing male and, as a control, female bovine lymphocytes, and enzyme-linked immunosorbent assays (ELISAs) on solubilized membrane fractions resulted in the selection of a number of clones producing monoclonal antibody (mAb) with male-enhanced binding.
View Article and Find Full Text PDFIn vitro cultures of intact chick gonads (organ cultures) and reaggregation cultures of dispersed gonad cells (roller cultures) were made. Gonads or gonad cells from 7-day-old chick embryos, at the stage when sex-specific differentiation begins, were cultured in the presence of presumed H-Y antigen-containing supernatants, or co-cultured in the presence of H-Y antigen-producing cell lines. The H-Y antigen-producing cells tested were of human, mouse, bovine and chicken origin.
View Article and Find Full Text PDFPost-weaning anoestrus was studied in eighteen primiparous sows, selected from a breed showing a high proportion of anoestrous sows. The sows were studied from late lactation, through weaning at day 29 post-partum (p.p.
View Article and Find Full Text PDFVet Immunol Immunopathol
November 1992
In the present experiments the efficacy of murine and bovine monoclonal antibodies for passive immunization in cattle was compared. The in vivo immunoneutralization of pregnant mare serum gonadotrophin (PMSG) by murine and bovine antibodies after repeated administration was chosen as a model for this study. Results indicate that repeated injections of murine monoclonal antibodies against PMSG (mMCA) alone did not, or only to a small extent, elicit an anti-mouse immune response.
View Article and Find Full Text PDFBovine-murine heteromyeloma cell lines were prepared by fusing lymphoid cells from a bovine leukemia virus (BLV)-infected cow with mouse myeloma cells. Selection of hybrid cell colonies was based on the ratio of bovine and murine chromosomes, the presence of cell-surface immunoglobulins and growth characteristics. First-generation fusion partners were compared for fusion efficiency and the number of antigen-specific antibody-producing clones generated.
View Article and Find Full Text PDFMonoclonal antibodies against the H-Y antigen were produced using spleen cells from female C57BL/6 mice hyperimmunized with cells from syngeneic males. Anti-H-Y positive clones were detected by enzyme immunoassays. Supernatant fluids from Daudi cell cultures and testicular cell preparations taken from mice, rabbits or calves served as presumptive sources of H-Y antigen.
View Article and Find Full Text PDFThe hybridoma technology for production of monoclonal antibodies circumvents many of the constraints associated with the use of conventional antisera, and consequently broadens the areas of application of antibodies in animal sciences. In the present review, the potential usefulness of monoclonal antibodies in animal production - with emphasis on reproduction - is discussed, including the inherent limitations of the current technology and the improvements that can be foreseen within the next few years. Because of their unique specificity and the fact that they can be produced in virtually unlimited quantities, monoclonal antibodies are an important tool in diagnostics.
View Article and Find Full Text PDFDiagnostics in animal production is an important field for application of monoclonal antibodies (MCAs). Representative examples are discussed. MCAs can also be used to influence physiological processes with regard to optimization of growth, reproduction, etc.
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