[Book review] Fluorescent protein tracing: 4th edition, edited by R. Q. Nairn
Review of: Fluorescent protein tracing, 4th edition. 1976. R.C. Nairn. Edinburgh ; New York : Churchill Livingstone.
Geology topics
Publications and source records attributed to B.R. Griffin.
Review of: Fluorescent protein tracing, 4th edition. 1976. R.C. Nairn. Edinburgh ; New York : Churchill Livingstone.
A rainbow trout with a malignant lymphoma of probable thymic origin showed direct spread of the tumour to the gills, metastases to the liver and head kidney, and the presence of abnormal circulating lymphocytes. The cells of the tumour possessed plasma membrane immunoglobulin detectable by immuno–fluorescence. Examination of the tumour cells by transmission electron microscopy revealed no evidence of virus associated with the cells. Infectious viruses could not be detected in the tumour tissue, and the tumour was not transmissible by injection of live tumour cells into young rainbow trout. Attempts to establish the tumour in long–term culture were unsuccessful.
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Review of: Fish Immunology. Edited by M. J. Manning and M. F. Tatner. Academic Press, London. 1985. 374 pages. $32.50. Reviewed by B. R. Griffin, Fish Farming Experimental Station, U.S. Fish and Wildlife Service, Stuttgart, Arkansas 72160, USA.
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Three rabbit antisera raised to trout IgM showed positive immunofluorescent reactions with lymphocytes of trout spleen and thymus. These antisera showed no detectable cross-reactivity with keyhole limpet hemocyanin, as determined by direct radioimmune precipitation and adsorption, and did not appeare to react significantly with carbohydrate moieties on trout IgM, as determined by the failure of proteolytic digests of trout IgM to inhibit in radioimmunoassay against intact trout IgM. Membrane immunoglobulin determinants were detectable on the membrane of both thymocytes and splenocytes with the lactoperoxidase-catalyzed iodination reaction. Radioimmunoassay of lysates of lymphocytes confirmed the association of immunoglobulin with trout thymocytes. By radioimmunoassay, lysates of thymic and splenic lymphocytes contained similar amounts of immunoglobulin, equivalent to approximately 8 × 10 4 molecules of IgM per cell (calculated as the monomer µ 2 L 2 ).