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The total haemocyte count was determined directly using a Neubauer chamber.
Functional and molecular immune response of Mediterranean mussel (Mytilus galloprovincialis) haemocytes against pathogen-associated molecular patterns and bacteria.
Effects of air exposure on the lysosomal membrane stability of haemocytes in blacklip abalone, Haliotis rubra (Leach).
Characterisation of monoclonal antibodies to haemocyte types of scallop (Chlamys farreri).
Measurement of reactive oxygen intermediate production in haemocyte of the penaid shrimp (Penaeus vannamei).
Flow cytometric analysis of haemocytes from eastern oysters, Crassostrea virginica, subjected to a sudden temperature elevation II: haemocyte functions: aggregation, viability, phagocytosis, and respiratory burst.
Conversion of phenoloxidase and peroxidase indicators in individual haemocytes of Mytilus edulis specimens and isolation of phenoloxidase from haemocyte extract.
of cooling and emersion on total haemocyte count and phenoloxidase activity of the spiny lobster Panulirus interruptus.
Enzyme characterisation of the circulating haemocytes of the carpet shell clam Ruditapes decussatus (Mollusca: bivalvia).
The direction of these changes depends on the typological peculiarities of the organism, haemocytes features, initial level of indices [8, 9, 10, 11, 12].
In a previous study, D-NAME, even though it had been widely used as an inactive isomer of the NOS inhibitor, was able to inhibit laminarin-stimulated NO production in primary haemocytes from the snail Lymnaea stagnalis (Wright et al.
The haemolymph was centrifuged at 5000 rpm for 10 min to remove haemocytes and debris and the supernatant was collected and used.
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