This study demonstrates the potential quality of a
flow cytometric technique to live protoplasm survival time in cats utilizing
autologous platelets tagged in vitro with fluorescein isocyanate (FITC). when put next with a 51Cr technique, no vital
variations in calculable survival times were found.
Each the 51Cr and FITC‐labelling
procedures evoked similar changes in protoplasm form and collagen‐induced
aggregation.
Platelets tagged with FITC had considerably larger
volumes compared with those of glutaraldehyde‐fixed platelets. These changes
were primarily associated with the protoplasm natural action and laundry
procedures instead of the labels themselves. This novel technique probably has
wide pertinence to cell circulation time studies as flow cytometry
instrumentality becomes a lot of promptly on the market.
In a preliminary study of the protoplasm survival time
in feline cancer of the blood virus (FeLV)‐infected cats, 2 of 3 cats had
considerably reduced survival times exploitation each flow cytometric and radio-isotopic
strategies. These information recommend enlarged protoplasm turnover in
FeLV‐infected cats.
To Know More: Join us in the Discussion: 8th European
Clinical Microbiology and Immunology Congress on June 12-13, 2019, Edinburgh,
Scotland
Contact: Erika Madison
Office Phone: 44 203 769 1755
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