1972
DOI: 10.4269/ajtmh.1972.21.868
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Use of Stable Sensitized Cells in Indirect Microhemagglutination Test for Malaria *

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Cited by 18 publications
(9 citation statements)
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“…The method was modified from that of Farshy and Kagan (1972). A reaction mixture of the following substances, added in the order given, was prepared and subsequently kept in the cold: 1.7% NaC1, 12 ml; 40% v/v aqueous pyruvic aldehyde, 4 ml; 1.0% Na2C03, 35 ml; Sorensen's phosphate buffer (PH 7.2) 7 ml.…”
Section: Sheep Red Blood Cells (Srbcmentioning
confidence: 99%
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“…The method was modified from that of Farshy and Kagan (1972). A reaction mixture of the following substances, added in the order given, was prepared and subsequently kept in the cold: 1.7% NaC1, 12 ml; 40% v/v aqueous pyruvic aldehyde, 4 ml; 1.0% Na2C03, 35 ml; Sorensen's phosphate buffer (PH 7.2) 7 ml.…”
Section: Sheep Red Blood Cells (Srbcmentioning
confidence: 99%
“…The cells were then washed thrice in PBS and stored in this as a 2.5% v/v suspension at 4°C. Double-aldehyde stabilisation ( D A S ) was performed as described by Farshy and Kagan (1972). The cells were first stabilised with pyruvic aldehyde (as above).…”
Section: Sheep Red Blood Cells (Srbcmentioning
confidence: 99%
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“…In the diagnosis of some infectious diseases as extraintestinal ame biasis, schistosomiasis, malaria, Pseudomonas infection or hepatitis [4][5][6][7]17], stable sensitized red blood cells have been used successfully in a standardized indirect hemagglutination test. Therefore, it was tried to develop a similar technique for the detection of antibodies against horse globulin and to compare the sensitivity and specificity of this test with the conventional indirect hemagglutination tests using fresh red blood cells as well as with other immunological methods.…”
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confidence: 99%