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Reagents / Kits Potentiator For Blood Screening L.I.S.S Concentrate
Reagents / Kits Potentiator For Blood Screening L.I.S.S Concentrate
Potentiator For Blood Screening
L.I.S.S Concentrate
Reducing the ionic strength of a test system increases the rate of red blood cell antigen-antibody binding. Low and Messeter in 1974 showed that the use of a low ionic strength solution enhances the rate of antibody uptake in first stage of agglutination, allowing incubation times to be shortened.
When used by the recommended techniques, the solution will reduce the ionic-strength of a test system, increase the rate of red blood cell antigen-antibody binding and permits a substantial reduction in incubation time and an increases in the test sensitivity with many antibody specificities
Lorne LISS Concentrate is a solution of glycine, phosphate buffer and 0.3 M sodium chloride. The solution is supplied at a stronger concentration than needed for serological use. It must be diluted 10 times in deionised water before being used with all recommended techniques mentioned.
When used by the recommended techniques, the solution will reduce the ionic-strength of a test system, increase the rate of red blood cell antigen-antibody binding and permits a substantial reduction in incubation time and an increases in the test sensitivity with many antibody specificities
Lorne LISS Concentrate is a solution of glycine, phosphate buffer and 0.3 M sodium chloride. The solution is supplied at a stronger concentration than needed for serological use. It must be diluted 10 times in deionised water before being used with all recommended techniques mentioned.
Avaliable Sizes
500ml2500ml
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Toxoplasmosis Latex Test Kit - 033
When used by the recommended techniques, latex particles in the reagent will agglutinate (clump) in the presence of Toxoplasma gondii antibodies. No agglutination generally indicates absence of the Toxoplasma antibody
Anti Jka - 323
The Jka and Jkb antigens were reported in 1951 and 1953 respectively. Anti-Jka and anti-Jkb can both show dosage and are notorious for their evanescence: antibody titres that rise after stimulation but quickly drop, often to undetectable levels. Kidd system antibodies have been implicated in delayed and immediate Haemolytic Transfusion Reactions and Haemolytic Disease of the Newborn.
Coombs Control Cells - 970
In 1945, Coombs, Mourant and Race described the use of anti-human globulin serum for detection of red cell-bound non-agglutinating antibodies and the antiglobulin (Coombs) test was rapidly applied. One cause of false negative antiglobulin tests is improper washing of the cells which results in free globulin molecules being present with supposedly washed cells and these globulins neutralise the antiglobulin serum when it is added. A negative result in an antiglobulin test should only occur when anti-human globulin is added to red cells that are not sensitised. To show that test cells were properly washed and that no neutralisation has occurred, antibody-coated cells are used as a positive indicator.
Anti CW Silde - 216
Levine and Stetson discovered the Rh blood group system in 1940. Apart from D the other major Rh antigens are C, E, c and e. The D antigen is highly immunogenic and the C and e antigens are less immunogenic than E and c. The Cw antigen is one of the more rare antigens, but Anti-Cw is a fairly commonly encountered antibody. All the Rh antibodies are clinically significant since they may cause both Transfusion Reactions and Haemolytic Disease of the Newborn.
Monoclonal Anti Fya - 774
The Fya and Fyb antigens were reported in 1950 and 1951 respectively. Anti-Fya and anti-Fyb have both been implicated in immediate and delayed Haemolytic Transfusion Reactions and Haemolytic Disease of the Newborn.
Avaliable Sizes
If you would like A different size to the ones we have listed, please contact us with your requirement.info@lornelabs.com
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