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Reagents/Kits ABO Reagents Anti A (Monoclonal)
Reagents/Kits ABO Reagents Anti A (Monoclonal)
ABO Reagents
Anti A (Monoclonal)
In 1900, Landsteiner discovered the serum of some people would agglutinate the red cells of others. Four common phenotypes are now recognised: O, A, B and AB. Subgroups of A and B have since been identified.
The reagents will cause direct agglutination (clumping) of test red cells that carry the corresponding ABO antigen. No agglutination generally indicates absence of the corresponding ABO antigen
Lorne Monoclonal IgM ABO blood grouping reagents contain mouse monoclonal antibodies diluted in a phosphate buffer containing sodium chloride, EDTA and bovine albumin. Each reagent is supplied at optimal dilution for use with all the recommended techniques stated below without the need for further dilution or addition.
The reagents will cause direct agglutination (clumping) of test red cells that carry the corresponding ABO antigen. No agglutination generally indicates absence of the corresponding ABO antigen
Lorne Monoclonal IgM ABO blood grouping reagents contain mouse monoclonal antibodies diluted in a phosphate buffer containing sodium chloride, EDTA and bovine albumin. Each reagent is supplied at optimal dilution for use with all the recommended techniques stated below without the need for further dilution or addition.
Avaliable Sizes
5ml10ml
1000ml
5000ml
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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 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.
Anti H Lectin
The H antigen is part of the Hh system and is found on all red cells except those of Oh (hh) Bombay phenotype, which is extremely rare. H is the precursor of A and B and so group A and B people have less H than O people.
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 Lea (monoclonal)
The Lewis system antigens are not an integral part of the red cell membrane and are produced by tissue cells and found primarily in plasma and watery secretions. Red cells acquire Lewis antigens by absorption from surrounding plasma. The amount of Lewis antigen expressed on a cell can vary with the cell’s ABO phenotype. Anti-Lea and Anti-Leb have not been associated with Haemolytic Disease of the Newborn, but examples of Anti-Lea have caused Haemolytic Transfusion Reactions.
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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