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Reagents/Kits Precise Anti-D Precise Anti-D - 209
Reagents/Kits Precise Anti-D Precise Anti-D - 209
Precise Anti-D
Precise Anti-D - 209
Careful control of both manual and automated techniques for detecting antibodies is essential. Testing of a weak IgG Anti-D with group O R1r red cells in parallel with routine antiglobulin or enzyme tests will confirm the efficacy or otherwise of the chosen technique.
When used by the recommended techniques, the reagent will cause agglutination (clumping) of red cells carrying Rh D antigen. No agglutination when tested against Rh D positive red cells usually indicates a problem with the anti-human globulin or enzyme test
Lorne Precise Weak Anti-D Control Reagent is prepared from pools of human serum containing low activity Anti-D. The pool is diluted in inert serum to give a final concentration of 0.10 IU/ml Anti-D. ABO antibodies are not absorbed. The reagent is supplied at the optimal dilution, for use with all the recommended techniques stated below without the need for further dilution or addition
When used by the recommended techniques, the reagent will cause agglutination (clumping) of red cells carrying Rh D antigen. No agglutination when tested against Rh D positive red cells usually indicates a problem with the anti-human globulin or enzyme test
Lorne Precise Weak Anti-D Control Reagent is prepared from pools of human serum containing low activity Anti-D. The pool is diluted in inert serum to give a final concentration of 0.10 IU/ml Anti-D. ABO antibodies are not absorbed. The reagent is supplied at the optimal dilution, for use with all the recommended techniques stated below without the need for further dilution or addition
Avaliable Sizes
5ml - 2090051000ml - 209000
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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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