Forward and reverse ABO typing and RhD blood type detecting card
A positive and negative stereotyping and detection card technology, applied in the medical field, can solve the problems of inability to effectively protect the stability of antibodies, the inability to balance sensitivity and specificity, and the inability to fully swell the gel, so as to ensure purity, ionic strength, The effect of ensuring stability
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Embodiment 1
[0032] A detection card for ABO positive and negative typing and RhD blood type, including a detection card containing six microcolumns, the first three microcolumns in the six microcolumns are equipped with equal amounts of anti-A gel, anti-B gel and anti-B gel respectively. Anti-D gel, and the remaining three microcolumns were filled with an equal amount of blank gel, which was prepared by the following method:
[0033] (1) Swelling of dextran gel:
[0034] Select Sephadex G-25, Sephadex G-50 and Sephadex G-75 to mix according to the mass ratio of 1:2:1 to obtain Sephadex mixture , and then add purified water according to the mass volume ratio of the dextran gel mixture and purified water as 1:3, and suspend and swell for 48 hours; then wash it with purified water three times to remove broken particles, and obtain uniform and complete Spherical curdlan gum particles;
[0035] (2) Preparation of antibody diluent:
[0036] Anti-A diluent: use physiological saline as the bas...
Embodiment 2
[0052] A detection card for ABO positive and negative typing and RhD blood type includes a detection card containing six microcolumns, and the first three microcolumns in the six microcolumns are equipped with equal amounts of anti-A gel, anti-B gel and anti-B gel respectively. Anti-D gel, and the remaining three microcolumns were filled with an equal amount of blank gel, which was prepared by the following method:
[0053] (1) Swelling of dextran gel:
[0054] Select Sephadex G-75 and Sephadex G-100 to mix according to the mass ratio of 1:1 to obtain Sephadex mixture, and then follow the method of Sephadex mixture and purified water Add purified water at a mass volume ratio of 1:2, suspend and swell for 72 hours; then wash it four times with purified water to remove broken particles, and obtain gelatin particles with uniform size and complete spherical shape;
[0055] (2) Preparation of antibody diluent:
[0056] Anti-A diluent: use physiological saline as the base fluid, w...
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