Preparation method of ABO/RhD blood typing detection reagent card
A technology for detecting reagents and reagent cards, applied in the field of blood transfusion medicine, can solve the problems of wrong ABO blood group, large gaps in the gel, large particles, etc., and achieve the effect of ensuring ionic strength and strong buffering capacity
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Embodiment 1
[0042]Step 1, preparation of gel suspension medium
[0043] Described gel suspending medium formula is as follows:
[0044] Methylparaben (5.5-6.5)×10 -4 g / ml
[0045] Propylparaben (1.0-1.5)×10 -4 g / ml
[0046] Glycine (1.6-1.9)×10 -2 g / ml
[0047] Sodium chloride (1.7-1.8)×10 -3 g / ml
[0048] Potassium dihydrogen phosphate (2.1-2.4)×10 -4 g / ml
[0049] Disodium hydrogen phosphate (4.6-4.8)×10 -4 g / ml
[0050] Bovine serum albumin ≤4%,
[0051] Dissolve the above reagents in distilled water and adjust the pH value to 6.6-6.8.
[0052] Step 2. Preparation of the gel
[0053] Polyacrylamide dextran gel is selected, and the particle size is 30-60 nanometers.
[0054] Soak in the gel suspension medium prepared in step 1, then wash with the gel suspension medium for 3-5 times, remove the broken fragments of the gel and the aggregated gel particles, and collect the applicable gelatin powder with uniform particle size and complete spherical shape. gel.
[0055] Step ...
Embodiment 2
[0076] The method of using the ABO / RhD blood typing detection reagent card is as follows:
[0077] 1. The ABO / RhD blood typing test reagent card has six gel tubes. The first tube is anti-A gel, the second tube is anti-B gel, the third tube is anti-D gel, and the fourth to sixth tubes are blank gels (gels containing gel suspension medium). The fourth and fifth tubes are respectively added with the serum (syrup) to be tested and tested with type A and type B reagent red blood cells. The sixth tube is a negative control tube.
[0078] 2. Use LISS solution or physiological saline to prepare the red blood cells of the subject to be tested to a concentration of 0.8-1% (weight percentage), and add them to the first, second, third and sixth microtubes respectively, 50 μl in each tube.
[0079] 3. Adjust known type A and type B erythrocytes with LISS solution or normal saline to a concentration of 0.8-1% (weight percentage), and add them to the fourth and fifth microtubes respectivel...
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