A kind of anti-sieve cell suitable for platelet antibody detection, its preparation method and application
An antibody detection and platelet technology, applied in cell dissociation methods, biochemical equipment and methods, blood/immune system cells, etc., can solve the problems of increased difficulty, high price and high detection cost of platelet antibody detection, and achieve the effect of antigen preservation. Good, long storage time, easy to use effect
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Embodiment 1
[0036] Embodiment 1, preparation anti-sieve cell
[0037] 1) Mix equal volumes of O-type platelets for 3 persons that have been screened to confirm the antigen profile, wash 3 times with platelet cleaning solution, centrifuge after each wash, discard the supernatant after each centrifugation, and retain the platelet precipitate;
[0038] 2) Use platelet loading solution to resuspend the platelet pellet in step 1) and adjust the cell concentration to 1.5×10 10 cells / ml, shaking at 37°C for 2 hours;
[0039] 3) After shaking, use platelet cleaning solution to wash 2 times. After cleaning, use platelet storage solution to resuspend the pellet and adjust the cell concentration to 3.0×10 7 cells / ml to obtain anti-sieve cells suitable for platelet antibody detection.
[0040] Wherein, the platelet cleaning solution includes: sodium citrate 10mmol / L, sodium chloride 77mmol / L, potassium chloride 15mmol / L, sodium dihydrogen phosphate 20mmol / L, sodium acetate 15mmol / L, magnesium chlor...
Embodiment 2
[0043] Embodiment 2, preparation anti-sieve cell
[0044] 1) Mix equal volumes of O-type platelets for 3 persons that have been screened to confirm the antigen profile, wash 3 times with platelet cleaning solution, centrifuge after each wash, discard the supernatant after each centrifugation, and retain the platelet precipitate;
[0045] 2) Use platelet loading solution to resuspend the platelet pellet in step 1) and adjust the cell concentration to 1.0×10 10 cells / ml, shaking at 37°C for 2 hours;
[0046] 3) After shaking, use platelet cleaning solution to wash 2 times. After cleaning, use platelet storage solution to resuspend the pellet and adjust the cell concentration to 2.0×10 7 cells / ml to obtain anti-sieve cells suitable for platelet antibody detection.
[0047] Wherein, the platelet cleaning solution includes: sodium citrate 10mmol / L, sodium chloride 77mmol / L, potassium chloride 15mmol / L, sodium dihydrogen phosphate 20mmol / L, sodium acetate 15mmol / L, magnesium chlor...
Embodiment 3
[0050] Embodiment 3, preparation anti-sieve cell
[0051] 1) Mix equal volumes of O-type platelets for 3 persons that have been screened to confirm the antigen profile, wash 3 times with platelet cleaning solution, centrifuge after each wash, discard the supernatant after each centrifugation, and retain the platelet precipitate;
[0052] 2) Use platelet loading solution to resuspend the platelet pellet in step 1) and adjust the cell concentration to 2.0×10 10 cells / ml, shaking at 37°C for 2 hours;
[0053] 3) After shaking, use platelet cleaning solution to wash 2 times. After cleaning, use platelet storage solution to resuspend the pellet and adjust the cell concentration to 5.0×10 7 cells / ml to obtain anti-sieve cells suitable for platelet antibody detection.
[0054] Wherein, the platelet cleaning solution includes: sodium citrate 10mmol / L, sodium chloride 77mmol / L, potassium chloride 15mmol / L, sodium dihydrogen phosphate 20mmol / L, sodium acetate 15mmol / L, magnesium chlor...
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