Separation and purification method and kit for fetal nucleated red blood cells
A technique for separating and purifying nuclear red blood cells, which is applied in the field of cell biology detection, can solve the problems of fetal cell enrichment, small number of separations, no substantive breakthroughs, limited range of diseases, etc., and achieve tolerance to separation and washing operations, The effect of avoiding a large amount of loss and improving the purity
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Embodiment 1
[0065] Embodiment 1: Separation and purification of fetal NRBC
[0066] Take 3ml of peripheral venous blood from pregnant women whose pregnancy is 16-18 weeks into heparin anticoagulant blood collection tubes, centrifuge at 500g for 5 minutes to remove plasma, and add 8ml of PBS (NaCl 137mmol / L, KCl 2.7mmol / L, NaCl 2.7mmol / L, NaCl 2 HPO 4 4.3mmol / L, KH 2 PO 4 1.4mmol / L, pH7.2) prepared 1% (w / v) NH 4 Cl solution, mix well, place in ice bath for 10 minutes, lyse red blood cells, centrifuge at 500g for 5 minutes to remove supernatant, shake the pellet to resuspend the cells. Then add 1ml of 3% glutaraldehyde solution prepared in PBS, and fix the cells for 10 minutes. Fully wash the cells twice with 10 ml of normal saline, resuspend the cells with 1 ml of normal saline, add 10E+8CD45 antibody-labeled magnetic beads (Miltenyl biotech, serial number 130-045-801), mix well for 15 minutes, and place on a magnetic separation rack Separate the cells, transfer the liquid part to a...
Embodiment 2
[0068] Take 3ml of peripheral venous blood from a pregnant woman whose pregnancy is 16-18 weeks into a heparin anticoagulant blood collection tube, centrifuge at 500g for 5 minutes to remove plasma, add 8ml of 1% NH prepared in PBS to the blood cell pellet 4 Cl solution, mix well, place in ice bath for 10 minutes, lyse red blood cells, centrifuge at 500g for 5 minutes to remove supernatant, shake the pellet to resuspend the cells. Then add 1ml of 3% glutaraldehyde solution prepared in PBS to fix the cells for 10 minutes. Fully wash the cells twice with 10 ml of normal saline, resuspend the cells with 1 ml of normal saline, add 10E+8CD45 antibody-labeled magnetic beads (Miltenyl biotech, serial number 130-045-801), mix well for 15 minutes, and place on a magnetic separation rack Separate the cells, transfer the liquid part to a test tube containing 10E+6CD71 antibody-labeled magnetic beads (Miltenyl biotech, serial number 130-046-201), mix well for 15 minutes, separate the cell...
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