Composition and kit for rapid extraction of circulating unrelated nucleated cell from peripheral blood and application thereof
A composition and kit technology, applied in the fields of biochemical equipment and methods, microorganisms, tissue culture, etc., can solve the problems of inconvenient application, low leukocyte removal rate, long time consumption, etc., to simplify operation, shorten centrifugation time, and improve efficiency. Effect
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Embodiment 1
[0055] Utilizing the composition of the present invention to rapidly obtain non-blood circulating nucleated cells from human blood samples
[0056] Collect 10ml of human peripheral blood into any blood collection tube (BD, New Jersey, USA) containing anticoagulant (such as EDTA, heparin, or ACD, etc.). After centrifugation (1000 xg, 15 minutes), plasma proteins were removed.
[0057] After adding 50 ml of hypotonic erythrocyte thawing solution (BD Pharmingen, California, USA), incubate at 4° C. for 30 minutes. The sample specimen was centrifuged again (1000 xg, 15 minutes).
[0058] Resuspend the pelleted cells in 30 mL of buffer. 2 ml of magnetic beads coated with anti-CD45 and / or CD50 monoclonal antibodies (Invitrogen, California, USA) were added thereto, and incubated at room temperature for 30 minutes. The reaction solution is added above the cell separation medium of 20 ml (the specific gravity of the cell separation medium at 20° C. is 1.07260 to 1.07650 g / ml, and the...
Embodiment 2
[0082] Using the kit of the present invention to rapidly obtain non-blood circulating nucleated cells from human blood samples
[0083] Collect 10ml of human peripheral blood into the blood collection tubes carried in the kit containing any of the following anticoagulants, such as EDTA, heparin, or ACD. After centrifugation (1000 xg, 15 minutes), plasma proteins were removed.
[0084] After adding 50 ml of hypotonic erythrocyte thawing solution (BDPharmingen, California, USA) carried in the kit, incubate at 4° C. for 30 minutes. The sample specimen was centrifuged again (1000 xg, 15 minutes).
[0085] Resuspend the deposited cells in 30 mL of the buffer provided in the kit. 2 ml of magnetic beads coated with anti-CD45 and / or CD50 monoclonal antibodies (Invitrogen, California, USA) carried in the kit were added thereto, and incubated at room temperature for 30 minutes. Add the reaction solution above the 20 ml of cell separation medium carried in the kit (the specific gravit...
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