Method for separating and authenticating erythroblast of blood
A technology for nucleating red blood cells and blood, applied in the field of blood separation, identification and detection, can solve the problems of easy pollution, complicated operation and high cost
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[0090] (1) Preparation of main reagents
[0091] 1. Polylysine working solution: fully mix polylysine stock solution with double distilled water 1:10, and wait for the bubbles to disappear for later use;
[0092] 2. 0.01mol / L PBS (PH7.4) containing 0.5% BSA
[0094] Na 2 HPO 4 12H 2 O 4g
[0095] NaH 2 PO 4 2H 2 O 0.35g
[0096] Add 800ml of double distilled water, adjust the pH value to 7.4, and make up to 1000ml with double distilled water. 0.01mol / L PBS, after autoclaving, add 5g BSA, store at 40°C.
[0097] 3. Alkaline cell lysate (containing KOH 200mmol / L, DTT 50mmol / L)
[0098] 400mmol / L KOH 1ml
[0099] 1mol / L DTT 100ul
[0100] Sterile water for injection is 850-900ul, mixed thoroughly, filtered through a 0.22μm microporous filter, subpackaged, and stored at -20°C for later use.
[0101] (2) Anti-degumming slide preparation
[0102] 1. Pretreatment of slides
[0103] Wash the ordinary glass slide with hot soapy water, clean...
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