The invention discloses a method for extracting a large number of high-purity deoxyribonucleic acid (
DNA) from chicken blood. The method comprises absorbing an unfreezing chicken blood sample preserved through
DNA preserving fluid into a centrifugal tube containing a
reagent X; performing repeated dangling through a liquid-moving gun until the original blood sample becomes
clear liquid; performing
centrifugation and removing supernate; adding a
reagent Y, slightly performing suspension on centrifuged
sediment obtained by the last step; adding
ribonuclease (Rnase) A, evenly mixing and then performing warm bath at the temperature of 37 DEG C for 30 minutes; adding 5mol / L of
sodium perchlorate, performing manual oscillation to achieve mixing for 5 minutes; performing water bath, manually shaking the mixture for one time every 5 minutes; adding precooled
chloroform, mixing for 5 minutes, centrifuging and absorbing supernate into another centrifugal tube; adding isopyknic
isopropyl alcohol, and slowly shaking to obtain flocculent
DNA; washing the flocculent DNA through precooled 75% of
ethanol for two times, airing, performing
dissolution through appropriate TE (mixture of
tris and
ethylene diamine tetraacetic acid ), storing for one week at the temperature of 4 DEG C and then storing for a long term at the temperature of -20 DEG C. By means of the method, the time for extracting the DNA is short, the extracted DNA sample has high purity, large concentration and good quality, and the high-purity deoxyribonucleic acid (DNA) can completely meet requirements of downstream
molecular biology experiments.