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. 2017 Jan 3;2017:7404912. doi: 10.1155/2017/7404912

Table 1.

Human blood fractions obtained in the investigation.

Blood fraction Description Method of isolation Characteristics of the method
(I) cells Whole blood, enriched with blood cells 1,200g, pellet Preparation of platelet-poor plasma [19] and estimation of haemolysis [20]
(II) plasma Platelet-poor blood plasma 1,200g, supernatant
(III) 16,000g plasma pellets Intermediate fraction containing membrane vesicles and cell debris 16,000g, pellet Isolation of microvesicles [21]
(IV) 160,000g plasma pellets Fraction enriched with exosomes 160,000g∗∗, pellet High-recovery isolation of exosomes [22]
(V) 160,000g plasma supernatant Vesicle-depleted plasma 160,000g∗∗, supernatant

Centrifugation for 20 min at 4°C.

∗∗Centrifugation for 120 min at 4°C.