JoVE Encyclopedia of Experiments
Biological Techniques
0 views • 2:40 min • January 15th, 2026
Begin with human peripheral blood in a conical tube.
Centrifuge the tube at a low speed to separate the blood into three layers: red blood cells at the bottom, the buffy coat in the middle, and platelet-containing plasma at the top.
Transfer the plasma layer to a fresh tube and centrifuge it at a high speed to pellet the platelets.
Transfer the plasma supernatant to a new tube.
Collect the platelet pellet and reconstitute it with an appropriate volume of the plasma supernatant to obtain platelet-rich plasma or PRP, which contains a high concentration of platelets.
To begin, place the centrifugation tubes containing the anticoagulated blood in a clinical grade tabletop centrifugation machine set to room temperature within a sterile environment. Run the initial soft spin at 100 g for 15 minutes to separate the anticoagulated blood into three layers: red blood cells at the bottom, plasma on top, and the buffy coat in the middle.
Using an 18-gauge sterile spinal needle, pipette the top layer of plasma from the trilayer sample in a sterile manner. Collect the plasma into separate conical bottom centrifugation tubes, ensuring each tube holds 10 milliliters of plasma.
Then, place the 15-millil
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