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文献和实验to eliminate platelets. 5) Centrifuge at 350 x g for 20 minutes at 20°C. Allow to decellerate without brakes. 6) Recover MNC from the plasma/Lymphoprep interface and transfer the cells to a 50 ml tube. 7) Wash MNC
RAT/MOUSE GROWTH HORMONE ELISA KIT
of reading absorbency at 450 nm Orbital Microtiter Plate Shaker Absorbent Paper or Cloth 实验步骤 1. SAMPLE PREPARATION 1) No dilution or preparation is needed for normal serum or plasma samples. In the event
Isolation of Cell-Free RNA from Maternal Plasma
of cell-free RNA from plasma samples, and we have found the protocol using TRIzol LS reagent (Invitrogen) as lysis buffer combined with RNeasy Mini kit (QIAGEN) to be the optimal method for extracting high-quality cell-free RNA in the highest quantities
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