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The cell pellets were re-suspended at 10 cells per 500 μl of the same buffer and poured into the column reservoir.
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The constituents of the production medium were dissolved in the buffer solution and poured into the flask contained 50 mL of the buffered medium at the particular pH.
Bacteria (4 × 10) were added to 10 ml 1% LMP agarose (Invitrogen) containing 1% Todd Hewitt broth, 10 mM phosphate buffer, pH 7.4 and poured into a square Petri dish.
The resins were recovered by centrifugation, resuspended in buffer A containing 5 mM imidazole, and poured into columns.
Briefly, 20 mg of PLGA-PCL was dissolved in an appropriate amount of dichloromethane and poured into 100 μL of phosphate buffer saline (PBS; pH 7.4) as the inner aqueous phase (W1) containing MMP-1.
The mixture was cooled and poured into ice-cold water.
Drain and pour into a casserole dish.
Mix and pour into a container.
Blend it and pour into drinking glasses.
Take infuser out and pour into cups.
borax and pour into the bottle.
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CEO of Professional Science Editing for Scientists @ prosciediting.com