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The subcutaneous tissue was separated from the deep fascia on the ulnar and radial sides of the incision.
Decidual tissue was separated from specimens obtained by suction evacuation of the uterus.
The subcutaneous fat tissue was separated from abdominal skin and it was minced with a scalpel blade into smaller pieces.
Cortical tissue was separated from the medullary portion of each kidney under magnification with a dissecting microscope and suspended in 20 fold excess (wt/vol) of TRIzol® reagent (Invitrogen, Carlsbad, CA).
Immediately after surgery, thymus tissue was separated from the fibrotic capsule and from visible blood-vessels, mechanically disaggregated using a scalpel and scissors followed by pipetting several times with phosphate buffered saline (PBS).
Coral tissue was separated from the coral skeleton with a modified airgun attached to a SCUBA cylinder and subsequently stored in 20% DMSO preservation buffer and kept at −20°C until further processing.
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The protein tissue is separated from the liquid phase in a desludging type of centrifuge, following which a second centrifuge separates the fat from the aqueous protein layer.
The light emitted back from the tissue is separated from the excitation light and the focal point is imaged onto a pinhole in front of the detection system.
After lipoaspirate collection, the adipose tissue is separated from the tumescent solution, oil, serum, cell debris, and blood by centrifugation.
Ovaries were dissected and follicular fluid, cumulus cells, oocytes and interstitial tissue were separated from each other prior to total RNA extraction.
With blunt Wescott scissors using the two cuts for access, the episcleral tissue is separated from the muscle sheath and the sclera (fig 1H).
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