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The hippocampi were dissected free and 400 µm-thick (transverse section in hippocampus) slices were cut using a tissue chopper.
Brains obtained from E39-E40 embryos were cut under sterile conditions into 400 µm thick coronal slices using a tissue chopper (Stoelting, Wood Dale, IL).
Briefly, 350 µm thick hippocampal slices were prepared from postnatal 8-day-old (PND-8) Wistar rats using a tissue chopper and separated in ice-cold Hank's balanced salt solution (HBSS) with 33.3 mM glucose, 4.2 mM NaHPO4, 10 mM MgSO4, 10 mM HEPES, 0.3% BSA and Penicillin-Streptomycin, pH 7.3.
Then transverse sections (400 μm) were obtained using a tissue chopper.
Coronal slices (∼300 μm) were then prepared using a tissue chopper and trimmed to ∼10 mm slices containing both nuclei.
In the present study, we isolated the forebrain from early postnatal mice and sectioned them sagittally into 350-μm-thick slices by using a tissue chopper.
Similar(47)
Without using a tissue.
Pat dry lightly using a tissue.
Briefly, tissues were washed, dissected, automatically sectioned using a McIlwain tissue chopper (Campden Instruments, Loughborough, England) and cut into 500-μm pieces in DMEM 10% FCS, and plated on glass coverslips (12-mm diameter) precoated with poly-(L -lysine (10 μg/mL -lysineAldrich).
Cultures were passaged weekly using a McIlwain tissue chopper.
Hippocampi were dissected and cut into 250 µm thick slices using a McIlwan Tissue Chopper.
More suggestions(15)
using a tissue phantom
using a tissue grinder
using a tissue engineering
using a tissue chamber
using a tissue microarray
using a tissue gram
using a paper chopper
using a tissue protocol
using a tissue array
using a tissue expression
using a fodder chopper
using a tissue protector
using a tissue cylinder
using a tissue cage
using a tissue adhesive
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