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Band saw

Manufactured by EXAKT
Sourced in Germany

The EXAKT Band Saw is a precision cutting instrument designed for accurate and controlled sectioning of materials. It features a continuous loop of sharp steel teeth mounted on a sturdy frame that allows for smooth, straight cuts.

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8 protocols using band saw

1

Harvesting and Analyzing Stented Arteries

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Stented arterial segments were harvested after 4 weeks for quantitative analysis (3 groups, n = 10 per group), or after 1 week (2 groups, n = 2 per group) for qualitative analysis with SEM. Segments harvested 4 weeks after implantation were fixed under pressure with 4% formaldehyde, fixed overnight in 4% formaldehyde after excision, and stored in 70% ethanol. The segments were dehydrated in a graded series of acetone and embedded in resin (methyl methacrylate and butyl methacrylate, 1:1). Sections (7μm) were cut with a rotary microtome (Leica) from the middle of the stent, after sawing the segment with a band saw (Exakt). Segments harvested after 1 week were fixed in a mixture of 1% (wt/vol) glutaraldehyde and 4% (wt/vol) formaldehyde in 100mmol/L sodium cacodylate buffer (pH 7.4) and incubated at 4°C. Stent were cut longitudinally for en face imaging. After dehydration in a graded series of ethanol followed by hexamethyldisilazane, segments were sputtered with a gold layer.
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2

Histological Assessment of Bone Regeneration

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Bone regeneration was assessed via non-decalcified histology.25 (link) After formalin fixation,
samples were dehydrated with gradients of ethanol. Samples were then embedded in
poly(methyl methacrylate) and allowed to polymerize for 7 days. Sections were
cut from the center of each defect (bucco-lingually) with an Exakt band saw.
Polished ground sections (<100μm) were stained with
Sanderson’s rapid bone stain to qualitatively assess cellular
infiltration and bone regeneration.
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3

Bovine Tail-Derived IVD Culture

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IVDs were harvested from young (n ¼ 24, 6e8 months old) bovine tails obtained from the local abattoir, excised with a band saw (Exakt Apparatebau), rinsed in phosphate buffered saline (PBS) containing 10% penicillin-streptomycin 19 and cultured in:
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4

Micro Push-Out Testing of Dental Posts

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After the microscopic analysis a 1 mm thick slice was cut off from each labeled and microscopically analyzed sample using a band saw (Exakt Apparatebau) under constant water cooling and micro push-out testing was performed (Universal testing machine Zwick; Roell, Ulm, Germany) at a cross-head speed of 0.5 mm/min. With regard to the tapered design of the post, three different sizes of punch pins, as well as three different openings, were used for the push-out testing [18] (link).
The maximum stress was calculated from the recorded peak load divided by the computed surface. In order to calculate the exact bonding surface, the tapered design of the posts with regard to the respective part of the post was considered. Therefore, each specimen was measured using a micrometerscrew (MitutoyoMessgeräte,Neuss,Germany) and analyzed using a stereomicroscope (DV 4; Zeiss, Jena, Germany) to determine the cross-section dimension. The bonding surface was calculated using the formula of a conical frustrum and bond strengths was evaluated accordingly as previously described [18] (link)–[20] (link). The roots of the unlabeled specimens were sectioned perpendicular to the long axis of the root into six slices (thickness 1 mm) and the push-out tests were performed as above described.
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5

Femoral Specimen Preparation for Mechanical Analysis

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Macromechanical specimens were prepared from mid-diaphyseal sections of approximately 120 mm length that were cut approximately 100 mm below the cusp of the lesser trochanter (Figure 1). Each of the femoral sections was divided into two approximately 50 mm long pieces by a central cut perpendicular to the shaft using a band saw under constant water irrigation (Exakt Apparatebau, Norderstedt, Germany). The proximal piece was divided and three neighbouring specimens from the anterior-lateral region with a tetragonal cross-section of approximately 16 mm 2
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6

Histological Evaluation of Goat Intervertebral Disc Degeneration

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After obtaining MR images, all lumbar IVDs (T13L1–L5L6), including endplates were dissected from the spine and a 4 mm paramidsagittal slice was obtained using a band saw (Exakt, Norderstedt, Germany). Sections were fixed in 4% formaldehyde, decalcified in Kristensen's fluid, cut into 3 μm thin sections using a microtome, and stained with hematoxylin and eosin and Alcian Blue-Periodic Acid Schiff. Sections were analyzed using light microscopy, and degeneration grading was scored by two blinded independent researchers on different parameters optimized for goat IVD degeneration, as described and validated previously.33 (link) Differences in scoring between the observers were resolved by consensus, resulting in a final histological score ranging between 0 (healthy) and 6 (severely degenerated disc).
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7

Histological Evaluation of Bone Regeneration

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After fixation in formalin, the explanted mandibles were dehydrated in a graded series of ethanol and embedded in poly(methyl methacrylate). Using an Exakt band saw, sections were cut from each block in the center of the defect (bucco-lingually) using the µCT images as reference. The sections were then ground and polished to <100 µm using an Exakt grinding system, and stained with Sanderson’s rapid bone stain. New bone stained red, residual CM black, and infiltrating cells blue.
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8

Quantitative Morphometric Analysis of Stented Arteries

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For quantitative morphometric analysis, stented arterial segments were fixed overnight in 4 % formaldehyde after excision and stored in 70 % ethanol. The segments were dehydrated in a graded series of acetone and embedded in resin (methyl methacrylate and butyl methacrylate, 1:1). Sections (7 μm) were cut with a rotary microtome (Leica) from the middle of the stent, after sawing the segment with a band saw (Exakt). Sections were attached to glass slides and dried overnight.
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