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Vannas spring scissors

Manufactured by Fine Science Tools
Sourced in United States

Vannas spring scissors are a type of laboratory scissor designed for precise cutting of delicate materials. They feature a spring-loaded mechanism that helps to reduce hand fatigue during extended use. The scissors have sharp, fine-tipped blades made of high-quality stainless steel.

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15 protocols using vannas spring scissors

1

Induction of Experimental Periodontitis in Mice

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To induce experimental periodontitis, wild-type C57BL/6j mice (6- to 8-week-old) were used. The animals were anesthetized by intraperitoneal injection of a cocktail of ketamine (80 mg/kg) and xylazine (10 mg/kg). This cocktail allows us to anesthetize animals for at least 30 min. After mice were anaesthetized, a silk ligature (5-0 silk threads, Johnson & Johnson, New Brunswick, NJ, USA) was placed on the upper left second molar and left for 24 h, 3, and 7 days as described (Abe and Hajishengallis, 2013 (link)). Briefly, a ligature was placed through the proximal contacts of the upper left second molar until reached the gingival margin. The procedure was performed using two Castroviejo micro needle holder (Fine Science Tools, CA, USA) under the stereomicroscope assistance (Seiler Evolution xR6, Seiler Microscope, MO, USA). Suture was tied firmly with a double-knot on the buccal side. Altogether, 10–15 min was required for successful ligature placement. The excess suture was cut using Vannas spring scissors (Fine Science Tools, CA, USA). The upper right second molar without ligature was used as a control.
This study was conducted in strict accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health and the experimental procedures were approved by the Forsyth Institutional Animal Care and Use Committee (IACUC).
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2

Interopercular-mandibular Ligament Transection

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Interopercular-mandibular (IOM) ligament transection surgery was adapted from Smeeton et al.18 (link). Briefly, adult zebrafish were anesthetized with Tricaine MS-222 and restrained in a damp sponge. Using 3-mm Vannas spring scissors (Fine Science Tools, cat. #1500000), the IOM ligament was severed with a single cut and a pull test performed on the IOP bone to confirm transection. Fish were then revived in clean system water, housed on-system, and received daily post-operative health checks for three days. At experimental endpoints, zebrafish were euthanized using a lethal dose of Tricaine MS-222 with rapid chilling on ice.
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3

Dissection and Isolation of Lumbosacral DRGs

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Dissections were performed under a Nikon SMZ645 stereo microscope. Mice were euthanized by carbon dioxide inhalation followed by cervical dislocation. Mice were laid on the dorsal side and immobilized on a dissection pad. Skin covering the ventral thorax and abdomen was removed together with internal organs to fully expose the ventral spinal column using surgical scissors (Fine Science Tools, #14054-13), supported by tissue forceps (Fine Science Tools, #11021-12). Muscles covering ventral side of the spinal column were removed using Spring Scissors (Fine Science Tools, #15751-11) to expose the lumbosacral peripheral nerves. To expose the lumbosacral DRGs, the ventral vertebrae were removed using the aforementioned Spring Scissors, aided by Octagon forceps (Fine Science Tools, #11042-08) with care taken not to sever nerves. DRGs were gently picked starting with the lower lumbar level (L6) using a Dumont #3 forceps (World Precision Instruments, #50037) and isolated by cutting connecting nerves with Vannas Spring Scissors (Fine Science Tools, #15000-00).
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4

Antennal Removal and Sleep Analysis

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All three antennal segments of 1- to 2-day-old flies were physically removed using 3 mm Vannas Spring Scissors (Fine Science Tools, Foster City, CA). After 3 days of recovery, flies were loaded into monitor tubes for sleep analysis.
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5

Dissection and TMRM Staining of Drosophila Larva

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Late third instar wandering larvae are dissected in freshly prepared Schneider’s medium (pH 7.4, S9895, Sigma) with 5 mM EGTA. Larval dissection is as previously described [77 ] in a chamber glass slide coated with a thin layer of Sylgard (Dow Corning Corporation, MI). The larva is opened along the dorsal midline with Vannas spring scissors (15000-00, Fine Science Tools), then the body wall muscles are pinned on the slide and the main guts and salivary glands are carefully removed. The larva is then washed gently three times using fresh Schneider’s medium with 5 mM EGTA, and kept in the same medium for imaging. For TMRM staining, 20 nM TMRM (Molecular Probes) is added to Schneider’s medium with 5 mM EGTA and mixed evenly, and then applied to the dissected larva for 20 min in the dark. After TMRM staining, the larva is washed three times again with fresh Schneider’s medium with 5 mM EGTA and kept in the same medium with 5 nM TMRM for imaging.
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6

Zebrafish IOM Ligament Transection

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IOM ligament transection was performed on 8–12 months post-fertilization adult zebrafish using 3-mm Vannas spring scissors (Fine Science Tools, cat. #1500000). The fish were anesthetized using MS222 and placed ventral side up on a wet sponge, and a single cut was performed to transect the ligament. Transection was confirmed by manual pulling of the IOP bone.
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7

Single-cell RNA-seq of Embryoid Bodies

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CO were collected for single cell capture (N=3) at 100 days after initial seeding of embryoid body. CO were dissociated using papain solution containing DNase (Worthington). CO were washed 3 times using PBS, and then cut up using Vannas Spring Scissors (Fine Science Tools). Samples were then incubated in 2 mL papain solution at 37°C for 1 hr, and samples were triturated by manually pipetting every 20 mins during the 1 hr incubation period. Dissociated cells were then filtered through a 40 μm cell strainer, and centrifuged at 300G for 5 mins, papain removed and resuspended in 1% FBS in PBS. Using the Chromium Single Cell 3’ Reagent Kits v3.1 (10X Genomics), 4000–7000 cells were captured per lane, single-cell libraries were sequenced on a NovaSeq S2 flow cell.
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8

Antennal Removal and Sleep Analysis

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All three antennal segments of 1- to 2-day-old flies were physically removed using 3 mm Vannas Spring Scissors (Fine Science Tools, Foster City, CA). After 3 days of recovery, flies were loaded into monitor tubes for sleep analysis.
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9

Spinal Cord Lesioning in Mice

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Mice were deeply anaesthetized with isoflurane, spinal level C5 (or C3) was exposed by laminectomy and the dorsal columns were lesioned at a depth of 1mm with Vannas spring scissors (Fine Science Tools, Foster City, CA). The dorsal musculature was sutured with 4-0 silk sutures and the skin was closed with wound clips. Mice were randomly selected for C3 lesion or C3 sham (laminectomy only) groups.
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10

Surgical Exposure of Dorsal Root Ganglia

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Mice were anesthetized with ketamine (100 mg/kg BW) and xylazine (10 mg/kg BW) and received a subcutaneous injection of buprenorphine (0.05 mg/kg BW). The skin and muscles were separated exposing unilaterally the region of 11th, 12th and 13th thoracic vertebrae and the dorsal region transverse processes. To expose the DRGs, transverse processes were trimmed with a micro drill (Roboz Surgical Instrument). Whole DRGs were carefully cut with tipped Dumont #5 forceps and Vannas spring scissors (Fine Science Tools) without disrupting the spinal cord. Dorsal muscle layer was then closed with interrupted suture technique with Polyamide Monofilament (B. Braun). The overlying skin was sutured using 9 mm autoclips (Braintree Scientific).
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