For closed-environment format, microfluidic devices were first infused with PBS and pressurized to remove air bubbles inside the microwells using a manually operated syringe with outlet closed. The devices were filled with 1% BSA in PBS, and incubated at room temperature for 30 min to prevent attachment of cells and molecules on PDMS surfaces. Devices were then washed with PBS prior to cell and bead loading. To establish gravity-driven flow, device outlet was connected to a 10′ tubing with a one way stopcock connected at the end while the device inlet is left unconnected to serve as a reservoir. In this configuration, solutions were simply pipetted onto the inlet reservoir and withdrawn into the device through gravity-driven flow by adjusting the height difference between the inlet and the end of the tubing connected to outlet. The one way stopcock further allowed start/stop control over the fluid flow to facilitate cell and bead loading. Similarly, the flow could also be reversed by creating a higher hydrostatic pressure on the outlet side by adjusting the height of the tubing. During scRNA-seq experiments, a single cell suspension, 5000–10 000 cells in 50 μl PBS + 1%BSA solution, was pipetted on the inlet and withdrawn into the device. Once the channel was completely filled with cell solution, the fluid flow was stopped and cells were allowed to settle by gravity. Excess cells were washed out by PBS, and mRNA capture beads, 30 000–120 000 beads in 50–150 μl, were loaded similar to cells. Size exclusion and back-and-forth loading ensured loading of >99% of the microwells with a single bead. Excess beads were washed out with PBS, and 100–200 μl freeze-thaw lysis buffer was introduced into the devices. Fluorinated oil (Fluorinert FC-40), 100–200 μl in volume, was then withdrawn into the devices to seal the microwells. After oil sealing, the tubing at the outlet was disconnected, and the microfluidic devices were exposed to three freeze thaw cycles, 5 min freezing at –80°C freezer or dry ice/ethanol bath and 5 min thawing at room temperature. Following lysis, microfluidic device was incubated for an hour inside a wet chamber for mRNA capture onto beads. mRNA binding occurs in the freeze-thaw lysis buffer without the need for buffer exchange. After incubation, the inlet of the microfluidic device was connected to a syringe filled with 6× saline-sodium citrate (SSC) buffer and the outlet was connected to eppendorf tube with a tubing. The microfluidic device was then inverted and the beads were flushed out of the device into the tube by purging. Centrifugation of the microfluidic device in inverted orientation before purging or gentle tapping on the back of the microfluidic device with a tweezer during purging was used to help move the beads out of the microwells. We were able to recover >95% of the beads using this fashion. Collected beads were centrifuged at 1000g for 1 min, and washed twice with 6× SSC buffer prior to reverse transcription.
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Fluorinert
Fluorinert
Fluorinert: A Comprehensive Overview for Researchers
Fluorinert, a class of highly fluorinated, inert liquids, has emerged as a versatile tool in various scientific and industrial applications.
These chemically stable compounds offer unique properties, such as high thermal stability, low surface tension, and excellent electrical insulating characteristics, making them ideal for diverse research endeavors.
This MeSH term description provides researchers with a concise yet informative overview of Fluorinert, highlighting its key features and potential applications.
Discover how this remarkable family of compounds can enhance your research, from thermal management to electrical insulation and beyond.
Explore the latest advancements and unlock the full potential of Fluorinert in your field of study.
Whether you're working with Fluorinert for the first time or seeking to optimize your existing protocols, this description will serve as a valuable resource, guiding you towards the future of Fluorinert research.
Fluorinert, a class of highly fluorinated, inert liquids, has emerged as a versatile tool in various scientific and industrial applications.
These chemically stable compounds offer unique properties, such as high thermal stability, low surface tension, and excellent electrical insulating characteristics, making them ideal for diverse research endeavors.
This MeSH term description provides researchers with a concise yet informative overview of Fluorinert, highlighting its key features and potential applications.
Discover how this remarkable family of compounds can enhance your research, from thermal management to electrical insulation and beyond.
Explore the latest advancements and unlock the full potential of Fluorinert in your field of study.
Whether you're working with Fluorinert for the first time or seeking to optimize your existing protocols, this description will serve as a valuable resource, guiding you towards the future of Fluorinert research.
Most cited protocols related to «Fluorinert»
Bath
Buffers
Cell-Matrix Junction
Cells
Centrifugation
Dry Ice
Ethanol
Fluorinert
Freezing
Gravity
Hydrostatic Pressure
Medical Devices
Microchip Analytical Devices
Reverse Transcription
RNA, Messenger
Saline Solution
Single-Cell RNA-Seq
Sodium Citrate
Syringes
The fixed samples were transferred to the Basque Center on Cognition, Brain and Language (BCBL, Donostia - San Sebastian, Spain) for MRI scanning. Ex vivo MR images of the whole brains were acquired on a 3 T Magnetom TIM Trio scanner with a 12 channel receiver coil. Despite its reduced efficiency compared with the 32 channel counterpart, the 12 channel coil enables acquisition at higher resolution without running out of RAM in the image reconstruction. The brains were scanned in vacuum bags filled with Fluorinert FC-3283 (3M, Maplewood, MN, U.S.A.), in order to minimize the negative impact of air bubbles and susceptibility artifacts. The images were acquired with a 3D multi-slab balanced steady-state free precession sequence (McNab et al., 2009 (link)) with TE/TR = 5.3/10.6 ms and flip angle . Four axial slabs with 112 slices each were used to cover the whole volume of the brains, and 57% slice oversampling was used in order to minimize slab aliasing. The resolution of the scans was 0.25 mm isotropic, with matrix size 720 720 448 voxels (axial). MR images were acquired with four different RF phase increments (0, 90, 180, 270°) and averaged to reduce banding artifacts. The time of acquisition per phase was 90 min. Ten repetitions of this protocol were acquired for increased signal-to-noise ratio (SNR). The total length of the protocol was thus 60 h.
Combined with the 12 channel receiver coil, the multi-slab acquisition described above enabled us to bypass the memory limitations of our clinical scanner when reconstructing the images, while preserving the SNR efficiency of 3D acquisitions. However, this type of acquisition also introduces slab boundary artifacts at the interfaces between the slabs. After computing a brain mask with simple Otsu thresholding (Otsu, 1975 ), such artifacts were corrected simultaneously with the bias field using a Bayesian method (Iglesias et al., 2016 ). Sample slices of the MRI scans are shown inFig. 1 .Fig. 1 ![]()
Combined with the 12 channel receiver coil, the multi-slab acquisition described above enabled us to bypass the memory limitations of our clinical scanner when reconstructing the images, while preserving the SNR efficiency of 3D acquisitions. However, this type of acquisition also introduces slab boundary artifacts at the interfaces between the slabs. After computing a brain mask with simple Otsu thresholding (Otsu, 1975 ), such artifacts were corrected simultaneously with the bias field using a Bayesian method (Iglesias et al., 2016 ). Sample slices of the MRI scans are shown in
(a) Sample sagittal slice of ex vivo MRI scan of case NHL8_14. (b) Corrected for bias field and slab boundary artifacts. (c) Close-up of left thalami in coronal view, uncorrected. (d) Corrected version of (c).
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Brain
Cognition
Fluorinert
HAVCR2 protein, human
Memory
MRI Scans
Radionuclide Imaging
Susceptibility, Disease
Thalamus
TRIO protein, human
Vacuum
Autopsy
Brain
Cranium
ECHO protocol
Fluorinert
fluorocarbon 77
Gadolinium
Gray Matter
Mice, Inbred C57BL
Protons
Radionuclide Imaging
Susceptibility, Disease
Wounds
To help reduce any stress, all drugs were infused in the home cages. The stylets in the guide cannulae were replaced by a double infusion cannula (33 gauge, Plastics One) connected to two 5 μl microsyringes (WPI) in a microinfusion pump (Native Instruments) via flexible plastic tubing (C232CS, Plastics One) filled with Fluorinert (3M). The tips of infusion cannulae projected 0.5 mm below the tip of the guide cannulae. For intra-hippocampal microinjection, 0.5 μl of drug per cannula was infused at 0.2 μl min−1 (2.5 min). Infusion cannulas were left in place for a further 2.5 min before being replaced with stylets to aid drug absorption. For intra-VTA microinjection, 0.3 μl was injected at a rate of 0.3 μl min−1 (1 min) followed by 1-min of waiting. The mice were habituated to the experimental procedure of injection and to vehicle injection prior to the drug test in order to minimize novelty effect. Mice received drug injection 20 min (hippocampal microinfusions and i.p. injection of clonidine) or 3 min (VTA microinfusions) prior to the novelty exploration.
Cannula
Clonidine
Fluorinert
Microinjections
Mus
Pharmaceutical Preparations
Substance Abuse Detection
Dietary Fiber
ECHO protocol
Fluorinert
fluorocarbon 77
Gills
Pulse Rate
Pulses
Radionuclide Imaging
Spectroscopy, Nuclear Magnetic Resonance
Spectrum Analysis
Submersion
Susceptibility, Disease
Tissues
Most recents protocols related to «Fluorinert»
Mycobacterium bovis (BCG, Tokyo strain) was purchased from Japan BCG Laboratory (Tokyo, Japan) and maintained in BD BACTEC™ MGIT™ medium supplemented with OADC Enrichment and PANTA antibiotic mixture (Becton Dickinson Co., 245122, Franklin Lakes, NJ) at 37 °C. Mid-log-phase BCG was prepared at concentrations of 1000 CFU/µl for time-lapse microscopy and 10,000 CFU/µl for drug susceptibility testing in MGIT media by using a bacterium counting chamber (A161, SANSYO, Tokyo, Japan). RFP, INH, PZA, SM, EB, LVFX, TH, and CS were obtained from FUJIFILM Wako (Tokyo, Japan). KM and EVM were obtained from Nacalai Tesque (Tokyo, Japan) and Asahi-Kasei Pharma (Tokyo, Japan), respectively. DLM and BDQ were obtained from Selleck (Houston, TX). These chemicals were dissolved in deionized water (INH, PZA, SM, EB, TH, KM, EVM, and CS), methanol (RFP, TH), 0.1 N hydrochloride (LVFX), or dimethyl sulfoxide (DLM, BDQ), and then sterilized using 0.22-µm MILLEX-GV syringe filters (Millipore, Burlington, MA) prior to being added to MGIT media under aseptic conditions. Perfluorocarbon (Fluorinert™, FC-3283) was obtained from 3M (Maplewood, MN). Live/Dead™ BacLight™ bacterial viability reagent was purchased from Thermo Fisher Scientific (L13152, Waltham, MA). Detailed information on the antibacterial agents used in this study is shown in Supplementary Table 1 .
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Anti-Bacterial Agents
Antibiotics
Asepsis
Bacterial Viability
Fluorinert
Fluorocarbons
Methanol
Microscopy
Mycobacterium bovis
Strains
Sulfoxide, Dimethyl
Susceptibility, Disease
Syringes
Dissected spinal cords were placed in a glass tube filled with fluorinert FC-770A (3M™ Electronic Liquids, Saint Paul, MI, USA) within a solenoid antenna. The coil was specifically designed for spinal cord studies [37 (link)]. Acquisitions were performed with a 9.4 Tesla MRI (Agilent Varian 9.4/160/ASR, Santa Clara, CA, USA) associated with a VnmrJ acquisition system (Agilent, Palo Alto, CA, USA). Acquisition parameters were the following: spin-echo multi slice (SEMS, TR = 1580 ms TE = 30.55 ms, NE = 1, AVG = 30, FOV = 10 × 10, 36 slides, thickness = 1 mm, gap = 0 mm, acquisition matrix (NREAD*NPHASE = 128 × 128). Diffusion gradients were applied in three directions (Gs = 10 G/cm; delta = 6.844 ms; separation = 15.05 ms; b-value = 499.21 s/mm2). Regions of interest were manually segmented using Myrian software (Intrasens, Montpellier, France) and data were processed using a MATLAB-based in-house toolbox, as we previously described [34 (link)]. The following parameters were analyzed: lesion area at the epicenter, lesion extension, and lesion volume. Number of C57BL6/6J mice included in the MRI study: 18 C57BL6/6J experimental mice (12 females and 6 males); 19 control mice (12 females and 7 males). Animals were sacrificed at 6 weeks after SCI.
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Animals
Diffusion
ECHO protocol
Females
Fluorinert
Males
Mice, House
Spinal Cord
All protocols were approved by the Loma Linda University Animal Health and Safety Committee and are in compliance with federal regulations (protocol #813033, approved 09/17/2013). All experiments were conducted following the ARRIVE guidelines. Male adult Sprague Dawley rats (329.8 ± 3.3 g, Harlan; n = 24) recovered in the vivarium for 5–7 days prior to transcardiac perfusion using 4% paraformaldehyde (PFA, Electron Microscopy Sciences, Hatfield, PA, USA). Though imaging of either the brain in the cranial vault [30 (link)] or of the brain alone has been reported, brain-only samples have been used to generate atlases [31 (link)]. Therefore, we elected to remove the brains from the cranial vault. Brains were postfixed in 4% PFA, washed and stored at 4 °C in 0.1M PBS/0.05% sodium azide until imaging and histology. Together, these procedures reduced the potential for artifacts particularly at high field strengths. Prior to imaging, brains were placed in Fluorinert (FC-770, SynQuest Labs, Inc., Alachua, FL, USA) to facilitate susceptibility matched imaging.
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Adult
Animals
Brain
Calvaria
Electron Microscopy
Fluorinert
Loma
Males
paraform
Perfusion
Rats, Sprague-Dawley
Safety
Sodium Azide
Susceptibility, Disease
Top-gate/bottom-contact SWCNT network
transistors were fabricated on cleaned glass slides (sodium-free aluminum
borosilicate glass, Schott AF32 eco, 20 × 25 mm2,
thickness 0.3 mm). The interdigitated bottom electrodes (channel length L = 10 and 20 μm with channel width W = 10 mm or L = 40 μm with W = 5 mm) were patterned by photolithography using a double-layer
photoresist (LOR5B (MicroChem)/ MICROPOSIT S1813 (Dow Chemical)).
An adhesion layer of 2 nm of chromium and 30 nm of gold was deposited
by electron beam evaporation, followed by lift-off in N-methyl-2-pyrrolidone (NMP, Sigma-Aldrich, 99%) and a cleaning step
with ultrasonication in acetone and 2-propanol. Prior to deposition
of (6,5) SWCNTs, the substrates were treated in a UV/ozone cleaner
for 10 min, rinsed with 2-propanol, blow-dried with nitrogen, and
annealed for 5 min at 100 °C. To obtain homogeneous networks,
the (6,5) SWCNTs were spin-coated onto the substrates three times
(30 s, 2000 rpm). After each spin-coating step, the substrates were
heated for 2 min at 90 °C. To remove excess polymer, the samples
were washed with tetrahydrofuran (VWR International, analytical grade)
and 2-propanol and subsequently heated for 4 min at 90 °C. The
linear density of the resulting SWCNT networks was 30 nanotubes/μm
with an average SWCNT length of 1.2 ± 0.4 μm, as determined
by atomic force microscopy (AFM, Bruker Dimension Icon). SWCNTs outside
the channel area were removed by oxygen plasma etching while SWCNTs
within the channel were protected with photolithographically patterned
photoresist as described above. After the subsequent lift-off in NMP
and annealing for 45 min at 300 °C in dry nitrogen, selected
samples were doped by submerging the substrates in a 3 or 6 g·L–1 solution of 1,2,4,5-tetrakis(tetramethylguanidino)benzene
(ttmgb)52 (link) in anhydrous toluene for 20 min,
followed by annealing for 20 min at 150 °C. Polymeric dielectric
films with thicknesses of about 50 nm were deposited in a dry nitrogen
atmosphere by spin-coating and successive annealing: Teflon AF2400
(poly[4,5-difluoro-2,2-bis(trifluoromethyl)-1,3-dioxole-co-tetrafluoroethylene], Sigma-Aldrich, 53 nm from 20 g·L–1 solution in FluorInert FC-40 (3M)); P(VDF-TrFE-CTFE)
(poly(vinylidene fluoride-co-trifluoroethylene-co-chlorotrifluoroethylene) Piezotech RT TS, Piezotech Arkema,
52 nm from 10 g·L–1 in n-butanone); PMMA (poly(methyl
methacrylate), PolymerSource, MW = 315
kg·mol–1, syndiotactic, 50 nm from 20 g·L–1 in n-butyl acetate); PS (polystyrene, Mw = 230.4 kg·mol–1, atactic,
50 nm from 20 g·L–1 in n-butyl
acetate). 60 nm of HfOx were deposited
via atomic layer deposition (ALD, Ultratech Savannah S100) at 100
°C with tetrakis(dimethylamino)hafnium (Strem Chemicals Inc.)
and water as precursors either as the top layer of a hybrid dielectric
or as a single dielectric layer directly on the SWCNTs. Thermal evaporation
of 30 nm thick silver gate electrodes through a shadow mask completed
the devices. Due to the conformal encapsulation with ALD-HfOx, all devices were air-stable.
transistors were fabricated on cleaned glass slides (sodium-free aluminum
borosilicate glass, Schott AF32 eco, 20 × 25 mm2,
thickness 0.3 mm). The interdigitated bottom electrodes (channel length L = 10 and 20 μm with channel width W = 10 mm or L = 40 μm with W = 5 mm) were patterned by photolithography using a double-layer
photoresist (LOR5B (MicroChem)/ MICROPOSIT S1813 (Dow Chemical)).
An adhesion layer of 2 nm of chromium and 30 nm of gold was deposited
by electron beam evaporation, followed by lift-off in N-methyl-2-pyrrolidone (NMP, Sigma-Aldrich, 99%) and a cleaning step
with ultrasonication in acetone and 2-propanol. Prior to deposition
of (6,5) SWCNTs, the substrates were treated in a UV/ozone cleaner
for 10 min, rinsed with 2-propanol, blow-dried with nitrogen, and
annealed for 5 min at 100 °C. To obtain homogeneous networks,
the (6,5) SWCNTs were spin-coated onto the substrates three times
(30 s, 2000 rpm). After each spin-coating step, the substrates were
heated for 2 min at 90 °C. To remove excess polymer, the samples
were washed with tetrahydrofuran (VWR International, analytical grade)
and 2-propanol and subsequently heated for 4 min at 90 °C. The
linear density of the resulting SWCNT networks was 30 nanotubes/μm
with an average SWCNT length of 1.2 ± 0.4 μm, as determined
by atomic force microscopy (AFM, Bruker Dimension Icon). SWCNTs outside
the channel area were removed by oxygen plasma etching while SWCNTs
within the channel were protected with photolithographically patterned
photoresist as described above. After the subsequent lift-off in NMP
and annealing for 45 min at 300 °C in dry nitrogen, selected
samples were doped by submerging the substrates in a 3 or 6 g·L–1 solution of 1,2,4,5-tetrakis(tetramethylguanidino)benzene
(ttmgb)52 (link) in anhydrous toluene for 20 min,
followed by annealing for 20 min at 150 °C. Polymeric dielectric
films with thicknesses of about 50 nm were deposited in a dry nitrogen
atmosphere by spin-coating and successive annealing: Teflon AF2400
(poly[4,5-difluoro-2,2-bis(trifluoromethyl)-1,3-dioxole-co-tetrafluoroethylene], Sigma-Aldrich, 53 nm from 20 g·L–1 solution in FluorInert FC-40 (3M)); P(VDF-TrFE-CTFE)
(poly(vinylidene fluoride-co-trifluoroethylene-co-chlorotrifluoroethylene) Piezotech RT TS, Piezotech Arkema,
52 nm from 10 g·L–1 in n-butanone); PMMA (poly(methyl
methacrylate), PolymerSource, MW = 315
kg·mol–1, syndiotactic, 50 nm from 20 g·L–1 in n-butyl acetate); PS (polystyrene, Mw = 230.4 kg·mol–1, atactic,
50 nm from 20 g·L–1 in n-butyl
acetate). 60 nm of HfOx were deposited
via atomic layer deposition (ALD, Ultratech Savannah S100) at 100
°C with tetrakis(dimethylamino)hafnium (Strem Chemicals Inc.)
and water as precursors either as the top layer of a hybrid dielectric
or as a single dielectric layer directly on the SWCNTs. Thermal evaporation
of 30 nm thick silver gate electrodes through a shadow mask completed
the devices. Due to the conformal encapsulation with ALD-HfOx, all devices were air-stable.
1-Propanol
Acetone
Ataxia
Benzene
butyl acetate
chlorotrifluoroethylene
Chromium
Cocaine
Electrons
Fluorinert
Gold
Hafnium
Hybrids
Isopropyl Alcohol
Medical Devices
methylethyl ketone
Methylmethacrylate
Microscopy, Atomic Force
Nitrogen
Oxygen
Ozone
Plasma
Poly A
Polymers
Polymethyl Methacrylate
Polystyrenes
polyvinylidene fluoride
S100 Proteins
Silver
Sodium
Suby's G solution
Teflon
tetrafluoroethylene
tetrahydrofuran
Toluene
trifluoroethene
To remove background field effects and to keep the brain moist, formalin- fixed brains were placed in a plastic container filled with 3M fluorinert electronic liquid (FC-770, Parallax Technology, Inc.), which had the similar susceptibility as the brain40 (link). The brains were rocked gently in room temperature for 12–24 h to allow air bubbles to escape40 (link)–42 (link). MRI scans were acquired at a 3T Siemens Trio MRI scanner with a 32-channel head coil (Siemens Medical Solutions) using 3D multi-echo gradient recalled echo (GRE) and 3D T2-weighted turbo spin echo sequences. For the initial 5 brains, multi-echo GRE scans were acquired in 112 slices of 0.5 mm thickness (no gap), with field of view = 224 mm2, matrix size = 448 × 448, repetition time = 50 ms, echo time (TE)1/spacing/TE9 = 5/5/45 ms, flip angle = 20°, number of excitations = 4. The initial 5 T2 scans were acquired in 224 slices of 0.5 mm thickness (no gap), with field of view = 256 mm2, matrix size = 512 × 512, repetition time = 3,200 ms, TE = 371 ms, Turbo factor = 269, number of excitations = 2. To minimize susceptibility artifacts caused by residual water/air bubbles, the subsequent 12 multi-echo GRE scans were acquired in 240 slices of 0.6 mm thickness (no gap), with field of view = 224 mm2, matrix size = 384 × 384, repetition time = 30 ms, TE1/spacing/TE6 = 2.25/2.25/13.50 ms, flip angle = 20°, number of excitations = 4. The subsequent 12 T2 scans were acquired in 288 slices of 0.5 mm thickness (no gap), with field of view = 256 mm2, matrix size = 512 × 512, repetition time = 3,200 ms, TE = 371 ms, Turbo factor = 269, number of excitations = 3.
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Brain
ECHO protocol
Fluorinert
Formalin
Head
MRI Scans
Radionuclide Imaging
Susceptibility, Disease
TRIO protein, human
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Fluorinert is a line of inert, thermally stable, and chemically resistant liquids developed by 3M. These liquids are primarily used as coolants, heat-transfer fluids, and dielectric media in various laboratory and industrial applications. Fluorinert products are designed to provide efficient thermal management while maintaining chemical inertness and non-flammability.
Sourced in United States
Fluorinert FC-40 is a clear, colorless, and odorless liquid manufactured by Merck Group. It is a perfluorinated compound that exhibits high chemical and thermal stability, as well as low surface tension and low viscosity. Fluorinert FC-40 is commonly used as a heat transfer fluid and dielectric medium in various industrial and laboratory applications.
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The BPX-30 is a versatile laboratory equipment designed for a variety of analytical applications. It features a precise temperature control system and a durable construction to ensure reliable performance. The core function of the BPX-30 is to facilitate sample preparation and analysis tasks in a laboratory environment.
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Sourced in Sao Tome and Principe
FC-72 Fluorinert is a clear, colorless, and odorless liquid that is commonly used as a coolant and heat transfer medium in various laboratory applications. It has a high thermal and chemical stability, a low viscosity, and a low surface tension, making it suitable for applications where efficient heat transfer and low reactivity are required.
Sourced in United States
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The Achieva 3.0T TX is a magnetic resonance imaging (MRI) system produced by Philips. It is a 3.0 Tesla (T) superconducting magnet-based MRI scanner designed for high-performance imaging.
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Fluorinert FC-40 is a clear, colorless, and odorless liquid manufactured by 3M. It is an inert, fluorinated liquid with a high boiling point and low surface tension. Fluorinert FC-40 is primarily used as an electronic coolant and in other industrial applications where a thermally and chemically stable liquid is required.
Sourced in Sao Tome and Principe
Fluorinert FC-770 is a clear, colorless, and odorless fluorinated liquid produced by 3M. It has a boiling point of 97°C and is non-flammable. The product is designed for use as a heat transfer fluid in laboratory and industrial applications.
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FC-770 is a high-performance fluorinated solvent developed by 3M. It is a clear, colorless liquid with a low surface tension and high density. FC-770 is primarily used as a cleaning and degreasing agent in industrial and laboratory settings.
More about "Fluorinert"
Fluorinated Inert Liquids: Unlocking the Versatility of Fluorinert for Cutting-Edge Research Fluorinert, a remarkable class of highly fluorinated, chemically stable liquids, has emerged as a game-changer in the world of scientific and industrial research.
These unique compounds, also known as perfluorinated liquids or perfluorocarbons, offer a tantalizing array of properties that make them indispensable tools for researchers across diverse fields.
Harnessing the Power of Fluorinert: From Thermal Management to Electrical Insulation Fluorinert's exceptional thermal stability, low surface tension, and excellent dielectric characteristics make it a prime choice for applications ranging from thermal management and cooling systems to electrical insulation and high-voltage equipment.
Researchers in fields like electronics, cryogenics, and aerospace engineering have embraced Fluorinert's versatility, leveraging its remarkable capabilities to push the boundaries of innovation.
Exploring the Fluorinert Family: Variations and Specialized Applications Within the Fluorinert family, researchers have access to a diverse range of specialized compounds, each with its own unique set of properties and applications.
Fluorinert FC-40, BPX-30, FC-72, Fluorinert (FC-770), and Achieva 3.0T TX are just a few examples of the Fluorinert variants that have captivated the scientific community.
Each of these compounds offers distinct advantages, allowing researchers to tailor their experimental setups and protocols to their specific needs.
Navigating the Fluorinert Landscape: Optimizing Your Research Protocols As the field of Fluorinert research continues to evolve, researchers are constantly seeking ways to enhance their workflows and unlock new discoveries.
The AI-driven platform at PubCompare.ai can be a valuable ally in this endeavor, empowering researchers to locate the best protocols from literature, preprints, and patents, and optimize their Fluorinert-based experiments for maximum reproducibility and accuracy.
Embrace the Future of Fluorinert Research: Explore, Innovate, and Achieve Whether you're a seasoned Fluorinert researcher or just embarking on your journey, this comprehensive overview serves as a stepping stone to unlocking the full potential of these remarkable compounds.
Dive into the world of Fluorinert, explore its diverse applications, and witness the transformative impact it can have on your research.
The future of scientific discovery is here, and Fluorinert is leading the way.
These unique compounds, also known as perfluorinated liquids or perfluorocarbons, offer a tantalizing array of properties that make them indispensable tools for researchers across diverse fields.
Harnessing the Power of Fluorinert: From Thermal Management to Electrical Insulation Fluorinert's exceptional thermal stability, low surface tension, and excellent dielectric characteristics make it a prime choice for applications ranging from thermal management and cooling systems to electrical insulation and high-voltage equipment.
Researchers in fields like electronics, cryogenics, and aerospace engineering have embraced Fluorinert's versatility, leveraging its remarkable capabilities to push the boundaries of innovation.
Exploring the Fluorinert Family: Variations and Specialized Applications Within the Fluorinert family, researchers have access to a diverse range of specialized compounds, each with its own unique set of properties and applications.
Fluorinert FC-40, BPX-30, FC-72, Fluorinert (FC-770), and Achieva 3.0T TX are just a few examples of the Fluorinert variants that have captivated the scientific community.
Each of these compounds offers distinct advantages, allowing researchers to tailor their experimental setups and protocols to their specific needs.
Navigating the Fluorinert Landscape: Optimizing Your Research Protocols As the field of Fluorinert research continues to evolve, researchers are constantly seeking ways to enhance their workflows and unlock new discoveries.
The AI-driven platform at PubCompare.ai can be a valuable ally in this endeavor, empowering researchers to locate the best protocols from literature, preprints, and patents, and optimize their Fluorinert-based experiments for maximum reproducibility and accuracy.
Embrace the Future of Fluorinert Research: Explore, Innovate, and Achieve Whether you're a seasoned Fluorinert researcher or just embarking on your journey, this comprehensive overview serves as a stepping stone to unlocking the full potential of these remarkable compounds.
Dive into the world of Fluorinert, explore its diverse applications, and witness the transformative impact it can have on your research.
The future of scientific discovery is here, and Fluorinert is leading the way.