microscope coverslips and slides (24 × 40) Search Results


90
Corning Life Sciences glass coverslip
Glass Coverslip, supplied by Corning Life Sciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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90
Avantor microscope cover slide
Microscope Cover Slide, supplied by Avantor, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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86
Fisher Scientific glass slides
Glass Slides, supplied by Fisher Scientific, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 86 stars, based on 1 article reviews
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99
Olympus slide scanning system
Slide Scanning System, supplied by Olympus, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Carl Roth GmbH microscopy slides × size
Microscopy Slides × Size, supplied by Carl Roth GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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90
Avantor 30 × 24 mm, #1.5, 0.16–0.19 mm thick borosilicate cover slips
30 × 24 Mm, #1.5, 0.16–0.19 Mm Thick Borosilicate Cover Slips, supplied by Avantor, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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90
Carl Roth GmbH coverslips
Coverslips, supplied by Carl Roth GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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93
Valiant Co Ltd glass microscope slide
Microscopy and single-virus detection of fusion events. (a) Flow cell attached to <t>microscope</t> holder with 2 mm tubing inserted in the channel hole for buffer exchange. Inset below shows a schematic of a single channel of the flow cell with labels. (b) Image of a microscope with flow cell setup during image acquisition. (c) Typical image before and 30 s after fusion is triggered by buffer exchange. Note that more Texas Red-labeled viral particles are visible after 30 s, as expected from dilutional dequenching upon fusion. Each individual red dot signifies a TR-labeled influenza viral particle, as illustrated by the cartoon on the right. (d) Fluorescence intensity is plotted versus time for a single viral particle with a dequenching spike apparent upon lipid mixing. The interval from buffer exchange (time = 0) to the dequenching spike (black vertical dashed line) is recorded as the single-event waiting time. (e) Waiting times for all individual fusion events are compiled into a cumulative distribution function. The shape of this distribution contains information about the underlying kinetic process and can be analyzed using gamma functions or randomness-parameter calculations.
Glass Microscope Slide, supplied by Valiant Co Ltd, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/microscope+coverslips+and+slides+(24+%C3%97+40)/7X+Cleaning+Solution/pmc11775682-55-5-32
Average 93 stars, based on 1 article reviews
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97
Carl Zeiss axio vert a1 microscope
Microscopy and single-virus detection of fusion events. (a) Flow cell attached to <t>microscope</t> holder with 2 mm tubing inserted in the channel hole for buffer exchange. Inset below shows a schematic of a single channel of the flow cell with labels. (b) Image of a microscope with flow cell setup during image acquisition. (c) Typical image before and 30 s after fusion is triggered by buffer exchange. Note that more Texas Red-labeled viral particles are visible after 30 s, as expected from dilutional dequenching upon fusion. Each individual red dot signifies a TR-labeled influenza viral particle, as illustrated by the cartoon on the right. (d) Fluorescence intensity is plotted versus time for a single viral particle with a dequenching spike apparent upon lipid mixing. The interval from buffer exchange (time = 0) to the dequenching spike (black vertical dashed line) is recorded as the single-event waiting time. (e) Waiting times for all individual fusion events are compiled into a cumulative distribution function. The shape of this distribution contains information about the underlying kinetic process and can be analyzed using gamma functions or randomness-parameter calculations.
Axio Vert A1 Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 97 stars, based on 1 article reviews
axio vert a1 microscope - by Bioz Stars, 2026-09
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90
Carl Roth GmbH microscope slides 1.5 h
Microscopy and single-virus detection of fusion events. (a) Flow cell attached to <t>microscope</t> holder with 2 mm tubing inserted in the channel hole for buffer exchange. Inset below shows a schematic of a single channel of the flow cell with labels. (b) Image of a microscope with flow cell setup during image acquisition. (c) Typical image before and 30 s after fusion is triggered by buffer exchange. Note that more Texas Red-labeled viral particles are visible after 30 s, as expected from dilutional dequenching upon fusion. Each individual red dot signifies a TR-labeled influenza viral particle, as illustrated by the cartoon on the right. (d) Fluorescence intensity is plotted versus time for a single viral particle with a dequenching spike apparent upon lipid mixing. The interval from buffer exchange (time = 0) to the dequenching spike (black vertical dashed line) is recorded as the single-event waiting time. (e) Waiting times for all individual fusion events are compiled into a cumulative distribution function. The shape of this distribution contains information about the underlying kinetic process and can be analyzed using gamma functions or randomness-parameter calculations.
Microscope Slides 1.5 H, supplied by Carl Roth GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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90
Harrick Plasma Inc plasma cleaning oven pcd-001
Microscopy and single-virus detection of fusion events. (a) Flow cell attached to <t>microscope</t> holder with 2 mm tubing inserted in the channel hole for buffer exchange. Inset below shows a schematic of a single channel of the flow cell with labels. (b) Image of a microscope with flow cell setup during image acquisition. (c) Typical image before and 30 s after fusion is triggered by buffer exchange. Note that more Texas Red-labeled viral particles are visible after 30 s, as expected from dilutional dequenching upon fusion. Each individual red dot signifies a TR-labeled influenza viral particle, as illustrated by the cartoon on the right. (d) Fluorescence intensity is plotted versus time for a single viral particle with a dequenching spike apparent upon lipid mixing. The interval from buffer exchange (time = 0) to the dequenching spike (black vertical dashed line) is recorded as the single-event waiting time. (e) Waiting times for all individual fusion events are compiled into a cumulative distribution function. The shape of this distribution contains information about the underlying kinetic process and can be analyzed using gamma functions or randomness-parameter calculations.
Plasma Cleaning Oven Pcd 001, supplied by Harrick Plasma Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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96
Nikon eclipse 200 optical microscope
Microscopy and single-virus detection of fusion events. (a) Flow cell attached to <t>microscope</t> holder with 2 mm tubing inserted in the channel hole for buffer exchange. Inset below shows a schematic of a single channel of the flow cell with labels. (b) Image of a microscope with flow cell setup during image acquisition. (c) Typical image before and 30 s after fusion is triggered by buffer exchange. Note that more Texas Red-labeled viral particles are visible after 30 s, as expected from dilutional dequenching upon fusion. Each individual red dot signifies a TR-labeled influenza viral particle, as illustrated by the cartoon on the right. (d) Fluorescence intensity is plotted versus time for a single viral particle with a dequenching spike apparent upon lipid mixing. The interval from buffer exchange (time = 0) to the dequenching spike (black vertical dashed line) is recorded as the single-event waiting time. (e) Waiting times for all individual fusion events are compiled into a cumulative distribution function. The shape of this distribution contains information about the underlying kinetic process and can be analyzed using gamma functions or randomness-parameter calculations.
Eclipse 200 Optical Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/microscope+coverslips+and+slides+(24+%C3%97+40)/MM-200/pmc05329856-131-19-18
Average 96 stars, based on 1 article reviews
eclipse 200 optical microscope - by Bioz Stars, 2026-09
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Image Search Results


Microscopy and single-virus detection of fusion events. (a) Flow cell attached to microscope holder with 2 mm tubing inserted in the channel hole for buffer exchange. Inset below shows a schematic of a single channel of the flow cell with labels. (b) Image of a microscope with flow cell setup during image acquisition. (c) Typical image before and 30 s after fusion is triggered by buffer exchange. Note that more Texas Red-labeled viral particles are visible after 30 s, as expected from dilutional dequenching upon fusion. Each individual red dot signifies a TR-labeled influenza viral particle, as illustrated by the cartoon on the right. (d) Fluorescence intensity is plotted versus time for a single viral particle with a dequenching spike apparent upon lipid mixing. The interval from buffer exchange (time = 0) to the dequenching spike (black vertical dashed line) is recorded as the single-event waiting time. (e) Waiting times for all individual fusion events are compiled into a cumulative distribution function. The shape of this distribution contains information about the underlying kinetic process and can be analyzed using gamma functions or randomness-parameter calculations.

Journal: JACS Au

Article Title: Single-Virus Microscopy of Biochemical Events in Viral Entry

doi: 10.1021/jacsau.4c00992

Figure Lengend Snippet: Microscopy and single-virus detection of fusion events. (a) Flow cell attached to microscope holder with 2 mm tubing inserted in the channel hole for buffer exchange. Inset below shows a schematic of a single channel of the flow cell with labels. (b) Image of a microscope with flow cell setup during image acquisition. (c) Typical image before and 30 s after fusion is triggered by buffer exchange. Note that more Texas Red-labeled viral particles are visible after 30 s, as expected from dilutional dequenching upon fusion. Each individual red dot signifies a TR-labeled influenza viral particle, as illustrated by the cartoon on the right. (d) Fluorescence intensity is plotted versus time for a single viral particle with a dequenching spike apparent upon lipid mixing. The interval from buffer exchange (time = 0) to the dequenching spike (black vertical dashed line) is recorded as the single-event waiting time. (e) Waiting times for all individual fusion events are compiled into a cumulative distribution function. The shape of this distribution contains information about the underlying kinetic process and can be analyzed using gamma functions or randomness-parameter calculations.

Article Snippet: Kapton polyimide tape (Ted Pella) Glass microscope slide (25 × 75 mm, 1.0 mm thickness) Polydimethylsiloxane SYLGARD 184 Silicone Elastomer Kit Glass coverslips (24 × 40 mm, #1.5 thickness) 7X cleaning solution (MP Biomedicals) PLL–PEG (SuSoS) PLL–PEG-Biotin (SuSoS) Reaction buffer (10 mM Sodium Phosphate Monobasic, 90 mM Sodium Citrate and 150 mM Sodium Chloride, pH 7.4 or 5.0 as indicated) Neutravidin (Fisher Scientific) Palmitoyl oleoylphosphatidylcholine (Avanti) Dioleoylphosphatidylethanolamine (Avanti) Cholesterol (Sigma) GD1a (Sigma) DHPE-Biotin (Avanti) DiYO-1 (AAT Bioquest) Virus of interest (X-31 H3N2 influenza is used as an example here) Texas Red-DHPE (Fisher Scientific) HEPES buffer (20 mM HEPES, 150 mM NaCl, buffered to pH 7.2) PD SpinTrap G-25 (Cytiva) Ceramic coverslip rack Scalpel 2 mm biopsy hole punch 2 mm tubing 1 mL Luer-lock syringe

Techniques: Microscopy, Virus, Buffer Exchange, Labeling, Fluorescence