slide glass 76×26 Search Results


glass slides 26 x 76 x  (Avantor)
90
Avantor glass slides 26 x 76 x
Glass Slides 26 X 76 X, 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
https://www.bioz.com/product/slide+glass+76%C3%9726/glass+slides+26+x+76+x/pm37565596-299-1-9
Average 90 stars, based on 1 article reviews
glass slides 26 x 76 x - by Bioz Stars, 2026-10
90/100 stars
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glass microscopy slides 76 × 26  (Corning Life Sciences)
90
Corning Life Sciences glass microscopy slides 76 × 26
Experimental setup of high-throughput droplet-based cytotoxicity platform. ( A ) Experimental schematics showing cytotoxicity platform that combines (i) droplet generation and cell pairing using microfluidics, (ii) droplet immobilization for real-time <t>microscopy,</t> (iii) automated image analysis using custom-made MATLAB script to allow unbiased and high throughput detection of cytotoxic events. Stained NK cells and K562 cells were loaded into the chip using 200 µL pipette tips and encapsulated into droplets using a 3-inlet microfluidic chip. The viability dyes were included within the cell medium. The immobilized droplets were incubated in a stage top incubator set at 5% CO 2 and 37 °C. Image acquisition was performed at every hour interval for 10 h. ( B ) The three-inlet microfluidic device with flow-focusing junction to generate droplets. ( C ) A qualitative test of the observation chamber was performed by monitoring droplets movement in the chamber under the microscope for 10 h.
Glass Microscopy Slides 76 × 26, 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
https://www.bioz.com/product/slide+glass+76%C3%9726/glass+microscopy+slides+76+%C3%97+26/pmc08385055-51-0-9
Average 90 stars, based on 1 article reviews
glass microscopy slides 76 × 26 - by Bioz Stars, 2026-10
90/100 stars
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microscope slides iso 8037/i  (Carl Roth GmbH)
90
Carl Roth GmbH microscope slides iso 8037/i
Experimental setup of high-throughput droplet-based cytotoxicity platform. ( A ) Experimental schematics showing cytotoxicity platform that combines (i) droplet generation and cell pairing using microfluidics, (ii) droplet immobilization for real-time <t>microscopy,</t> (iii) automated image analysis using custom-made MATLAB script to allow unbiased and high throughput detection of cytotoxic events. Stained NK cells and K562 cells were loaded into the chip using 200 µL pipette tips and encapsulated into droplets using a 3-inlet microfluidic chip. The viability dyes were included within the cell medium. The immobilized droplets were incubated in a stage top incubator set at 5% CO 2 and 37 °C. Image acquisition was performed at every hour interval for 10 h. ( B ) The three-inlet microfluidic device with flow-focusing junction to generate droplets. ( C ) A qualitative test of the observation chamber was performed by monitoring droplets movement in the chamber under the microscope for 10 h.
Microscope Slides Iso 8037/I, 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
https://www.bioz.com/product/slide+glass+76%C3%9726/glass+surfaces++microscope+slides+iso+8037+i++76+9+26+9+/pmc02842725-64-11-19
Average 90 stars, based on 1 article reviews
microscope slides iso 8037/i - by Bioz Stars, 2026-10
90/100 stars
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standard microscope glass slides corners cut, without frosted edge, 26 × 76  (Carl Roth GmbH)
90
Carl Roth GmbH standard microscope glass slides corners cut, without frosted edge, 26 × 76
Experimental setup of high-throughput droplet-based cytotoxicity platform. ( A ) Experimental schematics showing cytotoxicity platform that combines (i) droplet generation and cell pairing using microfluidics, (ii) droplet immobilization for real-time <t>microscopy,</t> (iii) automated image analysis using custom-made MATLAB script to allow unbiased and high throughput detection of cytotoxic events. Stained NK cells and K562 cells were loaded into the chip using 200 µL pipette tips and encapsulated into droplets using a 3-inlet microfluidic chip. The viability dyes were included within the cell medium. The immobilized droplets were incubated in a stage top incubator set at 5% CO 2 and 37 °C. Image acquisition was performed at every hour interval for 10 h. ( B ) The three-inlet microfluidic device with flow-focusing junction to generate droplets. ( C ) A qualitative test of the observation chamber was performed by monitoring droplets movement in the chamber under the microscope for 10 h.
Standard Microscope Glass Slides Corners Cut, Without Frosted Edge, 26 × 76, 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
https://www.bioz.com/product/slide+glass+76%C3%9726/standard+microscope+glass+slides+corners+cut++without+frosted+edge++26+%C3%97+76/pm38872416-42-0-6
Average 90 stars, based on 1 article reviews
standard microscope glass slides corners cut, without frosted edge, 26 × 76 - by Bioz Stars, 2026-10
90/100 stars
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a non-fluorescent commercial 76×26×1 mm3 glass slide in accordance with iso 8037/1  (Waldemar Knittel Glasbearbeitungs)
90
Waldemar Knittel Glasbearbeitungs a non-fluorescent commercial 76×26×1 mm3 glass slide in accordance with iso 8037/1
Experimental setup of high-throughput droplet-based cytotoxicity platform. ( A ) Experimental schematics showing cytotoxicity platform that combines (i) droplet generation and cell pairing using microfluidics, (ii) droplet immobilization for real-time <t>microscopy,</t> (iii) automated image analysis using custom-made MATLAB script to allow unbiased and high throughput detection of cytotoxic events. Stained NK cells and K562 cells were loaded into the chip using 200 µL pipette tips and encapsulated into droplets using a 3-inlet microfluidic chip. The viability dyes were included within the cell medium. The immobilized droplets were incubated in a stage top incubator set at 5% CO 2 and 37 °C. Image acquisition was performed at every hour interval for 10 h. ( B ) The three-inlet microfluidic device with flow-focusing junction to generate droplets. ( C ) A qualitative test of the observation chamber was performed by monitoring droplets movement in the chamber under the microscope for 10 h.
A Non Fluorescent Commercial 76×26×1 Mm3 Glass Slide In Accordance With Iso 8037/1, supplied by Waldemar Knittel Glasbearbeitungs, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/slide+glass+76%C3%9726/a+non+fluorescent+commercial+76%C3%9726%C3%971+mm3+glass+slide+in+accordance+with+iso+8037+1/10__1016_slash_j__surfcoat__2006__02__082-44-10-12
Average 90 stars, based on 1 article reviews
a non-fluorescent commercial 76×26×1 mm3 glass slide in accordance with iso 8037/1 - by Bioz Stars, 2026-10
90/100 stars
  Buy from Supplier
glass slides 76 × 26  (SCHOTT)
90
SCHOTT glass slides 76 × 26
Experimental setup of high-throughput droplet-based cytotoxicity platform. ( A ) Experimental schematics showing cytotoxicity platform that combines (i) droplet generation and cell pairing using microfluidics, (ii) droplet immobilization for real-time <t>microscopy,</t> (iii) automated image analysis using custom-made MATLAB script to allow unbiased and high throughput detection of cytotoxic events. Stained NK cells and K562 cells were loaded into the chip using 200 µL pipette tips and encapsulated into droplets using a 3-inlet microfluidic chip. The viability dyes were included within the cell medium. The immobilized droplets were incubated in a stage top incubator set at 5% CO 2 and 37 °C. Image acquisition was performed at every hour interval for 10 h. ( B ) The three-inlet microfluidic device with flow-focusing junction to generate droplets. ( C ) A qualitative test of the observation chamber was performed by monitoring droplets movement in the chamber under the microscope for 10 h.
Glass Slides 76 × 26, supplied by SCHOTT, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/slide+glass+76%C3%9726/glass+slides+76+%C3%97+26/pm38258390-181-1-16
Average 90 stars, based on 1 article reviews
glass slides 76 × 26 - by Bioz Stars, 2026-10
90/100 stars
  Buy from Supplier

Image Search Results


Experimental setup of high-throughput droplet-based cytotoxicity platform. ( A ) Experimental schematics showing cytotoxicity platform that combines (i) droplet generation and cell pairing using microfluidics, (ii) droplet immobilization for real-time microscopy, (iii) automated image analysis using custom-made MATLAB script to allow unbiased and high throughput detection of cytotoxic events. Stained NK cells and K562 cells were loaded into the chip using 200 µL pipette tips and encapsulated into droplets using a 3-inlet microfluidic chip. The viability dyes were included within the cell medium. The immobilized droplets were incubated in a stage top incubator set at 5% CO 2 and 37 °C. Image acquisition was performed at every hour interval for 10 h. ( B ) The three-inlet microfluidic device with flow-focusing junction to generate droplets. ( C ) A qualitative test of the observation chamber was performed by monitoring droplets movement in the chamber under the microscope for 10 h.

Journal: Scientific Reports

Article Title: An automated real-time microfluidic platform to probe single NK cell heterogeneity and cytotoxicity on-chip

doi: 10.1038/s41598-021-96609-9

Figure Lengend Snippet: Experimental setup of high-throughput droplet-based cytotoxicity platform. ( A ) Experimental schematics showing cytotoxicity platform that combines (i) droplet generation and cell pairing using microfluidics, (ii) droplet immobilization for real-time microscopy, (iii) automated image analysis using custom-made MATLAB script to allow unbiased and high throughput detection of cytotoxic events. Stained NK cells and K562 cells were loaded into the chip using 200 µL pipette tips and encapsulated into droplets using a 3-inlet microfluidic chip. The viability dyes were included within the cell medium. The immobilized droplets were incubated in a stage top incubator set at 5% CO 2 and 37 °C. Image acquisition was performed at every hour interval for 10 h. ( B ) The three-inlet microfluidic device with flow-focusing junction to generate droplets. ( C ) A qualitative test of the observation chamber was performed by monitoring droplets movement in the chamber under the microscope for 10 h.

Article Snippet: Glass microscopy slides (76 × 26 × 1 mm; Corning) were used as top and bottom covers (76 × 26 × 1 mm).

Techniques: High Throughput Screening Assay, Microscopy, Staining, Transferring, Incubation