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Full Moon BioSystems cy3 full moon biosystems scanner calibration slide
Functionalization of a glass substrate to increase cell retention. (A) Epoxy coating of a glass substrate followed by streptavidin conjugation and binding of biotinylated cells. (B) Fluorescent imagining of <t>SA-Cy3</t> coating on epoxy slides and negative control/unmodified slides. Streptavidin density determined using the Cy3 <t>calibration</t> slide (scale bar = 1 mm).
Cy3 Full Moon Biosystems Scanner Calibration Slide, supplied by Full Moon BioSystems, 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/result/cy3 full moon biosystems scanner calibration slide/product/Full Moon BioSystems
Average 90 stars, based on 1 article reviews
cy3 full moon biosystems scanner calibration slide - by Bioz Stars, 2026-03
90/100 stars

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1) Product Images from "Increased Retention of Cardiac Cells to a Glass Substrate through Streptavidin–Biotin Affinity"

Article Title: Increased Retention of Cardiac Cells to a Glass Substrate through Streptavidin–Biotin Affinity

Journal: ACS Omega

doi: 10.1021/acsomega.1c02003

Functionalization of a glass substrate to increase cell retention. (A) Epoxy coating of a glass substrate followed by streptavidin conjugation and binding of biotinylated cells. (B) Fluorescent imagining of SA-Cy3 coating on epoxy slides and negative control/unmodified slides. Streptavidin density determined using the Cy3 calibration slide (scale bar = 1 mm).
Figure Legend Snippet: Functionalization of a glass substrate to increase cell retention. (A) Epoxy coating of a glass substrate followed by streptavidin conjugation and binding of biotinylated cells. (B) Fluorescent imagining of SA-Cy3 coating on epoxy slides and negative control/unmodified slides. Streptavidin density determined using the Cy3 calibration slide (scale bar = 1 mm).

Techniques Used: Conjugation Assay, Binding Assay, Negative Control



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Functionalization of a glass substrate to increase cell retention. (A) Epoxy coating of a glass substrate followed by streptavidin conjugation and binding of biotinylated cells. (B) Fluorescent imagining of <t>SA-Cy3</t> coating on epoxy slides and negative control/unmodified slides. Streptavidin density determined using the Cy3 <t>calibration</t> slide (scale bar = 1 mm).
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Functionalization of a glass substrate to increase cell retention. (A) Epoxy coating of a glass substrate followed by streptavidin conjugation and binding of biotinylated cells. (B) Fluorescent imagining of <t>SA-Cy3</t> coating on epoxy slides and negative control/unmodified slides. Streptavidin density determined using the Cy3 <t>calibration</t> slide (scale bar = 1 mm).
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Functionalization of a glass substrate to increase cell retention. (A) Epoxy coating of a glass substrate followed by streptavidin conjugation and binding of biotinylated cells. (B) Fluorescent imagining of <t>SA-Cy3</t> coating on epoxy slides and negative control/unmodified slides. Streptavidin density determined using the Cy3 <t>calibration</t> slide (scale bar = 1 mm).
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Functionalization of a glass substrate to increase cell retention. (A) Epoxy coating of a glass substrate followed by streptavidin conjugation and binding of biotinylated cells. (B) Fluorescent imagining of <t>SA-Cy3</t> coating on epoxy slides and negative control/unmodified slides. Streptavidin density determined using the Cy3 <t>calibration</t> slide (scale bar = 1 mm).
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Functionalization of a glass substrate to increase cell retention. (A) Epoxy coating of a glass substrate followed by streptavidin conjugation and binding of biotinylated cells. (B) Fluorescent imagining of <t>SA-Cy3</t> coating on epoxy slides and negative control/unmodified slides. Streptavidin density determined using the Cy3 <t>calibration</t> slide (scale bar = 1 mm).
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Functionalization of a glass substrate to increase cell retention. (A) Epoxy coating of a glass substrate followed by streptavidin conjugation and binding of biotinylated cells. (B) Fluorescent imagining of <t>SA-Cy3</t> coating on epoxy slides and negative control/unmodified slides. Streptavidin density determined using the Cy3 <t>calibration</t> slide (scale bar = 1 mm).
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Functionalization of a glass substrate to increase cell retention. (A) Epoxy coating of a glass substrate followed by streptavidin conjugation and binding of biotinylated cells. (B) Fluorescent imagining of SA-Cy3 coating on epoxy slides and negative control/unmodified slides. Streptavidin density determined using the Cy3 calibration slide (scale bar = 1 mm).

Journal: ACS Omega

Article Title: Increased Retention of Cardiac Cells to a Glass Substrate through Streptavidin–Biotin Affinity

doi: 10.1021/acsomega.1c02003

Figure Lengend Snippet: Functionalization of a glass substrate to increase cell retention. (A) Epoxy coating of a glass substrate followed by streptavidin conjugation and binding of biotinylated cells. (B) Fluorescent imagining of SA-Cy3 coating on epoxy slides and negative control/unmodified slides. Streptavidin density determined using the Cy3 calibration slide (scale bar = 1 mm).

Article Snippet: Using a Cy3 Full Moon Biosystems scanner calibration slide, the fluorescent signal obtained from an Affymetrix 428 Array scanner could be directly related to the fluorophore density on the glass surface.

Techniques: Conjugation Assay, Binding Assay, Negative Control