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CapitalBio Corporation contact microarray printer smartarrayer 136
Contact Microarray Printer Smartarrayer 136, supplied by CapitalBio Corporation, 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/contact+microarray+printer/contact+microarray+printer+smartarrayer+136/pm40249703-755-24-29
Average 90 stars, based on 1 article reviews
contact microarray printer smartarrayer 136 - by Bioz Stars, 2026-11
90/100 stars

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Concentration Assay:


Article Title: Pharmacological boosting of cGAS activation sensitizes chemotherapy by enhancing antitumor immunity.
Article Snippet: .. Each compound was dissolved in DMSO to a concentration of 10 mM and printed in duplicate on home-made phenyl-isocyanate functionalized slide with a contact microarray printer (SmartArrayer 136, CapitalBio Corporation, Beijing, China).89 Biotin-BSA at a concentration of 7 600 nM in 13 phosphate-buffered saline (PBS) and biotin-(PEG)2-NH2 at a concentration of 5 mM in DMSOwere also printed as the inner and the outer borders of SMMs to serve as positionmarkers and positive controls. ..

Article Title: P53 upregulation by USP7-engaging molecular glues.
Article Snippet: .. Each compound was dissolved in dimethyl sulfoxide (DMSO) at a concentration of 10 mmol/L and printed in duplicate along a vertical direction on homemade phenyl-isocyanate functionalized glass slides with a contact microarray printer (SmartArrayer 136; CapitalBio Corporation, Beijing, China). ..

Microarray:


Article Title: Pharmacological boosting of cGAS activation sensitizes chemotherapy by enhancing antitumor immunity.
Article Snippet: .. Each compound was dissolved in DMSO to a concentration of 10 mM and printed in duplicate on home-made phenyl-isocyanate functionalized slide with a contact microarray printer (SmartArrayer 136, CapitalBio Corporation, Beijing, China).89 Biotin-BSA at a concentration of 7 600 nM in 13 phosphate-buffered saline (PBS) and biotin-(PEG)2-NH2 at a concentration of 5 mM in DMSOwere also printed as the inner and the outer borders of SMMs to serve as positionmarkers and positive controls. ..

Article Title: P53 upregulation by USP7-engaging molecular glues.
Article Snippet: .. Each compound was dissolved in dimethyl sulfoxide (DMSO) at a concentration of 10 mmol/L and printed in duplicate along a vertical direction on homemade phenyl-isocyanate functionalized glass slides with a contact microarray printer (SmartArrayer 136; CapitalBio Corporation, Beijing, China). ..

Article Title: Systematic Identification of Protein Targets of Sub5 Using Saccharomyces cerevisiae Proteome Microarrays
Article Snippet: Briefly, using Liquidator 96 manual pipetting system (Mettler Toledo Rainin, LLC, Oakland, CA, USA), Saccharomyces cerevisiae purified proteins in 96-well plates were transferred to 384-well plates. .. High throughput CapitalBio SmartArrayerTM 136 microarrays contact printer (Capitalbio Corporation, Beijing, China) with 48 microarray pins were used for spotting (in duplicate) the entire ~5800 individual Saccharomyces cerevisiae proteins, and several landmark proteins on the aldehyde-coated glass slides to fabricate Saccharomyces cerevisiae proteome microarrays. ..

Article Title: Multiplexed Analysis of Photochemical Oxidants Using a Nanoparticle-Based Optoelectronic Nose.
Article Snippet: Photochemical pollutants pose a substantial threat to human health in both outdoor and indoor environments.. Herein, we prepare a class of gold nanoparticle-based colorimetric sensor arrays on optimized hydrophobic substrates using a simple pin-printing method for accurate identification and quantification of various gas-phase oxidants, as these microdetectors are low cost, sensitive, and easy to fabricate.. For an array of AuNP sensors modified with various thiol-terminated ligands, a unique and distinguishable change in color (i.e., red, green, and blue response patterns) was obtained for each specific pollutant for molecular fingerprinting.

Article Title: Development and application of a novel triplex protein microarray method for rapid detection of antibodies against avian influenza virus, Newcastle disease virus, and avian infectious bronchitis virus.
Article Snippet: Avian influenza virus (AIV), Newcastle disease virus (NDV), and avian infectious bronchitis virus (IBV) inflict immense damage on the global poultry industry annually.. Serological diagnostic methods are fundamental for the effective control and prevention of outbreaks caused by these viruses.. In this study, a novel triplex protein microarray assay was developed and validated for the rapid and simultaneous visualized detection of antibodies against AIV, NDV, and IBV in chicken sera.

Article Title: R406 and its structural analogs reduce SNCA/α-synuclein levels via autophagic degradation.
Article Snippet: .. Each compound was printed twice in a vertical direction on homemade glass slides functionalized with phenyl-isocyanate using a contact microarray printer (SmartArrayer 136, CapitalBio Corporation, Beijing, China). ..

Saline:

Article Title: Pharmacological boosting of cGAS activation sensitizes chemotherapy by enhancing antitumor immunity.
Article Snippet: .. Each compound was dissolved in DMSO to a concentration of 10 mM and printed in duplicate on home-made phenyl-isocyanate functionalized slide with a contact microarray printer (SmartArrayer 136, CapitalBio Corporation, Beijing, China).89 Biotin-BSA at a concentration of 7 600 nM in 13 phosphate-buffered saline (PBS) and biotin-(PEG)2-NH2 at a concentration of 5 mM in DMSOwere also printed as the inner and the outer borders of SMMs to serve as positionmarkers and positive controls. ..

High Throughput Screening Assay:

Article Title: Systematic Identification of Protein Targets of Sub5 Using Saccharomyces cerevisiae Proteome Microarrays
Article Snippet: Briefly, using Liquidator 96 manual pipetting system (Mettler Toledo Rainin, LLC, Oakland, CA, USA), Saccharomyces cerevisiae purified proteins in 96-well plates were transferred to 384-well plates. .. High throughput CapitalBio SmartArrayerTM 136 microarrays contact printer (Capitalbio Corporation, Beijing, China) with 48 microarray pins were used for spotting (in duplicate) the entire ~5800 individual Saccharomyces cerevisiae proteins, and several landmark proteins on the aldehyde-coated glass slides to fabricate Saccharomyces cerevisiae proteome microarrays. ..

Glass:

Article Title: Multiplexed Analysis of Photochemical Oxidants Using a Nanoparticle-Based Optoelectronic Nose.
Article Snippet: Photochemical pollutants pose a substantial threat to human health in both outdoor and indoor environments.. Herein, we prepare a class of gold nanoparticle-based colorimetric sensor arrays on optimized hydrophobic substrates using a simple pin-printing method for accurate identification and quantification of various gas-phase oxidants, as these microdetectors are low cost, sensitive, and easy to fabricate.. For an array of AuNP sensors modified with various thiol-terminated ligands, a unique and distinguishable change in color (i.e., red, green, and blue response patterns) was obtained for each specific pollutant for molecular fingerprinting.



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The VANC-D4 assay (A) Fabrication of the VANC-D4 assay. SI-ATRP is used to grow POEGMA-co-GMA brushes on glass slides. Following SI-ATRP, VANC-BSA is <t>inkjet</t> printed into the polymer brush to create stable spots and fluorescently labeled anti-VANC antibodies (termed dAb) are printed on trehalose pads to create labile spots. (B) Sequential steps of the VANC-D4 assay. The steps of the VANC-D4 are (i) dispensing a blood sample on the surface, (ii) dissolution of the trehalose pads to release the fluorescently labeled dAb into solution, (iii) diffusion of the labeled dAb in the sample volume, (iv) detection of fluorescence signal from the antibody bound to immobilized VANC-BSA. (C) Representative VANC-D4 assay response in the presence of (i) no drug, (ii) low drug, and (iii) high drug concentration. (D) VANC monitoring across its clinical range using VANC-spiked whole blood diluted 100-fold in running buffer, analyzed in triplicate. The clinical range for the test is 1–45 μg/mL. Intensity values are shown, with error bars that represent the standard error of the means for n = 3 separate runs. The LOD for the presented dose-response curve was calculated to be 0.8 μg/mL.
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CapitalBio Corporation contact microarray printer smartarrayer 136
The VANC-D4 assay (A) Fabrication of the VANC-D4 assay. SI-ATRP is used to grow POEGMA-co-GMA brushes on glass slides. Following SI-ATRP, VANC-BSA is <t>inkjet</t> printed into the polymer brush to create stable spots and fluorescently labeled anti-VANC antibodies (termed dAb) are printed on trehalose pads to create labile spots. (B) Sequential steps of the VANC-D4 assay. The steps of the VANC-D4 are (i) dispensing a blood sample on the surface, (ii) dissolution of the trehalose pads to release the fluorescently labeled dAb into solution, (iii) diffusion of the labeled dAb in the sample volume, (iv) detection of fluorescence signal from the antibody bound to immobilized VANC-BSA. (C) Representative VANC-D4 assay response in the presence of (i) no drug, (ii) low drug, and (iii) high drug concentration. (D) VANC monitoring across its clinical range using VANC-spiked whole blood diluted 100-fold in running buffer, analyzed in triplicate. The clinical range for the test is 1–45 μg/mL. Intensity values are shown, with error bars that represent the standard error of the means for n = 3 separate runs. The LOD for the presented dose-response curve was calculated to be 0.8 μg/mL.
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The VANC-D4 assay (A) Fabrication of the VANC-D4 assay. SI-ATRP is used to grow POEGMA-co-GMA brushes on glass slides. Following SI-ATRP, VANC-BSA is <t>inkjet</t> printed into the polymer brush to create stable spots and fluorescently labeled anti-VANC antibodies (termed dAb) are printed on trehalose pads to create labile spots. (B) Sequential steps of the VANC-D4 assay. The steps of the VANC-D4 are (i) dispensing a blood sample on the surface, (ii) dissolution of the trehalose pads to release the fluorescently labeled dAb into solution, (iii) diffusion of the labeled dAb in the sample volume, (iv) detection of fluorescence signal from the antibody bound to immobilized VANC-BSA. (C) Representative VANC-D4 assay response in the presence of (i) no drug, (ii) low drug, and (iii) high drug concentration. (D) VANC monitoring across its clinical range using VANC-spiked whole blood diluted 100-fold in running buffer, analyzed in triplicate. The clinical range for the test is 1–45 μg/mL. Intensity values are shown, with error bars that represent the standard error of the means for n = 3 separate runs. The LOD for the presented dose-response curve was calculated to be 0.8 μg/mL.
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The VANC-D4 assay (A) Fabrication of the VANC-D4 assay. SI-ATRP is used to grow POEGMA-co-GMA brushes on glass slides. Following SI-ATRP, VANC-BSA is <t>inkjet</t> printed into the polymer brush to create stable spots and fluorescently labeled anti-VANC antibodies (termed dAb) are printed on trehalose pads to create labile spots. (B) Sequential steps of the VANC-D4 assay. The steps of the VANC-D4 are (i) dispensing a blood sample on the surface, (ii) dissolution of the trehalose pads to release the fluorescently labeled dAb into solution, (iii) diffusion of the labeled dAb in the sample volume, (iv) detection of fluorescence signal from the antibody bound to immobilized VANC-BSA. (C) Representative VANC-D4 assay response in the presence of (i) no drug, (ii) low drug, and (iii) high drug concentration. (D) VANC monitoring across its clinical range using VANC-spiked whole blood diluted 100-fold in running buffer, analyzed in triplicate. The clinical range for the test is 1–45 μg/mL. Intensity values are shown, with error bars that represent the standard error of the means for n = 3 separate runs. The LOD for the presented dose-response curve was calculated to be 0.8 μg/mL.
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Image Search Results


The VANC-D4 assay (A) Fabrication of the VANC-D4 assay. SI-ATRP is used to grow POEGMA-co-GMA brushes on glass slides. Following SI-ATRP, VANC-BSA is inkjet printed into the polymer brush to create stable spots and fluorescently labeled anti-VANC antibodies (termed dAb) are printed on trehalose pads to create labile spots. (B) Sequential steps of the VANC-D4 assay. The steps of the VANC-D4 are (i) dispensing a blood sample on the surface, (ii) dissolution of the trehalose pads to release the fluorescently labeled dAb into solution, (iii) diffusion of the labeled dAb in the sample volume, (iv) detection of fluorescence signal from the antibody bound to immobilized VANC-BSA. (C) Representative VANC-D4 assay response in the presence of (i) no drug, (ii) low drug, and (iii) high drug concentration. (D) VANC monitoring across its clinical range using VANC-spiked whole blood diluted 100-fold in running buffer, analyzed in triplicate. The clinical range for the test is 1–45 μg/mL. Intensity values are shown, with error bars that represent the standard error of the means for n = 3 separate runs. The LOD for the presented dose-response curve was calculated to be 0.8 μg/mL.

Journal: iScience

Article Title: A rapid point-of-care test for vancomycin monitoring at the clinical bedside

doi: 10.1016/j.isci.2026.116064

Figure Lengend Snippet: The VANC-D4 assay (A) Fabrication of the VANC-D4 assay. SI-ATRP is used to grow POEGMA-co-GMA brushes on glass slides. Following SI-ATRP, VANC-BSA is inkjet printed into the polymer brush to create stable spots and fluorescently labeled anti-VANC antibodies (termed dAb) are printed on trehalose pads to create labile spots. (B) Sequential steps of the VANC-D4 assay. The steps of the VANC-D4 are (i) dispensing a blood sample on the surface, (ii) dissolution of the trehalose pads to release the fluorescently labeled dAb into solution, (iii) diffusion of the labeled dAb in the sample volume, (iv) detection of fluorescence signal from the antibody bound to immobilized VANC-BSA. (C) Representative VANC-D4 assay response in the presence of (i) no drug, (ii) low drug, and (iii) high drug concentration. (D) VANC monitoring across its clinical range using VANC-spiked whole blood diluted 100-fold in running buffer, analyzed in triplicate. The clinical range for the test is 1–45 μg/mL. Intensity values are shown, with error bars that represent the standard error of the means for n = 3 separate runs. The LOD for the presented dose-response curve was calculated to be 0.8 μg/mL.

Article Snippet: Following polymerization, D4 assays were fabricated using non-contact inkjet printing methods as described elsewhere., VANC-BSA was printed using a non-contact inkjet microarray printer (Scienion, sciFLEXARRAYER Type S12).

Techniques: Polymer, Labeling, Dissolution, Diffusion-based Assay, Fluorescence, Concentration Assay