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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, 2026-10
90/100 stars

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Related Articles

Microarray:

Article Title: Synergetic improvements of sensitivity and specificity of nanowire field effect transistor gene chip by designing neutralized DNA as probe
Article Snippet: .. To immobilize the probes on the chip surface, 10 mM sodium phosphate buffer containing 1 μM probe DNA (regular, fully neutralized, or partially neutralized chimeric DNA) was prepared to spot on the NW by using a microarray spotter (SmartArrayer 136, CapitalBio Corporation, China) and incubated with the FET chip overnight. ..


Article Title: Allele-selective lowering of mutant HTT protein by HTT-LC3 linker compounds.
Article Snippet: .. Each compound was dissolved in DMSO at a concentration of 10 mM and printed in duplicates along vertical direction on homemade phenyl-isocyanate functionalized glass slides with a contact microarray printer (SmartArrayer 136, CapitalBio Corporation). ..

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: Developing an Efficient and General Strategy for Immobilization of Small Molecules onto Microarrays Using Isocyanate Chemistry
Article Snippet: .. Five biotinylated compounds, biotin-(PEG) 2 -NH 2 , biotin4-nitrophenyl ester, biotin-NH-NH 2 , biotin-(PEG) 6 -OH, and D-biotin (with intrinsic COOH group), were printed on as-prepared isocyanate functionalized glass slides with a contact microarray printer (SmartArrayer 136 Microarray Spotter, CapitalBio Corporation, Beijing, China). ..

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). ..

Incubation:

Article Title: Synergetic improvements of sensitivity and specificity of nanowire field effect transistor gene chip by designing neutralized DNA as probe
Article Snippet: .. To immobilize the probes on the chip surface, 10 mM sodium phosphate buffer containing 1 μM probe DNA (regular, fully neutralized, or partially neutralized chimeric DNA) was prepared to spot on the NW by using a microarray spotter (SmartArrayer 136, CapitalBio Corporation, China) and incubated with the FET chip overnight. ..

Concentration Assay:


Article Title: Allele-selective lowering of mutant HTT protein by HTT-LC3 linker compounds.
Article Snippet: .. Each compound was dissolved in DMSO at a concentration of 10 mM and printed in duplicates along vertical direction on homemade phenyl-isocyanate functionalized glass slides with a contact microarray printer (SmartArrayer 136, CapitalBio Corporation). ..

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). ..

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. ..

other:

Article Title: Bioinformatics and microarray analysis of microRNA expression profiles of murine embryonic stem cells, neural stem cells induced from ESCs and isolated from E8·5 mouse neural tube
Article Snippet: To better understand whether microRNAs (miRNAs) are involved in the self-renewal of stem cells and fate determination of neural stem cells and to identify the miRNA expression patterns of different neural stem cells (NSC) in vitro and in vivo, we examined miRNA expression profiles of murine embryonic stem cells (ESC), NSC induced from ESC and isolated from E8.5 mouse neural tube (E8.5-NSC) using microarray technique.. It was found that a total of 40 miRNAs had similar expression level in all the three cells [false discovery rate (FDR)50, fold change ,3.0].. Moreover, q-PCR showed that some members of miR-106b and miR-17–92 families were expressed in the ESC, NSC induced from ESC (ESC-NSC) and hematopoietic stem cells (HSC).



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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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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.
Contact Microarray Printer, supplied by BioDot 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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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