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CapitalBio Corporation personalarrayertm16 microarray spotter
Personalarrayertm16 Microarray Spotter, 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/microarray+spotter/personalarrayertm16+microarray+spotter/us09650665-960-24-27
Average 90 stars, based on 1 article reviews
personalarrayertm16 microarray spotter - by Bioz Stars, 2026-09
90/100 stars

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other:

Article Title: Nano-Diamond-Enhanced Integrated Response of a Surface Plasmon Resonance Biosensor.
Article Snippet: Nanoimprinting as performed using a hot-pressing machine (Personal Arrayer 16 Microarray Spotter, CapitalBio Corp., Beijing, China).

Article Title: Nano-Diamond-Enhanced Integrated Response of a Surface Plasmon Resonance Biosensor.
Article Snippet: Nanoimprinting was performed using a hot-pressing machine (Personal Arrayer 16 Microarray Spotter, CapitalBio Corp., Beijing, China).

DNA Array:

Article Title: Development and post-functionalization of a colorless universal coating using Bis(vinyl sulfonyl)methane
Article Snippet: Herein we reported a colorless universal and stable coating through Bis(vinyl sulfonyl)methane (BVS) polymerization that occurs on a broad range of inorganic and organic material surfaces.. A set of organic bases were screened, and 1-methylimidazole was selected as the initiator.. Michael addition, polymerization and crosslinking were proposed as the major stages for the coating growth.

Microarray:

Article Title: Development and post-functionalization of a colorless universal coating using Bis(vinyl sulfonyl)methane
Article Snippet: Herein we reported a colorless universal and stable coating through Bis(vinyl sulfonyl)methane (BVS) polymerization that occurs on a broad range of inorganic and organic material surfaces.. A set of organic bases were screened, and 1-methylimidazole was selected as the initiator.. Michael addition, polymerization and crosslinking were proposed as the major stages for the coating growth.

Article Title: Detection of target nucleic acid sequence on solid phase by PTO cleavage and extension using HCTO assay
Article Snippet: .. The IO and marker dissolved in NSB spotting buffer at the final concentration of 50 μM were printed on the NSB9 NHS slides with PersonalArrayerTM16 Microarray Spotter (CapitalBio, China). ..

Article Title: Preparation and characterization of DNA array slides via surface Michael addition.
Article Snippet: Preparation and characterization of DNA array slides via surface Michael addition Fang Cheng, Xiaochun Ma, Qiancheng Feng, Hanqi Wang, Meng Yin, and Wei He Citation: Biointerphases 14, 061003 (2019); doi: 10.1063/1.5124411 View online: https://doi.org/10.1063/1.5124411 View Table of Contents: https://avs.scitation.org/toc/bip/14/6 Published by the American Vacuum Society Preparation and characterization of DNA array slides via surface Michael addition Fang Cheng,1,2,a) Xiaochun Ma,1,2 Qiancheng Feng,1,2 Hanqi Wang,1,2 Meng Yin,1,2 and Wei He1,2 1State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian, Liaoning 116023, China 2School of Chemical Engineering, Dalian University of Technology, Dalian, Liaoning 116023, China (Received 14 August 2019; accepted 28 October 2019; published 21 November 2019) The reliability and stability of array slides are a big concern for array vendors and end users.. Herein, we report on a new type of array slide with high reactivity toward DNA probes and low side reaction.. A one-step surface reaction via the Michael addition involved in preparing array slides was developed and characterized by x-ray photoelectron spectroscopy, contact angle, and fluorescence labeling.

Article Title: Laboratory and clinical evaluation of a microarray for the detection of ATP7B mutations in Wilson disease in China
Article Snippet: .. Probes were then spotted on the surface of the aldehyde group–based microarray slide (CapitalBio) using a PersonalArrayerTM 16 spotting instrument (CapitalBio). ..

Microscopy:

Article Title: Identification EXOSC4 as a novel autoantigen of interstitial lung disease in rheumatoid arthritis.
Article Snippet: Keep the polymer 3D substrates (CapitalBio, Beijing, China) at 4 °C, take them out before use, and let them to return room temperature. .. The PersonalArrayerTM16 contact printing device (CapitalBio, Beijing, China) is used to attach pre-printing adhesion microscope slides (Citotest, Jiangsu, China) and polymer 3D substrates, with the program parameters configured for pre-printing 90 iterations, followed by repeating the printing process 3 times. ..

Polymer:

Article Title: Identification EXOSC4 as a novel autoantigen of interstitial lung disease in rheumatoid arthritis.
Article Snippet: Keep the polymer 3D substrates (CapitalBio, Beijing, China) at 4 °C, take them out before use, and let them to return room temperature. .. The PersonalArrayerTM16 contact printing device (CapitalBio, Beijing, China) is used to attach pre-printing adhesion microscope slides (Citotest, Jiangsu, China) and polymer 3D substrates, with the program parameters configured for pre-printing 90 iterations, followed by repeating the printing process 3 times. ..

Marker:

Article Title: Detection of target nucleic acid sequence on solid phase by PTO cleavage and extension using HCTO assay
Article Snippet: .. The IO and marker dissolved in NSB spotting buffer at the final concentration of 50 μM were printed on the NSB9 NHS slides with PersonalArrayerTM16 Microarray Spotter (CapitalBio, China). ..

Concentration Assay:

Article Title: Detection of target nucleic acid sequence on solid phase by PTO cleavage and extension using HCTO assay
Article Snippet: .. The IO and marker dissolved in NSB spotting buffer at the final concentration of 50 μM were printed on the NSB9 NHS slides with PersonalArrayerTM16 Microarray Spotter (CapitalBio, China). ..

MicroChIP Assay:

Article Title: Identification and Validation of Novel Serum Autoantibody Biomarkers for Early Detection of Colorectal Cancer and Advanced Adenoma
Article Snippet: .. Briefly, the screened TAAs were robotically spotted in ordered arrays on aldehyde-activated glass slides by the microchip-spotting instrument PersonalArrayerTM 16 (CapitalBio, Beijing, China). .. Human IgG (Sigma, MO, USA) was spotted by a gradient and used as a positive control and for calibration to adjust the signal intensity of each small compartment, whereas a spot sample of phosphate-buffered saline (PBS) with 0.02% SDS and 1% glycerol, and PBS were used as negative controls.



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Fig. 3. Relative Fluorescence Intensity measured on the spots after the interaction of fluorescently labeled secondary antibody with different AACs (Rabbit IgG-Tag1, Rabbit IgG-Tag2 and Rabbit IgG-Tag3) immobilized on a <t>microarray</t> functionalized with streptavidin (printed at a concentration of 2 mg/mL) and released after incubation with biotin. Blue bars reflect the AAC immobilized on streptavidin, yellow bars represent the AAC left on the spots after biotin-mediated release. Mean ± standard deviation of three independent measurements.
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Fig. 3. Relative Fluorescence Intensity measured on the spots after the interaction of fluorescently labeled secondary antibody with different AACs (Rabbit IgG-Tag1, Rabbit IgG-Tag2 and Rabbit IgG-Tag3) immobilized on a <t>microarray</t> functionalized with streptavidin (printed at a concentration of 2 mg/mL) and released after incubation with biotin. Blue bars reflect the AAC immobilized on streptavidin, yellow bars represent the AAC left on the spots after biotin-mediated release. Mean ± standard deviation of three independent measurements.
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Fig. 3. Relative Fluorescence Intensity measured on the spots after the interaction of fluorescently labeled secondary antibody with different AACs (Rabbit IgG-Tag1, Rabbit IgG-Tag2 and Rabbit IgG-Tag3) immobilized on a microarray functionalized with streptavidin (printed at a concentration of 2 mg/mL) and released after incubation with biotin. Blue bars reflect the AAC immobilized on streptavidin, yellow bars represent the AAC left on the spots after biotin-mediated release. Mean ± standard deviation of three independent measurements.

Journal: Sensors and Actuators B: Chemical

Article Title: Sequential separation and profiling of extracellular vesicles using antibody-aptamer conjugates

doi: 10.1016/j.snb.2024.136939

Figure Lengend Snippet: Fig. 3. Relative Fluorescence Intensity measured on the spots after the interaction of fluorescently labeled secondary antibody with different AACs (Rabbit IgG-Tag1, Rabbit IgG-Tag2 and Rabbit IgG-Tag3) immobilized on a microarray functionalized with streptavidin (printed at a concentration of 2 mg/mL) and released after incubation with biotin. Blue bars reflect the AAC immobilized on streptavidin, yellow bars represent the AAC left on the spots after biotin-mediated release. Mean ± standard deviation of three independent measurements.

Article Snippet: Supports were spotted using a noncontact microarray spotter (sciFLEXARRAYER S12, Scienion, Berlin) equipped with an 80 μm nozzle.

Techniques: Fluorescence, Labeling, Microarray, Concentration Assay, Incubation, Standard Deviation

Fig. 4. Sequence-selective recapture on DNA microarray of 3 different AACs previously immobilized on streptavidin coated magnetic beads and released upon incubation with biotin. Bars represent the Relative Fluorescence Intensity measured on the spots after the interaction of fluorescently labeled secondary antibody with different AACs. Mean ± standard deviation of three independent measurements.

Journal: Sensors and Actuators B: Chemical

Article Title: Sequential separation and profiling of extracellular vesicles using antibody-aptamer conjugates

doi: 10.1016/j.snb.2024.136939

Figure Lengend Snippet: Fig. 4. Sequence-selective recapture on DNA microarray of 3 different AACs previously immobilized on streptavidin coated magnetic beads and released upon incubation with biotin. Bars represent the Relative Fluorescence Intensity measured on the spots after the interaction of fluorescently labeled secondary antibody with different AACs. Mean ± standard deviation of three independent measurements.

Article Snippet: Supports were spotted using a noncontact microarray spotter (sciFLEXARRAYER S12, Scienion, Berlin) equipped with an 80 μm nozzle.

Techniques: Sequencing, Microarray, Magnetic Beads, Incubation, Fluorescence, Labeling, Standard Deviation

Fig. 5. Detection of EVs by label free interferometry separated and recaptured on DNA microarray using antiCD9-Tag2 (red bars). In the negative control, AAC- functionalized magnetic beads were incubated only with PBS-M (blue bars). Mean ± standard deviation of three independent measurements.

Journal: Sensors and Actuators B: Chemical

Article Title: Sequential separation and profiling of extracellular vesicles using antibody-aptamer conjugates

doi: 10.1016/j.snb.2024.136939

Figure Lengend Snippet: Fig. 5. Detection of EVs by label free interferometry separated and recaptured on DNA microarray using antiCD9-Tag2 (red bars). In the negative control, AAC- functionalized magnetic beads were incubated only with PBS-M (blue bars). Mean ± standard deviation of three independent measurements.

Article Snippet: Supports were spotted using a noncontact microarray spotter (sciFLEXARRAYER S12, Scienion, Berlin) equipped with an 80 μm nozzle.

Techniques: Microarray, Negative Control, Magnetic Beads, Incubation, Standard Deviation

Fig. 6. Schematic representation of recapture experiment on ExoView R100 (upper panel) and relative high resolution close ups of a Probe2 spot throughout experimental stages (bottom panel). From left to the right it can be seen i) the surface of the DNA spot, ii) label free interferometry picture of EVs captured on the same spot, and iii) red and green fluorescence picture of the same spot after incubation with labeled antibodies. The bar graphs represent label free interferometric and fluorescent detection of EVs on DNA microarray after separation using streptavidin coated magnetic beads: (b) functionalized with antiCD9-Tag2; (c) func- tionalized with Rabbit IgG-Tag2; (d) non functionalized with AACs. As additional negative control, detection of plasma added with antiCD9-Tag2 without previous separation of EVs on magnetic beads (e). Mean ± standard deviation of three independent measurements.

Journal: Sensors and Actuators B: Chemical

Article Title: Sequential separation and profiling of extracellular vesicles using antibody-aptamer conjugates

doi: 10.1016/j.snb.2024.136939

Figure Lengend Snippet: Fig. 6. Schematic representation of recapture experiment on ExoView R100 (upper panel) and relative high resolution close ups of a Probe2 spot throughout experimental stages (bottom panel). From left to the right it can be seen i) the surface of the DNA spot, ii) label free interferometry picture of EVs captured on the same spot, and iii) red and green fluorescence picture of the same spot after incubation with labeled antibodies. The bar graphs represent label free interferometric and fluorescent detection of EVs on DNA microarray after separation using streptavidin coated magnetic beads: (b) functionalized with antiCD9-Tag2; (c) func- tionalized with Rabbit IgG-Tag2; (d) non functionalized with AACs. As additional negative control, detection of plasma added with antiCD9-Tag2 without previous separation of EVs on magnetic beads (e). Mean ± standard deviation of three independent measurements.

Article Snippet: Supports were spotted using a noncontact microarray spotter (sciFLEXARRAYER S12, Scienion, Berlin) equipped with an 80 μm nozzle.

Techniques: Fluorescence, Incubation, Labeling, Microarray, Magnetic Beads, Negative Control, Clinical Proteomics, Standard Deviation

Fig. 8. Recapture and multiplexed detection on DNA microarray of EVs sepa- rated using antiCD9-Tag2 immobilized on magnetic beads and labeled using antiCD63-Tag1. Mean ± standard deviation of three independent measurements.

Journal: Sensors and Actuators B: Chemical

Article Title: Sequential separation and profiling of extracellular vesicles using antibody-aptamer conjugates

doi: 10.1016/j.snb.2024.136939

Figure Lengend Snippet: Fig. 8. Recapture and multiplexed detection on DNA microarray of EVs sepa- rated using antiCD9-Tag2 immobilized on magnetic beads and labeled using antiCD63-Tag1. Mean ± standard deviation of three independent measurements.

Article Snippet: Supports were spotted using a noncontact microarray spotter (sciFLEXARRAYER S12, Scienion, Berlin) equipped with an 80 μm nozzle.

Techniques: Microarray, Magnetic Beads, Labeling, Standard Deviation