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SCHOTT microarray slides
Microarray Slides, 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/microarray+slide/microarray+slides/pmc06769450-81-18-21
Average 90 stars, based on 1 article reviews
microarray slides - by Bioz Stars, 2026-10
90/100 stars

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Related Articles

Binding Assay:

Article Title: A Neutralizing Antibody Recognizing Primarily N -linked Glycan Targets the Silent Face of the HIV Envelope
Article Snippet: .. While we did not observe VRC-PG05 binding under standard conditions to NHS (Nexterion H, SCHOTT) microarray slides coated with 40 N-glycans, when assessed at higher ionic strength (10×PBS) ( Chen et al., 2017 ), VRC-PG05 exhibited specific binding to Man 9 (#6 glycan) ( Figure S3E ). ..

Microarray:

Article Title: A Neutralizing Antibody Recognizing Primarily N -linked Glycan Targets the Silent Face of the HIV Envelope
Article Snippet: .. While we did not observe VRC-PG05 binding under standard conditions to NHS (Nexterion H, SCHOTT) microarray slides coated with 40 N-glycans, when assessed at higher ionic strength (10×PBS) ( Chen et al., 2017 ), VRC-PG05 exhibited specific binding to Man 9 (#6 glycan) ( Figure S3E ). ..

Article Title: Altered Levels of Toll-Like Receptors in Circulating Extracellular Vesicles in Multiple Sclerosis
Article Snippet: .. Micro-sized spots of 40 different capturing antibodies (200 μg/mL) against known EV surface antigens were printed on standard epoxysilane-coated microarray slides (SCHOTT Nexterion, Germany) using a SpotBot ® Extreme Protein Edition Microarray Printer (ArrayIt Corporation, CA, U.S.). ..

Article Title: MicroRNAs expression signature for determination of tumors origin
Article Snippet: .. 20 μM of each probe were dissolved in 2×SSC+0.0035% SDS and spotted in triplicate on Slide E coated microarray slides (Schott Nexterion, Mainz, Germany) using the BioRobotics MicroGrid II microarrater (Genomic Solutions, Ann Arbor, Mich.) according to the manufacturer's directions. ..

Article Title: Age-Dependent Glycomic Response to the 2009 Pandemic H1N1 Influenza Virus and Its Association with Disease Severity
Article Snippet: .. Immobilization Surface; e.g., Microarray Slide S23 Immobilization surface Nexterion Slide H Barcoded 3D Hydrogel Coated Manufacturer Schott North America Custom preparation of surface N/A .. Description of Arrayer Nano-Plotter 2.1 piezoelectric printer (GeSim, Germany) with cooled microwell plate holder and cooled printing deck Lectin deposition Three replicates of each lectin are printed onto each subarray.

Article Title: Methods of identifying glycopeptides recognized by disease-associated auto-antibodies
Article Snippet: .. A total of 960 GalNAc glycopeptides were synthesized at 0.5 mg scale (Sigma) and printed on microarray hydrogel slides (Schott Nexterion) as described in Example 1. .. A total of 960 GalNAc glycopeptides were synthesized at 0.5 mg scale (Sigma) and printed on microarray hydrogel slides (Schott Nexterion) as described in Example 1.

Article Title: Fabrication of DNA Microarrays on Polydopamine-Modified Gold Thin Films for SPR Imaging Measurements
Article Snippet: Materials Polydopamine (PDA) coating was performed using dopamine hydrochloride (Sigma-Aldrich) dissolved in 10 mM Tris buffer (Trizma hydrochloride; Sigma-Aldrich) at pH 8.5. .. Microarray chips (16 spots, 1.0 mm diameter) for SPR imaging experiments were prepared by thermally evaporating (Denton DV 502-A evaporator) 45 nm of gold, with 1 nm of chromium underneath as an adhesion layer, onto SF10 glass slides (18 × 18 mm; Schott Glass). .. Nucleic Acids Modified ssDNA oligonucleotides (Integrated DNA Technologies) were diluted in either 1X phosphate buffer (11.9 mM phosphates, 137 mM sodium chloride, 2.7 mM potassium chloride, pH 7.4; Fisher) for DNA hybridization and AuNP modification, or Tris buffer for ssDNA fabrication onto the PDA layer.

Glycoproteomics:

Article Title: A Neutralizing Antibody Recognizing Primarily N -linked Glycan Targets the Silent Face of the HIV Envelope
Article Snippet: .. While we did not observe VRC-PG05 binding under standard conditions to NHS (Nexterion H, SCHOTT) microarray slides coated with 40 N-glycans, when assessed at higher ionic strength (10×PBS) ( Chen et al., 2017 ), VRC-PG05 exhibited specific binding to Man 9 (#6 glycan) ( Figure S3E ). ..

other:

Article Title: Absence of a human ortholog of rodent Kupffer cell galactose-binding receptor encoded by the CLEC4f gene
Article Snippet: Oligosaccharide arrays immobilized on glass slides were from the Consortium for Functional Glycomics (Versions 2.1 and 6.2) with six replicates printed on NHS-activated microarray slides (SlideH, Schott/Nexterion) using a contact printer ( ).

Synthesized:

Article Title: Methods of identifying glycopeptides recognized by disease-associated auto-antibodies
Article Snippet: .. A total of 960 GalNAc glycopeptides were synthesized at 0.5 mg scale (Sigma) and printed on microarray hydrogel slides (Schott Nexterion) as described in Example 1. .. A total of 960 GalNAc glycopeptides were synthesized at 0.5 mg scale (Sigma) and printed on microarray hydrogel slides (Schott Nexterion) as described in Example 1.

SPR Assay:

Article Title: Fabrication of DNA Microarrays on Polydopamine-Modified Gold Thin Films for SPR Imaging Measurements
Article Snippet: Materials Polydopamine (PDA) coating was performed using dopamine hydrochloride (Sigma-Aldrich) dissolved in 10 mM Tris buffer (Trizma hydrochloride; Sigma-Aldrich) at pH 8.5. .. Microarray chips (16 spots, 1.0 mm diameter) for SPR imaging experiments were prepared by thermally evaporating (Denton DV 502-A evaporator) 45 nm of gold, with 1 nm of chromium underneath as an adhesion layer, onto SF10 glass slides (18 × 18 mm; Schott Glass). .. Nucleic Acids Modified ssDNA oligonucleotides (Integrated DNA Technologies) were diluted in either 1X phosphate buffer (11.9 mM phosphates, 137 mM sodium chloride, 2.7 mM potassium chloride, pH 7.4; Fisher) for DNA hybridization and AuNP modification, or Tris buffer for ssDNA fabrication onto the PDA layer.

Imaging:

Article Title: Fabrication of DNA Microarrays on Polydopamine-Modified Gold Thin Films for SPR Imaging Measurements
Article Snippet: Materials Polydopamine (PDA) coating was performed using dopamine hydrochloride (Sigma-Aldrich) dissolved in 10 mM Tris buffer (Trizma hydrochloride; Sigma-Aldrich) at pH 8.5. .. Microarray chips (16 spots, 1.0 mm diameter) for SPR imaging experiments were prepared by thermally evaporating (Denton DV 502-A evaporator) 45 nm of gold, with 1 nm of chromium underneath as an adhesion layer, onto SF10 glass slides (18 × 18 mm; Schott Glass). .. Nucleic Acids Modified ssDNA oligonucleotides (Integrated DNA Technologies) were diluted in either 1X phosphate buffer (11.9 mM phosphates, 137 mM sodium chloride, 2.7 mM potassium chloride, pH 7.4; Fisher) for DNA hybridization and AuNP modification, or Tris buffer for ssDNA fabrication onto the PDA layer.



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Mean <t>microarray</t> antigen spot intensities from TB-free badger serum samples at two time points following experimental infection. White bars represent TB-free sera; gray bars represent TB-infected sera collected at ( a ) 8 weeks and ( b ) 12–13 weeks post-infection. Mean microarray spot intensities (log 2 -normalized) are shown with 95% confidence interval error bars. Paired-sample t -tests were carried out comparing pre- and post-infection mean spot intensities. Antigens were ranked by BH-adjusted P -values, and the 10 most differential antigens (defined as those with the lowest BH-adjusted P -values) for each comparison group are shown. Significance levels: ns: P ≥ 0.05; *: P < 0.05; **: P < 0.01; and ***: P < 0.001.
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Mean <t>microarray</t> antigen spot intensities from TB-free badger serum samples at two time points following experimental infection. White bars represent TB-free sera; gray bars represent TB-infected sera collected at ( a ) 8 weeks and ( b ) 12–13 weeks post-infection. Mean microarray spot intensities (log 2 -normalized) are shown with 95% confidence interval error bars. Paired-sample t -tests were carried out comparing pre- and post-infection mean spot intensities. Antigens were ranked by BH-adjusted P -values, and the 10 most differential antigens (defined as those with the lowest BH-adjusted P -values) for each comparison group are shown. Significance levels: ns: P ≥ 0.05; *: P < 0.05; **: P < 0.01; and ***: P < 0.001.
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Image Search Results


Mean microarray antigen spot intensities from TB-free badger serum samples at two time points following experimental infection. White bars represent TB-free sera; gray bars represent TB-infected sera collected at ( a ) 8 weeks and ( b ) 12–13 weeks post-infection. Mean microarray spot intensities (log 2 -normalized) are shown with 95% confidence interval error bars. Paired-sample t -tests were carried out comparing pre- and post-infection mean spot intensities. Antigens were ranked by BH-adjusted P -values, and the 10 most differential antigens (defined as those with the lowest BH-adjusted P -values) for each comparison group are shown. Significance levels: ns: P ≥ 0.05; *: P < 0.05; **: P < 0.01; and ***: P < 0.001.

Journal: Journal of Clinical Microbiology

Article Title: Proteome microarray-guided identification of mycobacterial antigens and ELISA-based peptide mapping for improved serological detection of Mycobacterium bovis infection in European badgers

doi: 10.1128/jcm.01260-25

Figure Lengend Snippet: Mean microarray antigen spot intensities from TB-free badger serum samples at two time points following experimental infection. White bars represent TB-free sera; gray bars represent TB-infected sera collected at ( a ) 8 weeks and ( b ) 12–13 weeks post-infection. Mean microarray spot intensities (log 2 -normalized) are shown with 95% confidence interval error bars. Paired-sample t -tests were carried out comparing pre- and post-infection mean spot intensities. Antigens were ranked by BH-adjusted P -values, and the 10 most differential antigens (defined as those with the lowest BH-adjusted P -values) for each comparison group are shown. Significance levels: ns: P ≥ 0.05; *: P < 0.05; **: P < 0.01; and ***: P < 0.001.

Article Snippet: Translated proteins and IVTT controls were printed onto custom nitrocellulose-coated microarray slides (Grace Bio-Labs, Bend, OR, USA) using a GeneMachines OmniGrid Accent Microarray Printer.

Techniques: Microarray, Infection, Comparison

Mean microarray antigen spot intensities from TB-infected and BCG-vaccinated badger serum samples. Gray bars represent sera from TB-infected badgers collected 12–13 weeks after experimental infection; white bars represent sera from badgers that received ( a ) a single BCG vaccination or ( b ) two BCG vaccinations. Mean spot intensities (log₂-normalized) are shown with 95% confidence interval error bars. Independent-samples t -tests were used to compare antigen intensities between TB-infected and BCG-vaccinated groups. Antigens were ranked by BH-adjusted P -values, and the 10 most differential antigens (defined as those with the lowest BH-adjusted P -values) for each comparison group are shown; ***: P < 0.001.

Journal: Journal of Clinical Microbiology

Article Title: Proteome microarray-guided identification of mycobacterial antigens and ELISA-based peptide mapping for improved serological detection of Mycobacterium bovis infection in European badgers

doi: 10.1128/jcm.01260-25

Figure Lengend Snippet: Mean microarray antigen spot intensities from TB-infected and BCG-vaccinated badger serum samples. Gray bars represent sera from TB-infected badgers collected 12–13 weeks after experimental infection; white bars represent sera from badgers that received ( a ) a single BCG vaccination or ( b ) two BCG vaccinations. Mean spot intensities (log₂-normalized) are shown with 95% confidence interval error bars. Independent-samples t -tests were used to compare antigen intensities between TB-infected and BCG-vaccinated groups. Antigens were ranked by BH-adjusted P -values, and the 10 most differential antigens (defined as those with the lowest BH-adjusted P -values) for each comparison group are shown; ***: P < 0.001.

Article Snippet: Translated proteins and IVTT controls were printed onto custom nitrocellulose-coated microarray slides (Grace Bio-Labs, Bend, OR, USA) using a GeneMachines OmniGrid Accent Microarray Printer.

Techniques: Microarray, Infection, Comparison