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3d-amino glass slides  (PolyAn GmbH)


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    Structured Review

    PolyAn GmbH 3d-amino glass slides
    3d Amino Glass Slides, supplied by PolyAn GmbH, 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/3d+amine+microarray+slide/pmc08589469-38-34-46
    Average 90 stars, based on 1 article reviews
    3d-amino glass slides - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Glycoproteomics:

    Article Title: Method and device for producing saccharides and saccharide arrays
    Article Snippet: .. 2.1 Acceptor slide preparation: The vapor triggered glycosylation reaction of a glycosyl donor and a glycosyl acceptor on a functionalized glass slide (solid support) was accomplished on a commercially available 3D amine microarray slide from PolyAn GmbH (Berlin). ..

    Article Title: Method and device for producing saccharides and saccharide arrays
    Article Snippet: .. To perform the glycosylation method—the glycosylation on a solid support using vapor—the 3D amine microarray slide from PolyAn GmbH (Berlin) was functionalized for this purpose. .. Therefore, first the commercially available (Iris Biotech GmbH, Marktredwitz) photocleavable linker 2a were attached on the slide, followed by spacer 4 and finally by modified galactose building block 6 (FIG. 10).

    Microarray:

    Article Title: Method and device for producing saccharides and saccharide arrays
    Article Snippet: .. 2.1 Acceptor slide preparation: The vapor triggered glycosylation reaction of a glycosyl donor and a glycosyl acceptor on a functionalized glass slide (solid support) was accomplished on a commercially available 3D amine microarray slide from PolyAn GmbH (Berlin). ..

    Article Title: Method and device for producing saccharides and saccharide arrays
    Article Snippet: .. To perform the glycosylation method—the glycosylation on a solid support using vapor—the 3D amine microarray slide from PolyAn GmbH (Berlin) was functionalized for this purpose. .. Therefore, first the commercially available (Iris Biotech GmbH, Marktredwitz) photocleavable linker 2a were attached on the slide, followed by spacer 4 and finally by modified galactose building block 6 (FIG. 10).

    other:

    Article Title: Probing Multivalent Carbohydrate-Protein Interactions With On-Chip Synthesized Glycopeptides Using Different Functionalized Surfaces
    Article Snippet: Fmoc-NH-β-Ala-PEGMA-co-MMA glass slides (∼20 nm thick coating, loading of functional groups according to vendor 1 nmol cm −2 , estimated functional group spacing of 7–10 nm) were acquired from PEPperPRINT GmbH (Germany) and the 3D-Amino glass slides (according to vendor 1–5 nmol cm −2 ) from PolyAn GmbH (Germany).

    Article Title: VaporLIFT: On‐Chip Chemical Synthesis of Glycan Microarrays
    Article Snippet: Acceptor Slide: The 3D-Amino glass slides (according to vendor 1– 5 nmol cm−1) were obtained from PolyAn GmbH, Berlin, Germany.

    Article Title: Surface regeneration of microfluidic microarray printheads through plasma techniques
    Article Snippet: This work describes a method for surface regeneration of microfluidic microarray printheads through plasma techniques.. Modification procedures were chosen in a way to obtain high reproducibility with a minimum of time consumption.. The idea behind this is a complete regeneration of a microarray printhead before or after usage to achieve best printing results over a typical print job.

    Functional Assay:

    Article Title: Probing Multivalent Carbohydrate-Protein Interactions With On-Chip Synthesized Glycopeptides Using Different Functionalized Surfaces.
    Article Snippet: .. Fmoc-NH-β-Ala-PEGMA-co-MMA glass slides (∼20 nm thick coating, loading of functional groups according to vendor 1 nmol cm−2, estimated functional group spacing of 7–10 nm) were acquired from PEPperPRINT GmbH (Germany) and the 3DAmino glass slides (according to vendor 1–5 nmol cm−2) from PolyAn GmbH (Germany). .. On PolyAn and PEPperPRINT slides, Frontiers in Chemistry | www.frontiersin.org October 2021 | Volume 9 | Article 7669322 a hydrophilic PEG ((EG)3) -based spacer (≈17 Å length) was attached (see Supplementary Material, Section 3.2), before the synthesis of the desired tetrapeptides.



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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