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high binding plates  (Greiner Bio)


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    Greiner Bio high binding plates
    High Binding Plates, supplied by Greiner Bio, used in various techniques. Bioz Stars score: 97/100, based on 620 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/high+binding+microplate/Microplate+96+Well+Ps+F-Bottom/pm41861097-53-3-6
    Average 97 stars, based on 620 article reviews
    high binding plates - by Bioz Stars, 2026-11
    97/100 stars

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    Related Articles

    Software:

    Article Title: A pericyte-to-myofibroblast transition links APOE4 to cerebrovascular degeneration.
    Article Snippet: .. Fgsea (v1.28.0) Korotkevich et al.123 https://github.com/alserglab/fgsea Fiji (v2.3.0) Schindelin et al.124 imagej.net/software/fiji/ GraphPad Prism (v10.4.1) GraphPad Software graphpad.com GSVA (v1.50.5) Hänzelmann et al.125 https://github.com/rcastelo/GSVA Harmony (v1.2.3) Korsunsky et al.126 https://github.com/immunogenomics/ harmony Limma (v3.58.1) Ritchie et al.127 https://bioconductor.org/packages/ release/bioc/html/limma.html MAST (v1.28.0) Finak et al.128 https://github.com/RGLab/MAST Mgcv (v1.9.3) Wood129 https://cran.r-project.org/web/ packages/mgcv/index.html miloR (v1.10.0) Dann et al.41 https://github.com/MarioniLab/miloR Msigdbr (v10.0.2) Dolgalev130 https://igordot.github.io/msigdbr/ NicheNet (v2.1.5) Broweays et al.71 https://github.com/saeyslab/nichenetr Nikon NIS Elements software Nikon microscope.healthcare.nikon.com Python (v3.13.5) Python https://www.python.org R (v4.3.2) R Project https://www.r-project.org/ R Studio (v2024.04.2) Posit https://posit.co/download/ rstudio-desktop/ Scanpy (v1.11.4) Wolf et al.131 https://pypi.org/project/scanpy/ Seurat (v5.2.1) Hao et al.132 https://satijalab.org/seurat/ Slingshot (v2.10.0) Street et al.133 https://github.com/kstreet13/slingshot Other 96-well plate with cover glass thickness polystyrene bottom Greiner Bio-One Cat# 655096 Ti2E Ax R Confocal Microscope Nikon microscope.healthcare.nikon.com ll e4 Cell 189, 1–20.e1–e13, November 25, 2026 Article ..

    Microscopy:

    Article Title: A pericyte-to-myofibroblast transition links APOE4 to cerebrovascular degeneration.
    Article Snippet: .. Fgsea (v1.28.0) Korotkevich et al.123 https://github.com/alserglab/fgsea Fiji (v2.3.0) Schindelin et al.124 imagej.net/software/fiji/ GraphPad Prism (v10.4.1) GraphPad Software graphpad.com GSVA (v1.50.5) Hänzelmann et al.125 https://github.com/rcastelo/GSVA Harmony (v1.2.3) Korsunsky et al.126 https://github.com/immunogenomics/ harmony Limma (v3.58.1) Ritchie et al.127 https://bioconductor.org/packages/ release/bioc/html/limma.html MAST (v1.28.0) Finak et al.128 https://github.com/RGLab/MAST Mgcv (v1.9.3) Wood129 https://cran.r-project.org/web/ packages/mgcv/index.html miloR (v1.10.0) Dann et al.41 https://github.com/MarioniLab/miloR Msigdbr (v10.0.2) Dolgalev130 https://igordot.github.io/msigdbr/ NicheNet (v2.1.5) Broweays et al.71 https://github.com/saeyslab/nichenetr Nikon NIS Elements software Nikon microscope.healthcare.nikon.com Python (v3.13.5) Python https://www.python.org R (v4.3.2) R Project https://www.r-project.org/ R Studio (v2024.04.2) Posit https://posit.co/download/ rstudio-desktop/ Scanpy (v1.11.4) Wolf et al.131 https://pypi.org/project/scanpy/ Seurat (v5.2.1) Hao et al.132 https://satijalab.org/seurat/ Slingshot (v2.10.0) Street et al.133 https://github.com/kstreet13/slingshot Other 96-well plate with cover glass thickness polystyrene bottom Greiner Bio-One Cat# 655096 Ti2E Ax R Confocal Microscope Nikon microscope.healthcare.nikon.com ll e4 Cell 189, 1–20.e1–e13, November 25, 2026 Article ..

    Glass:

    Article Title: A pericyte-to-myofibroblast transition links APOE4 to cerebrovascular degeneration.
    Article Snippet: .. Fgsea (v1.28.0) Korotkevich et al.123 https://github.com/alserglab/fgsea Fiji (v2.3.0) Schindelin et al.124 imagej.net/software/fiji/ GraphPad Prism (v10.4.1) GraphPad Software graphpad.com GSVA (v1.50.5) Hänzelmann et al.125 https://github.com/rcastelo/GSVA Harmony (v1.2.3) Korsunsky et al.126 https://github.com/immunogenomics/ harmony Limma (v3.58.1) Ritchie et al.127 https://bioconductor.org/packages/ release/bioc/html/limma.html MAST (v1.28.0) Finak et al.128 https://github.com/RGLab/MAST Mgcv (v1.9.3) Wood129 https://cran.r-project.org/web/ packages/mgcv/index.html miloR (v1.10.0) Dann et al.41 https://github.com/MarioniLab/miloR Msigdbr (v10.0.2) Dolgalev130 https://igordot.github.io/msigdbr/ NicheNet (v2.1.5) Broweays et al.71 https://github.com/saeyslab/nichenetr Nikon NIS Elements software Nikon microscope.healthcare.nikon.com Python (v3.13.5) Python https://www.python.org R (v4.3.2) R Project https://www.r-project.org/ R Studio (v2024.04.2) Posit https://posit.co/download/ rstudio-desktop/ Scanpy (v1.11.4) Wolf et al.131 https://pypi.org/project/scanpy/ Seurat (v5.2.1) Hao et al.132 https://satijalab.org/seurat/ Slingshot (v2.10.0) Street et al.133 https://github.com/kstreet13/slingshot Other 96-well plate with cover glass thickness polystyrene bottom Greiner Bio-One Cat# 655096 Ti2E Ax R Confocal Microscope Nikon microscope.healthcare.nikon.com ll e4 Cell 189, 1–20.e1–e13, November 25, 2026 Article ..

    Confocal:

    Article Title: A pericyte-to-myofibroblast transition links APOE4 to cerebrovascular degeneration.
    Article Snippet: .. Fgsea (v1.28.0) Korotkevich et al.123 https://github.com/alserglab/fgsea Fiji (v2.3.0) Schindelin et al.124 imagej.net/software/fiji/ GraphPad Prism (v10.4.1) GraphPad Software graphpad.com GSVA (v1.50.5) Hänzelmann et al.125 https://github.com/rcastelo/GSVA Harmony (v1.2.3) Korsunsky et al.126 https://github.com/immunogenomics/ harmony Limma (v3.58.1) Ritchie et al.127 https://bioconductor.org/packages/ release/bioc/html/limma.html MAST (v1.28.0) Finak et al.128 https://github.com/RGLab/MAST Mgcv (v1.9.3) Wood129 https://cran.r-project.org/web/ packages/mgcv/index.html miloR (v1.10.0) Dann et al.41 https://github.com/MarioniLab/miloR Msigdbr (v10.0.2) Dolgalev130 https://igordot.github.io/msigdbr/ NicheNet (v2.1.5) Broweays et al.71 https://github.com/saeyslab/nichenetr Nikon NIS Elements software Nikon microscope.healthcare.nikon.com Python (v3.13.5) Python https://www.python.org R (v4.3.2) R Project https://www.r-project.org/ R Studio (v2024.04.2) Posit https://posit.co/download/ rstudio-desktop/ Scanpy (v1.11.4) Wolf et al.131 https://pypi.org/project/scanpy/ Seurat (v5.2.1) Hao et al.132 https://satijalab.org/seurat/ Slingshot (v2.10.0) Street et al.133 https://github.com/kstreet13/slingshot Other 96-well plate with cover glass thickness polystyrene bottom Greiner Bio-One Cat# 655096 Ti2E Ax R Confocal Microscope Nikon microscope.healthcare.nikon.com ll e4 Cell 189, 1–20.e1–e13, November 25, 2026 Article ..

    Saline:

    Article Title: Rate of osmotic pressure change in drying saliva microdroplets drives inactivation of model respiratory bacteria.
    Article Snippet: .. Once the chamber was ready, 1 μL droplets of artificial saliva (Pickering Laboratories) or phosphate-buffered saline (PBS; Gibco) containing 108 colony-forming units per mL of E. coli or S. epidermidis were deposited into a 96-well plate with non-binding surfaces (Greiner Bio-One, 655901), with one droplet Month XXXX Volume 0 Issue 0 10.1128/msphere.00594-2610 h ttp s: //j ou rn al s. as m .o rg /jo ur na l/m sp he re o n 19 O ct ob er 2 02 6 by 2 80 4: 1b 3: a9 00 :5 20 6: d4 06 :e 23 a: ed 9: 60 6c ..

    other:

    Article Title: Detection of transition metal ions, odorous compounds and wastewater in river water using a reaction-based optical fingerprinting strategy.
    Article Snippet: Although water quality monitoring using optical sensors has been extensively studied, it remains a frontline research area owing to its simplicity and adaptability.. In this study, we continue to develop a kinetic-based sensing strategy based on multiple optical measurements during an indicator reaction.. The effect on the reaction rate makes it possible to observe the effect of sample components that do not otherwise manifest themselves in photometry and fluorimetry.

    Binding Assay:

    Article Title: Design and validation of a GMP-compliant manufacturing platform of extracellular vesicles from mesenchymal stromal cells
    Article Snippet: Protein LoBind Tubes , Eppendorf , 22431081. .. 96-well plate, flat bottom, low binding , Greiner , 655901. .. Transfer bags (150 mL - 2 L) , Fresenius Kabi , 4R20XX series.

    Fluorescence:

    Article Title: Distinct A β 40 and A β 42 co-assembly pathways with free lipids: Experiment-driven MD study †
    Article Snippet: .. ThT fluorescence measurements are performed in Greiner Bio-One 96-well microplates (655900) using a FLUOstar Omega microplate reader (BMG LABTECH) at room temperature, with excitation at 448 nm and emission at 480 nm. ..

    Enzyme-linked Immunosorbent Assay:

    Article Title: Symmetric Dimethylarginine Modification Drives Shared and Divergent Antigen Reactivity in Lupus
    Article Snippet: .. High-binding ELISA plates (Greiner Bio-One, 655081) were coated with 250 ng/well of streptavidin (Leinco Technologies, S203) overnight at 4°C. ..



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    (A) Sera from MRL lpr mice (n=12, bled weekly from 8 to 13 weeks of age) were analyzed by <t>ELISA</t> using synthetic 10×RG peptides: native sequence (GRGRGRGRGRGRGRGRGRGR) vs. SDMA-modified (lowercase ‘r’ denotes SDMA; GrGrGrGRGRGrGrGrGRGR). All 12 mice developed anti SDMA antibody titers above the corresponding native controls, and the majority (9/12) showed a gradual increase in anti-SDMA titers over time. (B) Immunoblotting of HEp-2 lysates revealed progressive changes in band patterns from 10 weeks onward. To identify SDMA specific reactive proteins, cells were pretreated with the methyltransferase inhibitor EPZ015666 (EPZ) before lysis. A prominent ∼15 kDa band (arrowhead) was markedly reduced by EPZ pretreatment, supporting its recognition by anti SDMA antibodies. (C) Sera from three 12 week old MRL lpr littermates (Lpr 1, 2, 3) each showed distinct band patterns against the cell lysates. EPZ pretreatment of the cells reduced the intensity of several bands in all three mice. (D) Workflow for isolating hybridoma clones from individual plasma cells to obtain monoclonal antibodies (mAbs) specific for SDMA. MRL lpr mice were not immunized with any antigen; thus, the resulting mAbs represent naturally arising autoantibodies. (E) Two antibody clones were tested against the native versus SDMA peptide array shown in Figurè3. Clone P4A2F4 reacted extensively with most SDMA containing peptides, whereas clone P2C1C10 showed no reactivity. (F) The two mAbs produced different band patterns on cell lysates. P4A2F4 recognized bands that were reduced in EPZ pretreated lysates, consistent with SDMA specificity. (G) After implantation of the SDMA-reactive hybridoma clone into the peritoneal cavity of healthy BALB/c mice, the kidneys showed extensive IgG deposition, reminiscent of human lupus nephritis.
    High Binding Elisa Plates, supplied by Greiner Bio, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    (A) Sera from MRL lpr mice (n=12, bled weekly from 8 to 13 weeks of age) were analyzed by <t>ELISA</t> using synthetic 10×RG peptides: native sequence (GRGRGRGRGRGRGRGRGRGR) vs. SDMA-modified (lowercase ‘r’ denotes SDMA; GrGrGrGRGRGrGrGrGRGR). All 12 mice developed anti SDMA antibody titers above the corresponding native controls, and the majority (9/12) showed a gradual increase in anti-SDMA titers over time. (B) Immunoblotting of HEp-2 lysates revealed progressive changes in band patterns from 10 weeks onward. To identify SDMA specific reactive proteins, cells were pretreated with the methyltransferase inhibitor EPZ015666 (EPZ) before lysis. A prominent ∼15 kDa band (arrowhead) was markedly reduced by EPZ pretreatment, supporting its recognition by anti SDMA antibodies. (C) Sera from three 12 week old MRL lpr littermates (Lpr 1, 2, 3) each showed distinct band patterns against the cell lysates. EPZ pretreatment of the cells reduced the intensity of several bands in all three mice. (D) Workflow for isolating hybridoma clones from individual plasma cells to obtain monoclonal antibodies (mAbs) specific for SDMA. MRL lpr mice were not immunized with any antigen; thus, the resulting mAbs represent naturally arising autoantibodies. (E) Two antibody clones were tested against the native versus SDMA peptide array shown in Figurè3. Clone P4A2F4 reacted extensively with most SDMA containing peptides, whereas clone P2C1C10 showed no reactivity. (F) The two mAbs produced different band patterns on cell lysates. P4A2F4 recognized bands that were reduced in EPZ pretreated lysates, consistent with SDMA specificity. (G) After implantation of the SDMA-reactive hybridoma clone into the peritoneal cavity of healthy BALB/c mice, the kidneys showed extensive IgG deposition, reminiscent of human lupus nephritis.
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    Detection of cathelicidin (LL-37) and myeloperoxidase (MPO) in human urine samples. Protein concentrations in human urine samples were detected by ELISA. The samples were analyzed in a <t>microplate</t> reader. Bar represents mean ± SD of each group. Protein levels were compared across groups (A, C) and subgroups (B, D). (A, C) LL-37 and MPO concentrations are higher in infected (Group A and B) than in healthy urines (Control). (B, D) No difference in protein concentrations was found when comparing the subgroups of Group A. ****p < 0.0001.
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    Detection of cathelicidin (LL-37) and myeloperoxidase (MPO) in human urine samples. Protein concentrations in human urine samples were detected by ELISA. The samples were analyzed in a <t>microplate</t> reader. Bar represents mean ± SD of each group. Protein levels were compared across groups (A, C) and subgroups (B, D). (A, C) LL-37 and MPO concentrations are higher in infected (Group A and B) than in healthy urines (Control). (B, D) No difference in protein concentrations was found when comparing the subgroups of Group A. ****p < 0.0001.
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    high binding microplate  (Greiner Bio)
    95
    Greiner Bio high binding microplate
    Detection of cathelicidin (LL-37) and myeloperoxidase (MPO) in human urine samples. Protein concentrations in human urine samples were detected by ELISA. The samples were analyzed in a <t>microplate</t> reader. Bar represents mean ± SD of each group. Protein levels were compared across groups (A, C) and subgroups (B, D). (A, C) LL-37 and MPO concentrations are higher in infected (Group A and B) than in healthy urines (Control). (B, D) No difference in protein concentrations was found when comparing the subgroups of Group A. ****p < 0.0001.
    High Binding Microplate, supplied by Greiner Bio, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    (A) Sera from MRL lpr mice (n=12, bled weekly from 8 to 13 weeks of age) were analyzed by ELISA using synthetic 10×RG peptides: native sequence (GRGRGRGRGRGRGRGRGRGR) vs. SDMA-modified (lowercase ‘r’ denotes SDMA; GrGrGrGRGRGrGrGrGRGR). All 12 mice developed anti SDMA antibody titers above the corresponding native controls, and the majority (9/12) showed a gradual increase in anti-SDMA titers over time. (B) Immunoblotting of HEp-2 lysates revealed progressive changes in band patterns from 10 weeks onward. To identify SDMA specific reactive proteins, cells were pretreated with the methyltransferase inhibitor EPZ015666 (EPZ) before lysis. A prominent ∼15 kDa band (arrowhead) was markedly reduced by EPZ pretreatment, supporting its recognition by anti SDMA antibodies. (C) Sera from three 12 week old MRL lpr littermates (Lpr 1, 2, 3) each showed distinct band patterns against the cell lysates. EPZ pretreatment of the cells reduced the intensity of several bands in all three mice. (D) Workflow for isolating hybridoma clones from individual plasma cells to obtain monoclonal antibodies (mAbs) specific for SDMA. MRL lpr mice were not immunized with any antigen; thus, the resulting mAbs represent naturally arising autoantibodies. (E) Two antibody clones were tested against the native versus SDMA peptide array shown in Figurè3. Clone P4A2F4 reacted extensively with most SDMA containing peptides, whereas clone P2C1C10 showed no reactivity. (F) The two mAbs produced different band patterns on cell lysates. P4A2F4 recognized bands that were reduced in EPZ pretreated lysates, consistent with SDMA specificity. (G) After implantation of the SDMA-reactive hybridoma clone into the peritoneal cavity of healthy BALB/c mice, the kidneys showed extensive IgG deposition, reminiscent of human lupus nephritis.

    Journal: bioRxiv

    Article Title: Symmetric Dimethylarginine Modification Drives Shared and Divergent Antigen Reactivity in Lupus

    doi: 10.64898/2026.09.22.753525

    Figure Lengend Snippet: (A) Sera from MRL lpr mice (n=12, bled weekly from 8 to 13 weeks of age) were analyzed by ELISA using synthetic 10×RG peptides: native sequence (GRGRGRGRGRGRGRGRGRGR) vs. SDMA-modified (lowercase ‘r’ denotes SDMA; GrGrGrGRGRGrGrGrGRGR). All 12 mice developed anti SDMA antibody titers above the corresponding native controls, and the majority (9/12) showed a gradual increase in anti-SDMA titers over time. (B) Immunoblotting of HEp-2 lysates revealed progressive changes in band patterns from 10 weeks onward. To identify SDMA specific reactive proteins, cells were pretreated with the methyltransferase inhibitor EPZ015666 (EPZ) before lysis. A prominent ∼15 kDa band (arrowhead) was markedly reduced by EPZ pretreatment, supporting its recognition by anti SDMA antibodies. (C) Sera from three 12 week old MRL lpr littermates (Lpr 1, 2, 3) each showed distinct band patterns against the cell lysates. EPZ pretreatment of the cells reduced the intensity of several bands in all three mice. (D) Workflow for isolating hybridoma clones from individual plasma cells to obtain monoclonal antibodies (mAbs) specific for SDMA. MRL lpr mice were not immunized with any antigen; thus, the resulting mAbs represent naturally arising autoantibodies. (E) Two antibody clones were tested against the native versus SDMA peptide array shown in Figurè3. Clone P4A2F4 reacted extensively with most SDMA containing peptides, whereas clone P2C1C10 showed no reactivity. (F) The two mAbs produced different band patterns on cell lysates. P4A2F4 recognized bands that were reduced in EPZ pretreated lysates, consistent with SDMA specificity. (G) After implantation of the SDMA-reactive hybridoma clone into the peritoneal cavity of healthy BALB/c mice, the kidneys showed extensive IgG deposition, reminiscent of human lupus nephritis.

    Article Snippet: High-binding ELISA plates (Greiner Bio-One, 655081) were coated with 250 ng/well of streptavidin (Leinco Technologies, S203) overnight at 4°C.

    Techniques: Enzyme-linked Immunosorbent Assay, Sequencing, Modification, Western Blot, Lysis, Clone Assay, Clinical Proteomics, Bioprocessing, Autoantibodies, Peptide Microarray, Produced

    Detection of cathelicidin (LL-37) and myeloperoxidase (MPO) in human urine samples. Protein concentrations in human urine samples were detected by ELISA. The samples were analyzed in a microplate reader. Bar represents mean ± SD of each group. Protein levels were compared across groups (A, C) and subgroups (B, D). (A, C) LL-37 and MPO concentrations are higher in infected (Group A and B) than in healthy urines (Control). (B, D) No difference in protein concentrations was found when comparing the subgroups of Group A. ****p < 0.0001.

    Journal: Frontiers in Immunology

    Article Title: Presence of neutrophil extracellular traps (NETs) in different types of human urinary tract infections (UTI). A pilot study

    doi: 10.3389/fimmu.2026.1745166

    Figure Lengend Snippet: Detection of cathelicidin (LL-37) and myeloperoxidase (MPO) in human urine samples. Protein concentrations in human urine samples were detected by ELISA. The samples were analyzed in a microplate reader. Bar represents mean ± SD of each group. Protein levels were compared across groups (A, C) and subgroups (B, D). (A, C) LL-37 and MPO concentrations are higher in infected (Group A and B) than in healthy urines (Control). (B, D) No difference in protein concentrations was found when comparing the subgroups of Group A. ****p < 0.0001.

    Article Snippet: For the MPO-specific ELISA kit, a 96-well high-binding polystyrene microplate (F-bottom, Greiner Bio-One, #655061) was used.

    Techniques: Enzyme-linked Immunosorbent Assay, Infection, Control