streptavidin coated clear 96 well plates Search Results


92
Revvity flashplate microplates
Flashplate Microplates, supplied by Revvity, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Revvity 384 well plate
384 Well Plate, supplied by Revvity, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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92
Revvity streptavidine coated 96 well plate
Streptavidine Coated 96 Well Plate, supplied by Revvity, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Revvity streptavidin microtitration strips 8 × 12 wells
Streptavidin Microtitration Strips 8 × 12 Wells, supplied by Revvity, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Greiner Bio streptavidin microplates
Recognition of GAG-bound mCXCL10 by h1B6 but not by h1F11 or 1A4. Experimental setups are represented schematically on the right: GAG, black curved lines; mCXCL10, red circles. A, ELISA measuring the binding of mCXCL10-heparin complexes to immobilized antibodies. Data are presented as the mean ± S.E. of triplicates and are representative of three independent experiments. B, binding of antibodies to heparan sulfate displayed mCXCL10. <t>Streptavidin</t> biosensors coated with biotinylated heparan sulfate were dipped into wells containing 100 nm mCXCL10 for 5 min. Dissociation was then recorded for 7 min before the biosensors were transferred to wells containing 1 μg/ml antibody (5 min, association). Data are representative of two independent experiments. C, mCXCL10 was coated on adherent HUVEC. Following the washes, the testing antibody, as well as the detection buffer, was added on the cells. The numbers of fluorescent events were quantified. Data are representative of two independent experiments. The white bar on the images represents 100 μm.
Streptavidin Microplates, supplied by Greiner Bio, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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streptavidin microplates - by Bioz Stars, 2026-02
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90
Fisher Scientific reacti-bind™ streptavidin coated hbc clear 384-well plates with superblock blocking buffer
Recognition of GAG-bound mCXCL10 by h1B6 but not by h1F11 or 1A4. Experimental setups are represented schematically on the right: GAG, black curved lines; mCXCL10, red circles. A, ELISA measuring the binding of mCXCL10-heparin complexes to immobilized antibodies. Data are presented as the mean ± S.E. of triplicates and are representative of three independent experiments. B, binding of antibodies to heparan sulfate displayed mCXCL10. <t>Streptavidin</t> biosensors coated with biotinylated heparan sulfate were dipped into wells containing 100 nm mCXCL10 for 5 min. Dissociation was then recorded for 7 min before the biosensors were transferred to wells containing 1 μg/ml antibody (5 min, association). Data are representative of two independent experiments. C, mCXCL10 was coated on adherent HUVEC. Following the washes, the testing antibody, as well as the detection buffer, was added on the cells. The numbers of fluorescent events were quantified. Data are representative of two independent experiments. The white bar on the images represents 100 μm.
Reacti Bind™ Streptavidin Coated Hbc Clear 384 Well Plates With Superblock Blocking Buffer, supplied by Fisher Scientific, 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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Average 90 stars, based on 1 article reviews
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90
Greiner Bio streptavidin coated greiner microtiter plate
Recognition of GAG-bound mCXCL10 by h1B6 but not by h1F11 or 1A4. Experimental setups are represented schematically on the right: GAG, black curved lines; mCXCL10, red circles. A, ELISA measuring the binding of mCXCL10-heparin complexes to immobilized antibodies. Data are presented as the mean ± S.E. of triplicates and are representative of three independent experiments. B, binding of antibodies to heparan sulfate displayed mCXCL10. <t>Streptavidin</t> biosensors coated with biotinylated heparan sulfate were dipped into wells containing 100 nm mCXCL10 for 5 min. Dissociation was then recorded for 7 min before the biosensors were transferred to wells containing 1 μg/ml antibody (5 min, association). Data are representative of two independent experiments. C, mCXCL10 was coated on adherent HUVEC. Following the washes, the testing antibody, as well as the detection buffer, was added on the cells. The numbers of fluorescent events were quantified. Data are representative of two independent experiments. The white bar on the images represents 100 μm.
Streptavidin Coated Greiner Microtiter Plate, supplied by Greiner Bio, 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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90
Thomas Scientific nunc streptavidin-coated 96-well plates
Recognition of GAG-bound mCXCL10 by h1B6 but not by h1F11 or 1A4. Experimental setups are represented schematically on the right: GAG, black curved lines; mCXCL10, red circles. A, ELISA measuring the binding of mCXCL10-heparin complexes to immobilized antibodies. Data are presented as the mean ± S.E. of triplicates and are representative of three independent experiments. B, binding of antibodies to heparan sulfate displayed mCXCL10. <t>Streptavidin</t> biosensors coated with biotinylated heparan sulfate were dipped into wells containing 100 nm mCXCL10 for 5 min. Dissociation was then recorded for 7 min before the biosensors were transferred to wells containing 1 μg/ml antibody (5 min, association). Data are representative of two independent experiments. C, mCXCL10 was coated on adherent HUVEC. Following the washes, the testing antibody, as well as the detection buffer, was added on the cells. The numbers of fluorescent events were quantified. Data are representative of two independent experiments. The white bar on the images represents 100 μm.
Nunc Streptavidin Coated 96 Well Plates, supplied by Thomas Scientific, 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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Meso Scale Diagnostics LLC streptavidin-coated 96-well ecl plates
Recognition of GAG-bound mCXCL10 by h1B6 but not by h1F11 or 1A4. Experimental setups are represented schematically on the right: GAG, black curved lines; mCXCL10, red circles. A, ELISA measuring the binding of mCXCL10-heparin complexes to immobilized antibodies. Data are presented as the mean ± S.E. of triplicates and are representative of three independent experiments. B, binding of antibodies to heparan sulfate displayed mCXCL10. <t>Streptavidin</t> biosensors coated with biotinylated heparan sulfate were dipped into wells containing 100 nm mCXCL10 for 5 min. Dissociation was then recorded for 7 min before the biosensors were transferred to wells containing 1 μg/ml antibody (5 min, association). Data are representative of two independent experiments. C, mCXCL10 was coated on adherent HUVEC. Following the washes, the testing antibody, as well as the detection buffer, was added on the cells. The numbers of fluorescent events were quantified. Data are representative of two independent experiments. The white bar on the images represents 100 μm.
Streptavidin Coated 96 Well Ecl Plates, supplied by Meso Scale Diagnostics LLC, 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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90
Fisher Scientific delphia 200 ll streptavidin clear coated 96-well plates
Recognition of GAG-bound mCXCL10 by h1B6 but not by h1F11 or 1A4. Experimental setups are represented schematically on the right: GAG, black curved lines; mCXCL10, red circles. A, ELISA measuring the binding of mCXCL10-heparin complexes to immobilized antibodies. Data are presented as the mean ± S.E. of triplicates and are representative of three independent experiments. B, binding of antibodies to heparan sulfate displayed mCXCL10. <t>Streptavidin</t> biosensors coated with biotinylated heparan sulfate were dipped into wells containing 100 nm mCXCL10 for 5 min. Dissociation was then recorded for 7 min before the biosensors were transferred to wells containing 1 μg/ml antibody (5 min, association). Data are representative of two independent experiments. C, mCXCL10 was coated on adherent HUVEC. Following the washes, the testing antibody, as well as the detection buffer, was added on the cells. The numbers of fluorescent events were quantified. Data are representative of two independent experiments. The white bar on the images represents 100 μm.
Delphia 200 Ll Streptavidin Clear Coated 96 Well Plates, supplied by Fisher Scientific, 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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90
Becton Dickinson streptavidin-coated 96-well plates
Recognition of GAG-bound mCXCL10 by h1B6 but not by h1F11 or 1A4. Experimental setups are represented schematically on the right: GAG, black curved lines; mCXCL10, red circles. A, ELISA measuring the binding of mCXCL10-heparin complexes to immobilized antibodies. Data are presented as the mean ± S.E. of triplicates and are representative of three independent experiments. B, binding of antibodies to heparan sulfate displayed mCXCL10. <t>Streptavidin</t> biosensors coated with biotinylated heparan sulfate were dipped into wells containing 100 nm mCXCL10 for 5 min. Dissociation was then recorded for 7 min before the biosensors were transferred to wells containing 1 μg/ml antibody (5 min, association). Data are representative of two independent experiments. C, mCXCL10 was coated on adherent HUVEC. Following the washes, the testing antibody, as well as the detection buffer, was added on the cells. The numbers of fluorescent events were quantified. Data are representative of two independent experiments. The white bar on the images represents 100 μm.
Streptavidin Coated 96 Well Plates, supplied by Becton Dickinson, 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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MicroCoat Biotechnologie 384 well streptavidin coated microtiter plates
Recognition of GAG-bound mCXCL10 by h1B6 but not by h1F11 or 1A4. Experimental setups are represented schematically on the right: GAG, black curved lines; mCXCL10, red circles. A, ELISA measuring the binding of mCXCL10-heparin complexes to immobilized antibodies. Data are presented as the mean ± S.E. of triplicates and are representative of three independent experiments. B, binding of antibodies to heparan sulfate displayed mCXCL10. <t>Streptavidin</t> biosensors coated with biotinylated heparan sulfate were dipped into wells containing 100 nm mCXCL10 for 5 min. Dissociation was then recorded for 7 min before the biosensors were transferred to wells containing 1 μg/ml antibody (5 min, association). Data are representative of two independent experiments. C, mCXCL10 was coated on adherent HUVEC. Following the washes, the testing antibody, as well as the detection buffer, was added on the cells. The numbers of fluorescent events were quantified. Data are representative of two independent experiments. The white bar on the images represents 100 μm.
384 Well Streptavidin Coated Microtiter Plates, supplied by MicroCoat Biotechnologie, 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


Recognition of GAG-bound mCXCL10 by h1B6 but not by h1F11 or 1A4. Experimental setups are represented schematically on the right: GAG, black curved lines; mCXCL10, red circles. A, ELISA measuring the binding of mCXCL10-heparin complexes to immobilized antibodies. Data are presented as the mean ± S.E. of triplicates and are representative of three independent experiments. B, binding of antibodies to heparan sulfate displayed mCXCL10. Streptavidin biosensors coated with biotinylated heparan sulfate were dipped into wells containing 100 nm mCXCL10 for 5 min. Dissociation was then recorded for 7 min before the biosensors were transferred to wells containing 1 μg/ml antibody (5 min, association). Data are representative of two independent experiments. C, mCXCL10 was coated on adherent HUVEC. Following the washes, the testing antibody, as well as the detection buffer, was added on the cells. The numbers of fluorescent events were quantified. Data are representative of two independent experiments. The white bar on the images represents 100 μm.

Journal: The Journal of Biological Chemistry

Article Title: Antibody Neutralization of CXCL10 in Vivo Is Dependent on Binding to Free and Not Endothelial-bound Chemokine

doi: 10.1074/jbc.M116.745877

Figure Lengend Snippet: Recognition of GAG-bound mCXCL10 by h1B6 but not by h1F11 or 1A4. Experimental setups are represented schematically on the right: GAG, black curved lines; mCXCL10, red circles. A, ELISA measuring the binding of mCXCL10-heparin complexes to immobilized antibodies. Data are presented as the mean ± S.E. of triplicates and are representative of three independent experiments. B, binding of antibodies to heparan sulfate displayed mCXCL10. Streptavidin biosensors coated with biotinylated heparan sulfate were dipped into wells containing 100 nm mCXCL10 for 5 min. Dissociation was then recorded for 7 min before the biosensors were transferred to wells containing 1 μg/ml antibody (5 min, association). Data are representative of two independent experiments. C, mCXCL10 was coated on adherent HUVEC. Following the washes, the testing antibody, as well as the detection buffer, was added on the cells. The numbers of fluorescent events were quantified. Data are representative of two independent experiments. The white bar on the images represents 100 μm.

Article Snippet: Plasma samples were added on biotinylated mCXCL10 (Almac, Craigavon, United Kingdom) captured beforehand on streptavidin microplates (Greiner Bio-One).

Techniques: Enzyme-linked Immunosorbent Assay, Binding Assay

Inhibition of mCXCL10 binding to GAGs by h1F11. A, immobilized antibodies were incubated with 50 nm mCXCL10. FITC-tagged heparin was then added on the antibody-chemokine complexes, and bound heparin was detected with an anti-FITC. Data are presented as the mean ± S.E. of duplicates and are representative of two independent experiments. B, biolayer interferometry. Streptavidin biosensors were loaded with biotinylated heparan sulfate and dipped into a solution containing a constant concentration of 30 nm chemokine and a dose response of h1F11; these were preincubated to allow complex formation. A clear decrease in signal was observed with increasing concentrations of h1F11 (top graph). The dose-dependent inhibition of the maximal response is shown on the bottom graph.

Journal: The Journal of Biological Chemistry

Article Title: Antibody Neutralization of CXCL10 in Vivo Is Dependent on Binding to Free and Not Endothelial-bound Chemokine

doi: 10.1074/jbc.M116.745877

Figure Lengend Snippet: Inhibition of mCXCL10 binding to GAGs by h1F11. A, immobilized antibodies were incubated with 50 nm mCXCL10. FITC-tagged heparin was then added on the antibody-chemokine complexes, and bound heparin was detected with an anti-FITC. Data are presented as the mean ± S.E. of duplicates and are representative of two independent experiments. B, biolayer interferometry. Streptavidin biosensors were loaded with biotinylated heparan sulfate and dipped into a solution containing a constant concentration of 30 nm chemokine and a dose response of h1F11; these were preincubated to allow complex formation. A clear decrease in signal was observed with increasing concentrations of h1F11 (top graph). The dose-dependent inhibition of the maximal response is shown on the bottom graph.

Article Snippet: Plasma samples were added on biotinylated mCXCL10 (Almac, Craigavon, United Kingdom) captured beforehand on streptavidin microplates (Greiner Bio-One).

Techniques: Inhibition, Binding Assay, Incubation, Concentration Assay