chambered glass coverslips Search Results


94
Thermo Fisher fb12566504 chambered glass coverslips ibidi cat
Fb12566504 Chambered Glass Coverslips Ibidi Cat, supplied by Thermo Fisher, 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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Corning Life Sciences glass coverslip-bottomed chambers
Glass Coverslip Bottomed Chambers, supplied by Corning Life Sciences, 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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Labtek coverslip glass 6 well chambers
Coverslip Glass 6 Well Chambers, supplied by Labtek, 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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Fisher Scientific nunctm chambered glass coverslips for live cell imaging
Nunctm Chambered Glass Coverslips For Live Cell Imaging, 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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Labtek chambered glass coverslips #1.5 labtek ii
Chambered Glass Coverslips #1.5 Labtek Ii, supplied by Labtek, 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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Fisher Scientific labtekii chamber glass coverslips
A) Structure of arylstibonic acid compounds. B) NIH3T3 cells were plated at a density of 6×104 on <t>LabTekII</t> chamber glass coverslips and were transiently transfected with GFP-VBP or GFP-Glucorticoid Receptor (GFP-GR). Cells incubated overnight with increasing concentrations of NSC13746 (0.1 μM to 100 μM), and were analyzed by FRAP on a Zeiss LSM 510 confocal microscope. For each FRAP experiment, at least 15 cells were imaged and the corrected normalized individual curves were averaged. All FRAP images presented in the paper are representative of at least 3 independent experiments in which at least 15 different cells were imaged in each experimental condition. Increasing concentrations of NSC13746 cause increased recovery of GFP-VBP while GFP-GR is not affected by the highest concentration (100 μM) of two different active drugs, NSC13746 and NSC13778. C) Cells were co-transfected with different ratios of GFP-VBP and mCherry-A-VBP and analyzed by FRAP. Increasing the amount of transfected A-ZIP (1 B-ZIP:1 A-ZIP or 1 B-ZIP:2 A-ZIP) causes faster recovery of GFP-VBP compared to the recovery of GFP-VBP alone. Increasing the amount of transfected B-ZIP (2 B-ZIP: 1 A-ZIP) does not change the recovery of GFP-VBP. GFP-GR is unaffected by co-transfection with different mCh-A-ZIPs.
Labtekii Chamber Glass Coverslips, 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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Becton Dickinson coverslips or glass chamber slides
A) Structure of arylstibonic acid compounds. B) NIH3T3 cells were plated at a density of 6×104 on <t>LabTekII</t> chamber glass coverslips and were transiently transfected with GFP-VBP or GFP-Glucorticoid Receptor (GFP-GR). Cells incubated overnight with increasing concentrations of NSC13746 (0.1 μM to 100 μM), and were analyzed by FRAP on a Zeiss LSM 510 confocal microscope. For each FRAP experiment, at least 15 cells were imaged and the corrected normalized individual curves were averaged. All FRAP images presented in the paper are representative of at least 3 independent experiments in which at least 15 different cells were imaged in each experimental condition. Increasing concentrations of NSC13746 cause increased recovery of GFP-VBP while GFP-GR is not affected by the highest concentration (100 μM) of two different active drugs, NSC13746 and NSC13778. C) Cells were co-transfected with different ratios of GFP-VBP and mCherry-A-VBP and analyzed by FRAP. Increasing the amount of transfected A-ZIP (1 B-ZIP:1 A-ZIP or 1 B-ZIP:2 A-ZIP) causes faster recovery of GFP-VBP compared to the recovery of GFP-VBP alone. Increasing the amount of transfected B-ZIP (2 B-ZIP: 1 A-ZIP) does not change the recovery of GFP-VBP. GFP-GR is unaffected by co-transfection with different mCh-A-ZIPs.
Coverslips Or Glass Chamber Slides, 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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Hausser Scientific glass coverslip hemocytometer chamber
A) Structure of arylstibonic acid compounds. B) NIH3T3 cells were plated at a density of 6×104 on <t>LabTekII</t> chamber glass coverslips and were transiently transfected with GFP-VBP or GFP-Glucorticoid Receptor (GFP-GR). Cells incubated overnight with increasing concentrations of NSC13746 (0.1 μM to 100 μM), and were analyzed by FRAP on a Zeiss LSM 510 confocal microscope. For each FRAP experiment, at least 15 cells were imaged and the corrected normalized individual curves were averaged. All FRAP images presented in the paper are representative of at least 3 independent experiments in which at least 15 different cells were imaged in each experimental condition. Increasing concentrations of NSC13746 cause increased recovery of GFP-VBP while GFP-GR is not affected by the highest concentration (100 μM) of two different active drugs, NSC13746 and NSC13778. C) Cells were co-transfected with different ratios of GFP-VBP and mCherry-A-VBP and analyzed by FRAP. Increasing the amount of transfected A-ZIP (1 B-ZIP:1 A-ZIP or 1 B-ZIP:2 A-ZIP) causes faster recovery of GFP-VBP compared to the recovery of GFP-VBP alone. Increasing the amount of transfected B-ZIP (2 B-ZIP: 1 A-ZIP) does not change the recovery of GFP-VBP. GFP-GR is unaffected by co-transfection with different mCh-A-ZIPs.
Glass Coverslip Hemocytometer Chamber, supplied by Hausser 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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LCI Corporation chamlide chambers (lci corp., seoul, korea) accommodating 18 mm-diameter coverslips or 35 mm-mattek glass bottom dishes
A) Structure of arylstibonic acid compounds. B) NIH3T3 cells were plated at a density of 6×104 on <t>LabTekII</t> chamber glass coverslips and were transiently transfected with GFP-VBP or GFP-Glucorticoid Receptor (GFP-GR). Cells incubated overnight with increasing concentrations of NSC13746 (0.1 μM to 100 μM), and were analyzed by FRAP on a Zeiss LSM 510 confocal microscope. For each FRAP experiment, at least 15 cells were imaged and the corrected normalized individual curves were averaged. All FRAP images presented in the paper are representative of at least 3 independent experiments in which at least 15 different cells were imaged in each experimental condition. Increasing concentrations of NSC13746 cause increased recovery of GFP-VBP while GFP-GR is not affected by the highest concentration (100 μM) of two different active drugs, NSC13746 and NSC13778. C) Cells were co-transfected with different ratios of GFP-VBP and mCherry-A-VBP and analyzed by FRAP. Increasing the amount of transfected A-ZIP (1 B-ZIP:1 A-ZIP or 1 B-ZIP:2 A-ZIP) causes faster recovery of GFP-VBP compared to the recovery of GFP-VBP alone. Increasing the amount of transfected B-ZIP (2 B-ZIP: 1 A-ZIP) does not change the recovery of GFP-VBP. GFP-GR is unaffected by co-transfection with different mCh-A-ZIPs.
Chamlide Chambers (Lci Corp., Seoul, Korea) Accommodating 18 Mm Diameter Coverslips Or 35 Mm Mattek Glass Bottom Dishes, supplied by LCI Corporation, 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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Ibidi USA glass bottom chambered coverslip 80287
A) Structure of arylstibonic acid compounds. B) NIH3T3 cells were plated at a density of 6×104 on <t>LabTekII</t> chamber glass coverslips and were transiently transfected with GFP-VBP or GFP-Glucorticoid Receptor (GFP-GR). Cells incubated overnight with increasing concentrations of NSC13746 (0.1 μM to 100 μM), and were analyzed by FRAP on a Zeiss LSM 510 confocal microscope. For each FRAP experiment, at least 15 cells were imaged and the corrected normalized individual curves were averaged. All FRAP images presented in the paper are representative of at least 3 independent experiments in which at least 15 different cells were imaged in each experimental condition. Increasing concentrations of NSC13746 cause increased recovery of GFP-VBP while GFP-GR is not affected by the highest concentration (100 μM) of two different active drugs, NSC13746 and NSC13778. C) Cells were co-transfected with different ratios of GFP-VBP and mCherry-A-VBP and analyzed by FRAP. Increasing the amount of transfected A-ZIP (1 B-ZIP:1 A-ZIP or 1 B-ZIP:2 A-ZIP) causes faster recovery of GFP-VBP compared to the recovery of GFP-VBP alone. Increasing the amount of transfected B-ZIP (2 B-ZIP: 1 A-ZIP) does not change the recovery of GFP-VBP. GFP-GR is unaffected by co-transfection with different mCh-A-ZIPs.
Glass Bottom Chambered Coverslip 80287, supplied by Ibidi USA, 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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Ibidi USA four-well chambered glass coverslips
A) Structure of arylstibonic acid compounds. B) NIH3T3 cells were plated at a density of 6×104 on <t>LabTekII</t> chamber glass coverslips and were transiently transfected with GFP-VBP or GFP-Glucorticoid Receptor (GFP-GR). Cells incubated overnight with increasing concentrations of NSC13746 (0.1 μM to 100 μM), and were analyzed by FRAP on a Zeiss LSM 510 confocal microscope. For each FRAP experiment, at least 15 cells were imaged and the corrected normalized individual curves were averaged. All FRAP images presented in the paper are representative of at least 3 independent experiments in which at least 15 different cells were imaged in each experimental condition. Increasing concentrations of NSC13746 cause increased recovery of GFP-VBP while GFP-GR is not affected by the highest concentration (100 μM) of two different active drugs, NSC13746 and NSC13778. C) Cells were co-transfected with different ratios of GFP-VBP and mCherry-A-VBP and analyzed by FRAP. Increasing the amount of transfected A-ZIP (1 B-ZIP:1 A-ZIP or 1 B-ZIP:2 A-ZIP) causes faster recovery of GFP-VBP compared to the recovery of GFP-VBP alone. Increasing the amount of transfected B-ZIP (2 B-ZIP: 1 A-ZIP) does not change the recovery of GFP-VBP. GFP-GR is unaffected by co-transfection with different mCh-A-ZIPs.
Four Well Chambered Glass Coverslips, supplied by Ibidi USA, 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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Matsunami Glass rectangular chamber between coverslips 60 x no. 1
A) Structure of arylstibonic acid compounds. B) NIH3T3 cells were plated at a density of 6×104 on <t>LabTekII</t> chamber glass coverslips and were transiently transfected with GFP-VBP or GFP-Glucorticoid Receptor (GFP-GR). Cells incubated overnight with increasing concentrations of NSC13746 (0.1 μM to 100 μM), and were analyzed by FRAP on a Zeiss LSM 510 confocal microscope. For each FRAP experiment, at least 15 cells were imaged and the corrected normalized individual curves were averaged. All FRAP images presented in the paper are representative of at least 3 independent experiments in which at least 15 different cells were imaged in each experimental condition. Increasing concentrations of NSC13746 cause increased recovery of GFP-VBP while GFP-GR is not affected by the highest concentration (100 μM) of two different active drugs, NSC13746 and NSC13778. C) Cells were co-transfected with different ratios of GFP-VBP and mCherry-A-VBP and analyzed by FRAP. Increasing the amount of transfected A-ZIP (1 B-ZIP:1 A-ZIP or 1 B-ZIP:2 A-ZIP) causes faster recovery of GFP-VBP compared to the recovery of GFP-VBP alone. Increasing the amount of transfected B-ZIP (2 B-ZIP: 1 A-ZIP) does not change the recovery of GFP-VBP. GFP-GR is unaffected by co-transfection with different mCh-A-ZIPs.
Rectangular Chamber Between Coverslips 60 X No. 1, supplied by Matsunami Glass, 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


A) Structure of arylstibonic acid compounds. B) NIH3T3 cells were plated at a density of 6×104 on LabTekII chamber glass coverslips and were transiently transfected with GFP-VBP or GFP-Glucorticoid Receptor (GFP-GR). Cells incubated overnight with increasing concentrations of NSC13746 (0.1 μM to 100 μM), and were analyzed by FRAP on a Zeiss LSM 510 confocal microscope. For each FRAP experiment, at least 15 cells were imaged and the corrected normalized individual curves were averaged. All FRAP images presented in the paper are representative of at least 3 independent experiments in which at least 15 different cells were imaged in each experimental condition. Increasing concentrations of NSC13746 cause increased recovery of GFP-VBP while GFP-GR is not affected by the highest concentration (100 μM) of two different active drugs, NSC13746 and NSC13778. C) Cells were co-transfected with different ratios of GFP-VBP and mCherry-A-VBP and analyzed by FRAP. Increasing the amount of transfected A-ZIP (1 B-ZIP:1 A-ZIP or 1 B-ZIP:2 A-ZIP) causes faster recovery of GFP-VBP compared to the recovery of GFP-VBP alone. Increasing the amount of transfected B-ZIP (2 B-ZIP: 1 A-ZIP) does not change the recovery of GFP-VBP. GFP-GR is unaffected by co-transfection with different mCh-A-ZIPs.

Journal: European journal of cell biology

Article Title: The arylstibonic acid compound NSC13746 disrupts B-ZIP binding to DNA in living cells

doi: 10.1016/j.ejcb.2009.11.029

Figure Lengend Snippet: A) Structure of arylstibonic acid compounds. B) NIH3T3 cells were plated at a density of 6×104 on LabTekII chamber glass coverslips and were transiently transfected with GFP-VBP or GFP-Glucorticoid Receptor (GFP-GR). Cells incubated overnight with increasing concentrations of NSC13746 (0.1 μM to 100 μM), and were analyzed by FRAP on a Zeiss LSM 510 confocal microscope. For each FRAP experiment, at least 15 cells were imaged and the corrected normalized individual curves were averaged. All FRAP images presented in the paper are representative of at least 3 independent experiments in which at least 15 different cells were imaged in each experimental condition. Increasing concentrations of NSC13746 cause increased recovery of GFP-VBP while GFP-GR is not affected by the highest concentration (100 μM) of two different active drugs, NSC13746 and NSC13778. C) Cells were co-transfected with different ratios of GFP-VBP and mCherry-A-VBP and analyzed by FRAP. Increasing the amount of transfected A-ZIP (1 B-ZIP:1 A-ZIP or 1 B-ZIP:2 A-ZIP) causes faster recovery of GFP-VBP compared to the recovery of GFP-VBP alone. Increasing the amount of transfected B-ZIP (2 B-ZIP: 1 A-ZIP) does not change the recovery of GFP-VBP. GFP-GR is unaffected by co-transfection with different mCh-A-ZIPs.

Article Snippet: Cells were plated at a density of 6 × 10 4 on LabTekII chamber glass coverslips (Nunc/Fischer Scientific, Pittsburgh, PA) and were transiently transfected with 0.5 μg DNA and 1.5 μl lipofectamine in serum-reduced OPTI-MEM media (Gibco-Invitrogen, Carlsbad, CA).

Techniques: Transfection, Incubation, Microscopy, Concentration Assay, Cotransfection