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Evident Corporation fluoview 1000 software package
Fluoview 1000 Software Package, supplied by Evident Corporation, 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/fluoview+1000+software/bx51+microscope/pm39188056-125-1-5
Average 90 stars, based on 1 article reviews
fluoview 1000 software package - by Bioz Stars, 2026-09
90/100 stars

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Related Articles

Software:

Article Title: A Novel Role for Wnt/Ca 2+ Signaling in Actin Cytoskeleton Remodeling and Cell Motility in Prostate Cancer
Article Snippet: .. Image and data acquisition was performed using FluoView 1000 software (Olympus). .. Fluorescent intensity was measured and data exported as a tab delimited file for further analysis using Image J and Origin (Microcal) software.

Article Title: Regulation of cadherin expression in the chicken neural crest by the Wnt/?-catenin signaling pathway
Article Snippet: .. The intensity measurement tool of Olympus Fluoview 1000 software was used for measuring the intensity of fluorescence for cadherin-7 and cadherin-11 immunostained proteins. ..

Article Title: Identification and validation of Rab11a in Rat orofacial inflammatory pain model induced by CFA.
Article Snippet: Orofacial pain (OFP) is a clinically very common and the most troubling condition; however, there is few effective way to relieve OFP.. Rab11a, a small molecule guanosine triphosphate enzyme, is one of the Rab member family playing a vital role in intracellular endocytosis and the pain process.. Therefore, we investigated the hub genes of rat OFP model induced by Complete Freund’s Adjuvant (CFA) via re-analyzing microarray data (GSE111160).

Article Title: Identification of a novel mitochondria-localized LKB1 variant required for the regulation of the oxidative stress response.
Article Snippet: Immunofluorescence images were captured using Olympus Fluoview 1000 confocal microscope. .. Image analyses and measurements were performed using Olympus Fluoview 1000 software and ImageJ. ..

Article Title: Spatio-Temporal Expression and Functional Involvement of Transient Receptor Potential Vanilloid 1 in Diabetic Mechanical Allodynia in Rats
Article Snippet: .. Images were observed by a confocal laser scanning microscope (FV1000, Olympus, Tokyo, Japan) and digital images were captured with the Fluoview 1000 software (Olympus). ..

Article Title: RAL-1 signaling regulates lipid composition in C. elegans
Article Snippet: Briefly, an Olympus IX81 inverted laser-scanning confocal microscope optimized for near infrared signal detected signal generated by temporally overlapping Pump and Stokes laser beams and optimized for lipids contained in lipid droplets . .. Images were processed using Olympus Fluoview 1000 software. ..

Article Title: Drosophila pVALIUM10 TRiP RNAi lines cause undesired silencing of Gateway-based transgenes
Article Snippet: Confocal images and stacks were acquired with an Olympus FV1000 confocal microscope equipped with 20× UPlan S-Apo (NA 0.85), 40× UPlan FL (NA 1.30), and 60× UPlanApo (NA 1.35) objectives. .. Maximum Z-projections were generated from consecutive sections taken at 1.4- μ m steps using the FluoView 1000 software (Olympus) (RRID: SCR_014215) and Fiji ( https://fiji.sc/ ) (RRID:SCR_002285). ..

Article Title: Neuroprotective actions of a fatty acid nitroalkene in Parkinson’s disease
Article Snippet: .. Fluorescent images were taken using an Olympus BX61 confocal microscope and Fluoview 1000 software (Melville, NY). ..

Fluorescence:

Article Title: Regulation of cadherin expression in the chicken neural crest by the Wnt/?-catenin signaling pathway
Article Snippet: .. The intensity measurement tool of Olympus Fluoview 1000 software was used for measuring the intensity of fluorescence for cadherin-7 and cadherin-11 immunostained proteins. ..

Laser-Scanning Microscopy:

Article Title: Spatio-Temporal Expression and Functional Involvement of Transient Receptor Potential Vanilloid 1 in Diabetic Mechanical Allodynia in Rats
Article Snippet: .. Images were observed by a confocal laser scanning microscope (FV1000, Olympus, Tokyo, Japan) and digital images were captured with the Fluoview 1000 software (Olympus). ..

Generated:

Article Title: Drosophila pVALIUM10 TRiP RNAi lines cause undesired silencing of Gateway-based transgenes
Article Snippet: Confocal images and stacks were acquired with an Olympus FV1000 confocal microscope equipped with 20× UPlan S-Apo (NA 0.85), 40× UPlan FL (NA 1.30), and 60× UPlanApo (NA 1.35) objectives. .. Maximum Z-projections were generated from consecutive sections taken at 1.4- μ m steps using the FluoView 1000 software (Olympus) (RRID: SCR_014215) and Fiji ( https://fiji.sc/ ) (RRID:SCR_002285). ..

Microscopy:

Article Title: Neuroprotective actions of a fatty acid nitroalkene in Parkinson’s disease
Article Snippet: .. Fluorescent images were taken using an Olympus BX61 confocal microscope and Fluoview 1000 software (Melville, NY). ..



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Evident Corporation fluoview 1000 software (fv1000
The ME-MPM design . ( a ) Optical setup for multiple-excitation multiphoton microscopy (ME-MPM) measurements. Beams from Mai Tai broad-band (BB) and Mai Tai high power (HP) sources were directed to either an upright confocal microscope (FV300) or an inverted confocal microscope <t>(FV1000).</t> Note that the Nicol prisms split the beam into two paths directed to either microscope for both lasers. The setting of each polarizer can be easily adjusted by rotating the preceding half-wave plate to direct more or less light toward each system, allowing for optimal excitation of each fluorophore during dual color imaging. The control of half-wave plates i, ii, and iii is described in the text and in Additional file . ( b ) Two-photon absorption (TPA) spectra for EGFP and DsRedII fluorescent proteins in Goeppert-Mayer units. ( c ) TPA spectra for the hydrazine derivatives of FITC (green), and Alexa Fluor 594 (red) in Goeppert-Mayer units. We do not present the spectra in terms of TPA brightness, σ 2 × φ , where φ is the fluorescence quantum yield, because the quantum yields of these dyes are similar in the same environment and they are quite sensitive to pH and other conditions . Imaging experiments presented here were performed at 920 nm for green-emitting fluorophores and at 1015 to 1040 nm for red-emitting fluorophores.
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fluoview 1000 software (fv1000 - by Bioz Stars, 2026-09
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  Buy from Supplier

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The ME-MPM design . ( a ) Optical setup for multiple-excitation multiphoton microscopy (ME-MPM) measurements. Beams from Mai Tai broad-band (BB) and Mai Tai high power (HP) sources were directed to either an upright confocal microscope (FV300) or an inverted confocal microscope (FV1000). Note that the Nicol prisms split the beam into two paths directed to either microscope for both lasers. The setting of each polarizer can be easily adjusted by rotating the preceding half-wave plate to direct more or less light toward each system, allowing for optimal excitation of each fluorophore during dual color imaging. The control of half-wave plates i, ii, and iii is described in the text and in Additional file . ( b ) Two-photon absorption (TPA) spectra for EGFP and DsRedII fluorescent proteins in Goeppert-Mayer units. ( c ) TPA spectra for the hydrazine derivatives of FITC (green), and Alexa Fluor 594 (red) in Goeppert-Mayer units. We do not present the spectra in terms of TPA brightness, σ 2 × φ , where φ is the fluorescence quantum yield, because the quantum yields of these dyes are similar in the same environment and they are quite sensitive to pH and other conditions . Imaging experiments presented here were performed at 920 nm for green-emitting fluorophores and at 1015 to 1040 nm for red-emitting fluorophores.

Journal: BMC Biotechnology

Article Title: Simultaneous multiple-excitation multiphoton microscopy yields increased imaging sensitivity and specificity

doi: 10.1186/1472-6750-11-20

Figure Lengend Snippet: The ME-MPM design . ( a ) Optical setup for multiple-excitation multiphoton microscopy (ME-MPM) measurements. Beams from Mai Tai broad-band (BB) and Mai Tai high power (HP) sources were directed to either an upright confocal microscope (FV300) or an inverted confocal microscope (FV1000). Note that the Nicol prisms split the beam into two paths directed to either microscope for both lasers. The setting of each polarizer can be easily adjusted by rotating the preceding half-wave plate to direct more or less light toward each system, allowing for optimal excitation of each fluorophore during dual color imaging. The control of half-wave plates i, ii, and iii is described in the text and in Additional file . ( b ) Two-photon absorption (TPA) spectra for EGFP and DsRedII fluorescent proteins in Goeppert-Mayer units. ( c ) TPA spectra for the hydrazine derivatives of FITC (green), and Alexa Fluor 594 (red) in Goeppert-Mayer units. We do not present the spectra in terms of TPA brightness, σ 2 × φ , where φ is the fluorescence quantum yield, because the quantum yields of these dyes are similar in the same environment and they are quite sensitive to pH and other conditions . Imaging experiments presented here were performed at 920 nm for green-emitting fluorophores and at 1015 to 1040 nm for red-emitting fluorophores.

Article Snippet: ME-MPM was conducted on an upright Olympus confocal point scanning system equipped with FluoView 300 software (FV300) or an inverted Olympus spectral deconvolution confocal point scanning system equipped with variable band-pass filters (VBFs) and FluoView 1000 software (FV1000) using Spectra Physics Mai Tai broad-band (BB, 710 nm - 990 nm) and Mai Tai high-power (HP, 690 nm - 1040 nm) two-photon excitation sources (Figure ).

Techniques: Microscopy, Imaging, Fluorescence