versarray 1300b liquid nitrogen cooled ccd camera system (Princeton Instruments)
90
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Princeton Instruments
versarray 1300b liquid nitrogen cooled ccd camera system
Versarray 1300b Liquid Nitrogen Cooled Ccd Camera System, supplied by Princeton Instruments, 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/cooled+ccd+camera+versarray+1300b/ccd+camera+versarray+1300b/pmc04382382-146-22-31
Average 90 stars, based on 1 article reviews
Versarray 1300b Liquid Nitrogen Cooled Ccd Camera System, supplied by Princeton Instruments, 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/cooled+ccd+camera+versarray+1300b/ccd+camera+versarray+1300b/pmc04382382-146-22-31
Average 90 stars, based on 1 article reviews
versarray 1300b liquid nitrogen cooled ccd camera system - by Bioz Stars,
2026-09
90/100 stars
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Injection:Article Title: Sustained accurate recording of intracellular acidification in living tissues with a photo-controllable bioluminescent protein Article Snippet: All images were taken using a cooled Article Title: Visualization and quantitative analysis of G protein-coupled receptor-β-arrestin interaction in single cells and specific organs of living mice using split luciferase complementation. Article Snippet: Methods used to assess the efficacy of potentially therapeutic reagents for G protein-coupled receptors (GPCRs) have been developed.. Previously, we demonstrated sensitive detection of the interaction of GPCRs and β-arrestin2 (ARRB2) using 96-well microtiter plates and a bioluminescence microscope based on split click beetle luciferase complementation.. Herein, using firefly luciferase emitting longer wavelength light, we demonstrate quantitative analysis of the interaction of β2-adrenergic receptor (ADRB2), a kind of GPCR, and ARRB2 in a 96-well plate assay with single-cell imaging. Article Title: High-Sensitivity Real-Time Imaging of Dual Protein-Protein Interactions in Living Subjects Using Multicolor Luciferases Article Snippet: Ten minutes after injection of D-luciferin, bioluminescence images were taken using a cooled Article Title: Ratiometric bioluminescence indicators for monitoring cyclic adenosine 3',5'-monophosphate in live cells based on luciferase-fragment complementation. Article Snippet: Bioluminescent indicators for cyclic 3′,5′-monophosphate AMP (cAMP) are powerful tools for noninvasive detection with high sensitivity.. However, the absolute photon counts are affected substantially by adenosine 5′-triphosphate (ATP) and D-luciferin concentrations, limiting temporal analysis in live cells.. This report describes a genetically encoded bioluminescent indicator for detecting intracellular cAMP based on complementation of split fragments of two-color luciferase mutants originated from click beetles. Transfection:Article Title: Sustained accurate recording of intracellular acidification in living tissues with a photo-controllable bioluminescent protein Article Snippet: All images were taken using a cooled Article Title: Visualization and quantitative analysis of G protein-coupled receptor-β-arrestin interaction in single cells and specific organs of living mice using split luciferase complementation. Article Snippet: Methods used to assess the efficacy of potentially therapeutic reagents for G protein-coupled receptors (GPCRs) have been developed.. Previously, we demonstrated sensitive detection of the interaction of GPCRs and β-arrestin2 (ARRB2) using 96-well microtiter plates and a bioluminescence microscope based on split click beetle luciferase complementation.. Herein, using firefly luciferase emitting longer wavelength light, we demonstrate quantitative analysis of the interaction of β2-adrenergic receptor (ADRB2), a kind of GPCR, and ARRB2 in a 96-well plate assay with single-cell imaging. Article Title: High-Sensitivity Real-Time Imaging of Dual Protein-Protein Interactions in Living Subjects Using Multicolor Luciferases Article Snippet: Ten minutes after injection of D-luciferin, bioluminescence images were taken using a cooled Article Title: Ratiometric bioluminescence indicators for monitoring cyclic adenosine 3',5'-monophosphate in live cells based on luciferase-fragment complementation. Article Snippet: Bioluminescent indicators for cyclic 3′,5′-monophosphate AMP (cAMP) are powerful tools for noninvasive detection with high sensitivity.. However, the absolute photon counts are affected substantially by adenosine 5′-triphosphate (ATP) and D-luciferin concentrations, limiting temporal analysis in live cells.. This report describes a genetically encoded bioluminescent indicator for detecting intracellular cAMP based on complementation of split fragments of two-color luciferase mutants originated from click beetles. Incubation:Article Title: Sustained accurate recording of intracellular acidification in living tissues with a photo-controllable bioluminescent protein Article Snippet: All images were taken using a cooled Article Title: Visualization and quantitative analysis of G protein-coupled receptor-β-arrestin interaction in single cells and specific organs of living mice using split luciferase complementation. Article Snippet: Methods used to assess the efficacy of potentially therapeutic reagents for G protein-coupled receptors (GPCRs) have been developed.. Previously, we demonstrated sensitive detection of the interaction of GPCRs and β-arrestin2 (ARRB2) using 96-well microtiter plates and a bioluminescence microscope based on split click beetle luciferase complementation.. Herein, using firefly luciferase emitting longer wavelength light, we demonstrate quantitative analysis of the interaction of β2-adrenergic receptor (ADRB2), a kind of GPCR, and ARRB2 in a 96-well plate assay with single-cell imaging. Article Title: High-Sensitivity Real-Time Imaging of Dual Protein-Protein Interactions in Living Subjects Using Multicolor Luciferases Article Snippet: Ten minutes after injection of D-luciferin, bioluminescence images were taken using a cooled Article Title: Ratiometric bioluminescence indicators for monitoring cyclic adenosine 3',5'-monophosphate in live cells based on luciferase-fragment complementation. Article Snippet: Bioluminescent indicators for cyclic 3′,5′-monophosphate AMP (cAMP) are powerful tools for noninvasive detection with high sensitivity.. However, the absolute photon counts are affected substantially by adenosine 5′-triphosphate (ATP) and D-luciferin concentrations, limiting temporal analysis in live cells.. This report describes a genetically encoded bioluminescent indicator for detecting intracellular cAMP based on complementation of split fragments of two-color luciferase mutants originated from click beetles. Luciferase:Article Title: Sustained accurate recording of intracellular acidification in living tissues with a photo-controllable bioluminescent protein Article Snippet: All images were taken using a cooled Article Title: Visualization and quantitative analysis of G protein-coupled receptor-β-arrestin interaction in single cells and specific organs of living mice using split luciferase complementation. Article Snippet: Methods used to assess the efficacy of potentially therapeutic reagents for G protein-coupled receptors (GPCRs) have been developed.. Previously, we demonstrated sensitive detection of the interaction of GPCRs and β-arrestin2 (ARRB2) using 96-well microtiter plates and a bioluminescence microscope based on split click beetle luciferase complementation.. Herein, using firefly luciferase emitting longer wavelength light, we demonstrate quantitative analysis of the interaction of β2-adrenergic receptor (ADRB2), a kind of GPCR, and ARRB2 in a 96-well plate assay with single-cell imaging. Article Title: High-Sensitivity Real-Time Imaging of Dual Protein-Protein Interactions in Living Subjects Using Multicolor Luciferases Article Snippet: Ten minutes after injection of D-luciferin, bioluminescence images were taken using a cooled Article Title: Ratiometric bioluminescence indicators for monitoring cyclic adenosine 3',5'-monophosphate in live cells based on luciferase-fragment complementation. Article Snippet: Bioluminescent indicators for cyclic 3′,5′-monophosphate AMP (cAMP) are powerful tools for noninvasive detection with high sensitivity.. However, the absolute photon counts are affected substantially by adenosine 5′-triphosphate (ATP) and D-luciferin concentrations, limiting temporal analysis in live cells.. This report describes a genetically encoded bioluminescent indicator for detecting intracellular cAMP based on complementation of split fragments of two-color luciferase mutants originated from click beetles. Western Blot:Article Title: Sustained accurate recording of intracellular acidification in living tissues with a photo-controllable bioluminescent protein Article Snippet: All images were taken using a cooled Article Title: Visualization and quantitative analysis of G protein-coupled receptor-β-arrestin interaction in single cells and specific organs of living mice using split luciferase complementation. Article Snippet: Methods used to assess the efficacy of potentially therapeutic reagents for G protein-coupled receptors (GPCRs) have been developed.. Previously, we demonstrated sensitive detection of the interaction of GPCRs and β-arrestin2 (ARRB2) using 96-well microtiter plates and a bioluminescence microscope based on split click beetle luciferase complementation.. Herein, using firefly luciferase emitting longer wavelength light, we demonstrate quantitative analysis of the interaction of β2-adrenergic receptor (ADRB2), a kind of GPCR, and ARRB2 in a 96-well plate assay with single-cell imaging. Article Title: High-Sensitivity Real-Time Imaging of Dual Protein-Protein Interactions in Living Subjects Using Multicolor Luciferases Article Snippet: Ten minutes after injection of D-luciferin, bioluminescence images were taken using a cooled Article Title: Ratiometric bioluminescence indicators for monitoring cyclic adenosine 3',5'-monophosphate in live cells based on luciferase-fragment complementation. Article Snippet: Bioluminescent indicators for cyclic 3′,5′-monophosphate AMP (cAMP) are powerful tools for noninvasive detection with high sensitivity.. However, the absolute photon counts are affected substantially by adenosine 5′-triphosphate (ATP) and D-luciferin concentrations, limiting temporal analysis in live cells.. This report describes a genetically encoded bioluminescent indicator for detecting intracellular cAMP based on complementation of split fragments of two-color luciferase mutants originated from click beetles. Expressing:Article Title: Sustained accurate recording of intracellular acidification in living tissues with a photo-controllable bioluminescent protein Article Snippet: All images were taken using a cooled Article Title: Visualization and quantitative analysis of G protein-coupled receptor-β-arrestin interaction in single cells and specific organs of living mice using split luciferase complementation. Article Snippet: Methods used to assess the efficacy of potentially therapeutic reagents for G protein-coupled receptors (GPCRs) have been developed.. Previously, we demonstrated sensitive detection of the interaction of GPCRs and β-arrestin2 (ARRB2) using 96-well microtiter plates and a bioluminescence microscope based on split click beetle luciferase complementation.. Herein, using firefly luciferase emitting longer wavelength light, we demonstrate quantitative analysis of the interaction of β2-adrenergic receptor (ADRB2), a kind of GPCR, and ARRB2 in a 96-well plate assay with single-cell imaging. Article Title: High-Sensitivity Real-Time Imaging of Dual Protein-Protein Interactions in Living Subjects Using Multicolor Luciferases Article Snippet: Ten minutes after injection of D-luciferin, bioluminescence images were taken using a cooled Article Title: Ratiometric bioluminescence indicators for monitoring cyclic adenosine 3',5'-monophosphate in live cells based on luciferase-fragment complementation. Article Snippet: Bioluminescent indicators for cyclic 3′,5′-monophosphate AMP (cAMP) are powerful tools for noninvasive detection with high sensitivity.. However, the absolute photon counts are affected substantially by adenosine 5′-triphosphate (ATP) and D-luciferin concentrations, limiting temporal analysis in live cells.. This report describes a genetically encoded bioluminescent indicator for detecting intracellular cAMP based on complementation of split fragments of two-color luciferase mutants originated from click beetles. Phospho-proteomics:Article Title: Sustained accurate recording of intracellular acidification in living tissues with a photo-controllable bioluminescent protein Article Snippet: All images were taken using a cooled Article Title: Visualization and quantitative analysis of G protein-coupled receptor-β-arrestin interaction in single cells and specific organs of living mice using split luciferase complementation. Article Snippet: Methods used to assess the efficacy of potentially therapeutic reagents for G protein-coupled receptors (GPCRs) have been developed.. Previously, we demonstrated sensitive detection of the interaction of GPCRs and β-arrestin2 (ARRB2) using 96-well microtiter plates and a bioluminescence microscope based on split click beetle luciferase complementation.. Herein, using firefly luciferase emitting longer wavelength light, we demonstrate quantitative analysis of the interaction of β2-adrenergic receptor (ADRB2), a kind of GPCR, and ARRB2 in a 96-well plate assay with single-cell imaging. Article Title: High-Sensitivity Real-Time Imaging of Dual Protein-Protein Interactions in Living Subjects Using Multicolor Luciferases Article Snippet: Ten minutes after injection of D-luciferin, bioluminescence images were taken using a cooled Article Title: Ratiometric bioluminescence indicators for monitoring cyclic adenosine 3',5'-monophosphate in live cells based on luciferase-fragment complementation. Article Snippet: Bioluminescent indicators for cyclic 3′,5′-monophosphate AMP (cAMP) are powerful tools for noninvasive detection with high sensitivity.. However, the absolute photon counts are affected substantially by adenosine 5′-triphosphate (ATP) and D-luciferin concentrations, limiting temporal analysis in live cells.. This report describes a genetically encoded bioluminescent indicator for detecting intracellular cAMP based on complementation of split fragments of two-color luciferase mutants originated from click beetles. Imaging:Article Title: Sustained accurate recording of intracellular acidification in living tissues with a photo-controllable bioluminescent protein Article Snippet: All images were taken using a cooled Article Title: Visualization and quantitative analysis of G protein-coupled receptor-β-arrestin interaction in single cells and specific organs of living mice using split luciferase complementation. Article Snippet: Methods used to assess the efficacy of potentially therapeutic reagents for G protein-coupled receptors (GPCRs) have been developed.. Previously, we demonstrated sensitive detection of the interaction of GPCRs and β-arrestin2 (ARRB2) using 96-well microtiter plates and a bioluminescence microscope based on split click beetle luciferase complementation.. Herein, using firefly luciferase emitting longer wavelength light, we demonstrate quantitative analysis of the interaction of β2-adrenergic receptor (ADRB2), a kind of GPCR, and ARRB2 in a 96-well plate assay with single-cell imaging. Article Title: High-Sensitivity Real-Time Imaging of Dual Protein-Protein Interactions in Living Subjects Using Multicolor Luciferases Article Snippet: Ten minutes after injection of D-luciferin, bioluminescence images were taken using a cooled Article Title: Ratiometric bioluminescence indicators for monitoring cyclic adenosine 3',5'-monophosphate in live cells based on luciferase-fragment complementation. Article Snippet: Bioluminescent indicators for cyclic 3′,5′-monophosphate AMP (cAMP) are powerful tools for noninvasive detection with high sensitivity.. However, the absolute photon counts are affected substantially by adenosine 5′-triphosphate (ATP) and D-luciferin concentrations, limiting temporal analysis in live cells.. This report describes a genetically encoded bioluminescent indicator for detecting intracellular cAMP based on complementation of split fragments of two-color luciferase mutants originated from click beetles. |