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Compix Inc simple pci image capture software
Simple Pci Image Capture Software, supplied by Compix Inc, 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/simple+pci+imaging+software/simple+pci+imaging+software/pmc02730818-185-81-86
Average 90 stars, based on 1 article reviews
simple pci image capture software - by Bioz Stars, 2026-11
90/100 stars

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Related Articles

Imaging:

Article Title: Self-Assembly of Macromolecules Within Single Topological Defects of Nematic Solvents
Article Snippet: Solvent-mediated self-assembly of macromolecules has been widely used as a bottom-up strategy for synthesis of nanostructured materials, but most solvents (e.g., water or isotropic organic solvents) provide limited control over the spatial localization and manipulation of individual assemblies.. In this study, we use organic solvents with nematic ordering to explore the possibility of programmed assembly of polymers with tailored side-chains within the nanoscopic cores of topological defects of the nematic solvents by developing structure-property relationships.. Variation of the side chains of poly(n-alkyl acrylates) (alkyl = butyl, hexyl, and dodecyl) revealed that the driving force for partitioning of the polymers into the nanoscopic cores of topological defects formed in nematic 4’-n-pentyl-4-biphenylcarbonitrile (5CB) increased with sidechain length, but controlled self-assembly was not observed.

Article Title: Tauroursodeoxycholic acid acts via TGR5 receptor to facilitate DNA damage repair and improve early porcine embryo development.
Article Snippet: Funding information Natural Sciences and Engineering Research Council of Canada, Grant/Award Numbers: RGPIN‐2015‐04390, RGPIN‐2016‐04910; Quebec Research Fund – Nature and Technology (FQRNT) Doctoral Scholarship; NSERC Alexander Graham Bell Canada Graduate Scholarship; Scholarships from the Coordination for the Improvement of Higher Education Personnel (CAPES) Abstract DNA damage associated with assisted reproductive technologies is an important factor affecting gamete fertility and embryo development.. Activation of the TGR5 receptor by tauroursodeoxycholic acid (TUDCA) has been shown to reduce endoplasmic reticulum (ER) stress in embryos; however, its effect on genome damage responses (GDR) activation to facilitate DNA damage repair has not been examined.. This study aimed to investigate the effect of TUDCA on DNA damage repair and embryo development.

Article Title: Using Long-term Time-lapse Imaging of Mammalian Cell Cycle Progression for Laboratory Instruction and Analysis
Article Snippet: .. The time-lapse images were generated using Simple PCI imaging software (Compix, Brandywine, PA). .. Time-lapse image sequences were converted from the Compix cxd file format to audio-video interleave (AVI) movies.

Article Title: Select Septate Junction Proteins Direct ROS-Mediated Paracrine Regulation of Drosophila Cardiac Function
Article Snippet: High-speed 30 s movies were recorded at a rate of > 150 frames per second using a Hamamatsu CCD camera on a Nikon 80i upright microscope with a 10x dipping immersion lens. .. The images were processed using Simple PCI imaging software (Compix Inc.). .. M-modes and quantitative data were generated using a MATLAB-based image analysis program ( Fink et al., 2009 ).

Article Title: Supplementation of oleic acid, stearic acid, palmitic acid and β-hydroxybutyrate increase H3K9me3 in endometrial epithelial cells of cattle cultured in vitro.
Article Snippet: There is growing evidence that greater than homeostatic blood concentrations of nonesterified fatty acids (NEFAs) and β-hydroxybutyrate (BHBA) have negative consequences on dairy cow’s fertility, but effects on cell homeostasis in the reproductive system is not completely understood.. In this study, lipids accumulation, reactive oxygen species (ROS) concentrations, abundance of gene transcripts, and immunofluorescence signal of H3K4me3 and H3K9me3 were evaluated in endometrial epithelial cells of cattle cultured with NEFAs (Oleic (OA), Stearic (SA) and Palmitic (PA) acids), BHBA, NEFAs + BHBA or each of the three NEFAs alone.. The cellular lipids were in greater concentrations as a result of NEFAs + BHBA, NEFAs, SA or OA supplementation, but not by BHBA or PA.

Article Title: The activation of cardiac dSir2 -related pathways mediates physical exercise resistance to heart aging in old Drosophila
Article Snippet: .. All images were acquired and contrast enhanced using Simple PCI imaging software (Compix, Sewickley, PA). ..

Article Title: Cardiac Snail family of transcription factors directs systemic lipid metabolism in Drosophila.
Article Snippet: High-speed 30-s movies were recorded at a rate of>150 frames per second using a Hamamatsu CCD camera on a Nikon 80i upright microscope with a 10x dipping immersion lens. .. The images were processed using Simple PCI imaging software (Compix Inc.). .. Quantitative data were generated using a MatLab-based image analysis program.

Software:

Article Title: Self-Assembly of Macromolecules Within Single Topological Defects of Nematic Solvents
Article Snippet: Solvent-mediated self-assembly of macromolecules has been widely used as a bottom-up strategy for synthesis of nanostructured materials, but most solvents (e.g., water or isotropic organic solvents) provide limited control over the spatial localization and manipulation of individual assemblies.. In this study, we use organic solvents with nematic ordering to explore the possibility of programmed assembly of polymers with tailored side-chains within the nanoscopic cores of topological defects of the nematic solvents by developing structure-property relationships.. Variation of the side chains of poly(n-alkyl acrylates) (alkyl = butyl, hexyl, and dodecyl) revealed that the driving force for partitioning of the polymers into the nanoscopic cores of topological defects formed in nematic 4’-n-pentyl-4-biphenylcarbonitrile (5CB) increased with sidechain length, but controlled self-assembly was not observed.

Article Title: Tauroursodeoxycholic acid acts via TGR5 receptor to facilitate DNA damage repair and improve early porcine embryo development.
Article Snippet: Funding information Natural Sciences and Engineering Research Council of Canada, Grant/Award Numbers: RGPIN‐2015‐04390, RGPIN‐2016‐04910; Quebec Research Fund – Nature and Technology (FQRNT) Doctoral Scholarship; NSERC Alexander Graham Bell Canada Graduate Scholarship; Scholarships from the Coordination for the Improvement of Higher Education Personnel (CAPES) Abstract DNA damage associated with assisted reproductive technologies is an important factor affecting gamete fertility and embryo development.. Activation of the TGR5 receptor by tauroursodeoxycholic acid (TUDCA) has been shown to reduce endoplasmic reticulum (ER) stress in embryos; however, its effect on genome damage responses (GDR) activation to facilitate DNA damage repair has not been examined.. This study aimed to investigate the effect of TUDCA on DNA damage repair and embryo development.

Article Title: Using Long-term Time-lapse Imaging of Mammalian Cell Cycle Progression for Laboratory Instruction and Analysis
Article Snippet: .. The time-lapse images were generated using Simple PCI imaging software (Compix, Brandywine, PA). .. Time-lapse image sequences were converted from the Compix cxd file format to audio-video interleave (AVI) movies.

Article Title: Select Septate Junction Proteins Direct ROS-Mediated Paracrine Regulation of Drosophila Cardiac Function
Article Snippet: High-speed 30 s movies were recorded at a rate of > 150 frames per second using a Hamamatsu CCD camera on a Nikon 80i upright microscope with a 10x dipping immersion lens. .. The images were processed using Simple PCI imaging software (Compix Inc.). .. M-modes and quantitative data were generated using a MATLAB-based image analysis program ( Fink et al., 2009 ).

Article Title: Supplementation of oleic acid, stearic acid, palmitic acid and β-hydroxybutyrate increase H3K9me3 in endometrial epithelial cells of cattle cultured in vitro.
Article Snippet: There is growing evidence that greater than homeostatic blood concentrations of nonesterified fatty acids (NEFAs) and β-hydroxybutyrate (BHBA) have negative consequences on dairy cow’s fertility, but effects on cell homeostasis in the reproductive system is not completely understood.. In this study, lipids accumulation, reactive oxygen species (ROS) concentrations, abundance of gene transcripts, and immunofluorescence signal of H3K4me3 and H3K9me3 were evaluated in endometrial epithelial cells of cattle cultured with NEFAs (Oleic (OA), Stearic (SA) and Palmitic (PA) acids), BHBA, NEFAs + BHBA or each of the three NEFAs alone.. The cellular lipids were in greater concentrations as a result of NEFAs + BHBA, NEFAs, SA or OA supplementation, but not by BHBA or PA.

Article Title: The activation of cardiac dSir2 -related pathways mediates physical exercise resistance to heart aging in old Drosophila
Article Snippet: .. All images were acquired and contrast enhanced using Simple PCI imaging software (Compix, Sewickley, PA). ..

Article Title: Cardiac Snail family of transcription factors directs systemic lipid metabolism in Drosophila.
Article Snippet: High-speed 30-s movies were recorded at a rate of>150 frames per second using a Hamamatsu CCD camera on a Nikon 80i upright microscope with a 10x dipping immersion lens. .. The images were processed using Simple PCI imaging software (Compix Inc.). .. Quantitative data were generated using a MatLab-based image analysis program.

Microscopy:

Article Title: Tauroursodeoxycholic acid acts via TGR5 receptor to facilitate DNA damage repair and improve early porcine embryo development.
Article Snippet: Funding information Natural Sciences and Engineering Research Council of Canada, Grant/Award Numbers: RGPIN‐2015‐04390, RGPIN‐2016‐04910; Quebec Research Fund – Nature and Technology (FQRNT) Doctoral Scholarship; NSERC Alexander Graham Bell Canada Graduate Scholarship; Scholarships from the Coordination for the Improvement of Higher Education Personnel (CAPES) Abstract DNA damage associated with assisted reproductive technologies is an important factor affecting gamete fertility and embryo development.. Activation of the TGR5 receptor by tauroursodeoxycholic acid (TUDCA) has been shown to reduce endoplasmic reticulum (ER) stress in embryos; however, its effect on genome damage responses (GDR) activation to facilitate DNA damage repair has not been examined.. This study aimed to investigate the effect of TUDCA on DNA damage repair and embryo development.

Generated:

Article Title: Using Long-term Time-lapse Imaging of Mammalian Cell Cycle Progression for Laboratory Instruction and Analysis
Article Snippet: .. The time-lapse images were generated using Simple PCI imaging software (Compix, Brandywine, PA). .. Time-lapse image sequences were converted from the Compix cxd file format to audio-video interleave (AVI) movies.

Fluorescence:

Article Title: Supplementation of oleic acid, stearic acid, palmitic acid and β-hydroxybutyrate increase H3K9me3 in endometrial epithelial cells of cattle cultured in vitro.
Article Snippet: There is growing evidence that greater than homeostatic blood concentrations of nonesterified fatty acids (NEFAs) and β-hydroxybutyrate (BHBA) have negative consequences on dairy cow’s fertility, but effects on cell homeostasis in the reproductive system is not completely understood.. In this study, lipids accumulation, reactive oxygen species (ROS) concentrations, abundance of gene transcripts, and immunofluorescence signal of H3K4me3 and H3K9me3 were evaluated in endometrial epithelial cells of cattle cultured with NEFAs (Oleic (OA), Stearic (SA) and Palmitic (PA) acids), BHBA, NEFAs + BHBA or each of the three NEFAs alone.. The cellular lipids were in greater concentrations as a result of NEFAs + BHBA, NEFAs, SA or OA supplementation, but not by BHBA or PA.



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Trophoblast invasion from first-trimester chorionic villous explants. First-trimester villous explants were cultured on Matrigel-coated transwell inserts and treated with vehicle or 350 ng/mL sildenafil for 72 hours before fixation. Examples of outgrowths from villous explants cultured with vehicle (A, C, E) or 350 ng/mL sildenafil (B, E, F) are shown. Bright-field images (A, B) and paired fields labeled with 6-diamino-2-phenylindole (C, D) or anti-Ki67 (E, F) are included. Size bar in (A) applies to all image panels. Outgrowth length and cell proliferation were measured using Simple <t>PCI</t> image <t>analysis</t> <t>software</t> (G, H). The graph in (G) shows outgrowth lengths for triplicate experiments in which 10 villous explants were measured for each treatment. * P<.05 vs. vehicle. The graph in (H) shows the percentage of cell nuclei in the outgrowth regions that were labeled with anti-Ki67 antibody. The differences between vehicle- and sildenafil-treated explants were not significant (n = 8). Error bars represent SEM.
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Trophoblast invasion from first-trimester chorionic villous explants. First-trimester villous explants were cultured on Matrigel-coated transwell inserts and treated with vehicle or 350 ng/mL sildenafil for 72 hours before fixation. Examples of outgrowths from villous explants cultured with vehicle (A, C, E) or 350 ng/mL sildenafil (B, E, F) are shown. Bright-field images (A, B) and paired fields labeled with 6-diamino-2-phenylindole (C, D) or anti-Ki67 (E, F) are included. Size bar in (A) applies to all image panels. Outgrowth length and cell proliferation were measured using Simple <t>PCI</t> image <t>analysis</t> <t>software</t> (G, H). The graph in (G) shows outgrowth lengths for triplicate experiments in which 10 villous explants were measured for each treatment. * P<.05 vs. vehicle. The graph in (H) shows the percentage of cell nuclei in the outgrowth regions that were labeled with anti-Ki67 antibody. The differences between vehicle- and sildenafil-treated explants were not significant (n = 8). Error bars represent SEM.
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Trophoblast invasion from first-trimester chorionic villous explants. First-trimester villous explants were cultured on Matrigel-coated transwell inserts and treated with vehicle or 350 ng/mL sildenafil for 72 hours before fixation. Examples of outgrowths from villous explants cultured with vehicle (A, C, E) or 350 ng/mL sildenafil (B, E, F) are shown. Bright-field images (A, B) and paired fields labeled with 6-diamino-2-phenylindole (C, D) or anti-Ki67 (E, F) are included. Size bar in (A) applies to all image panels. Outgrowth length and cell proliferation were measured using Simple <t>PCI</t> image <t>analysis</t> <t>software</t> (G, H). The graph in (G) shows outgrowth lengths for triplicate experiments in which 10 villous explants were measured for each treatment. * P<.05 vs. vehicle. The graph in (H) shows the percentage of cell nuclei in the outgrowth regions that were labeled with anti-Ki67 antibody. The differences between vehicle- and sildenafil-treated explants were not significant (n = 8). Error bars represent SEM.
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Semiquantitative assessment and localization of CBS and CSE. UA sections were labeled with antibodies against CBS, or CSE (not shown), followed by secondary Alexa488 (green)-labeled secondary antibody. Endothelial cells were labeled with CD31 followed by Alexa568 (red)-labeled secondary antibody. Cell nuclei were stained with DAPI. Negative control treated with IgG or with primary antibody omitted is shown in first panel. Representative outline of border between UA intima and media was indicated, and UA lumen (l), intima (i), and media (m) were denoted (second panel). Regions of interest for intima (ROI – i) and media (ROI – m) used for analysis in Simple <t>PCI</t> <t>software</t> are illustrated (third panel). Scale bar is 25 μm
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Image Search Results


Trophoblast invasion from first-trimester chorionic villous explants. First-trimester villous explants were cultured on Matrigel-coated transwell inserts and treated with vehicle or 350 ng/mL sildenafil for 72 hours before fixation. Examples of outgrowths from villous explants cultured with vehicle (A, C, E) or 350 ng/mL sildenafil (B, E, F) are shown. Bright-field images (A, B) and paired fields labeled with 6-diamino-2-phenylindole (C, D) or anti-Ki67 (E, F) are included. Size bar in (A) applies to all image panels. Outgrowth length and cell proliferation were measured using Simple PCI image analysis software (G, H). The graph in (G) shows outgrowth lengths for triplicate experiments in which 10 villous explants were measured for each treatment. * P<.05 vs. vehicle. The graph in (H) shows the percentage of cell nuclei in the outgrowth regions that were labeled with anti-Ki67 antibody. The differences between vehicle- and sildenafil-treated explants were not significant (n = 8). Error bars represent SEM.

Journal: Fertility and sterility

Article Title: Sildenafil stimulates human trophoblast invasion through nitric oxide and guanosine 3′,5′-cyclic monophosphate signaling

doi: 10.1016/j.fertnstert.2015.02.025

Figure Lengend Snippet: Trophoblast invasion from first-trimester chorionic villous explants. First-trimester villous explants were cultured on Matrigel-coated transwell inserts and treated with vehicle or 350 ng/mL sildenafil for 72 hours before fixation. Examples of outgrowths from villous explants cultured with vehicle (A, C, E) or 350 ng/mL sildenafil (B, E, F) are shown. Bright-field images (A, B) and paired fields labeled with 6-diamino-2-phenylindole (C, D) or anti-Ki67 (E, F) are included. Size bar in (A) applies to all image panels. Outgrowth length and cell proliferation were measured using Simple PCI image analysis software (G, H). The graph in (G) shows outgrowth lengths for triplicate experiments in which 10 villous explants were measured for each treatment. * P<.05 vs. vehicle. The graph in (H) shows the percentage of cell nuclei in the outgrowth regions that were labeled with anti-Ki67 antibody. The differences between vehicle- and sildenafil-treated explants were not significant (n = 8). Error bars represent SEM.

Article Snippet: Images were processed to determine gray level using Simple PCI (Hamamatsu) imaging software, as previously described ( 31 , 32 ).

Techniques: Cell Culture, Labeling, Software

Semiquantitative assessment and localization of CBS and CSE. UA sections were labeled with antibodies against CBS, or CSE (not shown), followed by secondary Alexa488 (green)-labeled secondary antibody. Endothelial cells were labeled with CD31 followed by Alexa568 (red)-labeled secondary antibody. Cell nuclei were stained with DAPI. Negative control treated with IgG or with primary antibody omitted is shown in first panel. Representative outline of border between UA intima and media was indicated, and UA lumen (l), intima (i), and media (m) were denoted (second panel). Regions of interest for intima (ROI – i) and media (ROI – m) used for analysis in Simple PCI software are illustrated (third panel). Scale bar is 25 μm

Journal: Methods in molecular biology (Clifton, N.J.)

Article Title: Analysis of Vascular Hydrogen Sulfide Biosynthesis

doi: 10.1007/978-1-4939-9528-8_3

Figure Lengend Snippet: Semiquantitative assessment and localization of CBS and CSE. UA sections were labeled with antibodies against CBS, or CSE (not shown), followed by secondary Alexa488 (green)-labeled secondary antibody. Endothelial cells were labeled with CD31 followed by Alexa568 (red)-labeled secondary antibody. Cell nuclei were stained with DAPI. Negative control treated with IgG or with primary antibody omitted is shown in first panel. Representative outline of border between UA intima and media was indicated, and UA lumen (l), intima (i), and media (m) were denoted (second panel). Regions of interest for intima (ROI – i) and media (ROI – m) used for analysis in Simple PCI software are illustrated (third panel). Scale bar is 25 μm

Article Snippet: Image Analysis list-behavior=enumerated prefix-word= mark-type=decimal max-label-size=0 Open image in Simple PCI Image analysis software (Hamamatsu Corp, Sewickley, PA, USA).

Techniques: Labeling, Staining, Negative Control, Software