ez-c1 confocal software Search Results


spectral c1 confocal microscope  (Nikon)
99
Nikon spectral c1 confocal microscope
Spectral C1 Confocal Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ez-c1+confocal+software/C2%2B/pmc05967305-214-26-30
Average 99 stars, based on 1 article reviews
spectral c1 confocal microscope - by Bioz Stars, 2026-10
99/100 stars
  Buy from Supplier
laser scanning confocal microscopy  (Nikon)
99
Nikon laser scanning confocal microscopy
Figure 1. Characterization of IPEC-J2 cell monolayer. (A) Light microscope image of confluent cell monolayer grown on a tissue culture flask, scale bar equals 20 lm. (B) Confocal micrograph showing a top view of IPEC-J2 monolayer grown on transwell filter for 9 days, the cell borders can be distinguished by immunofluorescent staining of tight junction protein ZO-1, scale bar equals 20 lm. (C) Top view of well- differentiated IPEC-J2 cell with microvilli observed by scanning electron <t>microscopy,</t> figure contains one cell from cell monolayer grown on transwell filter for 9 days, scale bar equals 5 lm. (D) Progression in transepithelial electrical resistance (TEER) values of cells grown on transwell filter for 9 days. Data are given as means (SEM) of 20 separate experiments. They were assigned to experimental treatment on day 9, respectively.
Laser Scanning Confocal Microscopy, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ez-c1+confocal+software/Objectives/pm25847917-141-4-8
Average 99 stars, based on 1 article reviews
laser scanning confocal microscopy - by Bioz Stars, 2026-10
99/100 stars
  Buy from Supplier
c2  (Nikon)
99
Nikon c2
Figure 1. Characterization of IPEC-J2 cell monolayer. (A) Light microscope image of confluent cell monolayer grown on a tissue culture flask, scale bar equals 20 lm. (B) Confocal micrograph showing a top view of IPEC-J2 monolayer grown on transwell filter for 9 days, the cell borders can be distinguished by immunofluorescent staining of tight junction protein ZO-1, scale bar equals 20 lm. (C) Top view of well- differentiated IPEC-J2 cell with microvilli observed by scanning electron <t>microscopy,</t> figure contains one cell from cell monolayer grown on transwell filter for 9 days, scale bar equals 5 lm. (D) Progression in transepithelial electrical resistance (TEER) values of cells grown on transwell filter for 9 days. Data are given as means (SEM) of 20 separate experiments. They were assigned to experimental treatment on day 9, respectively.
C2, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ez-c1+confocal+software/NIS-Elements/pmc05303661-107-14-13
Average 99 stars, based on 1 article reviews
c2 - by Bioz Stars, 2026-10
99/100 stars
  Buy from Supplier
nikon ez-c1 acquisition software  (Image Systems Inc)
90
Image Systems Inc nikon ez-c1 acquisition software
Figure 1. Characterization of IPEC-J2 cell monolayer. (A) Light microscope image of confluent cell monolayer grown on a tissue culture flask, scale bar equals 20 lm. (B) Confocal micrograph showing a top view of IPEC-J2 monolayer grown on transwell filter for 9 days, the cell borders can be distinguished by immunofluorescent staining of tight junction protein ZO-1, scale bar equals 20 lm. (C) Top view of well- differentiated IPEC-J2 cell with microvilli observed by scanning electron <t>microscopy,</t> figure contains one cell from cell monolayer grown on transwell filter for 9 days, scale bar equals 5 lm. (D) Progression in transepithelial electrical resistance (TEER) values of cells grown on transwell filter for 9 days. Data are given as means (SEM) of 20 separate experiments. They were assigned to experimental treatment on day 9, respectively.
Nikon Ez C1 Acquisition Software, supplied by Image Systems 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/ez-c1+confocal+software/nikon+ez+c1+software/pmc02525806-117-12-18
Average 90 stars, based on 1 article reviews
nikon ez-c1 acquisition software - by Bioz Stars, 2026-10
90/100 stars
  Buy from Supplier
imaris  (Oxford Instruments)
99
Oxford Instruments imaris
Figure 1. Characterization of IPEC-J2 cell monolayer. (A) Light microscope image of confluent cell monolayer grown on a tissue culture flask, scale bar equals 20 lm. (B) Confocal micrograph showing a top view of IPEC-J2 monolayer grown on transwell filter for 9 days, the cell borders can be distinguished by immunofluorescent staining of tight junction protein ZO-1, scale bar equals 20 lm. (C) Top view of well- differentiated IPEC-J2 cell with microvilli observed by scanning electron <t>microscopy,</t> figure contains one cell from cell monolayer grown on transwell filter for 9 days, scale bar equals 5 lm. (D) Progression in transepithelial electrical resistance (TEER) values of cells grown on transwell filter for 9 days. Data are given as means (SEM) of 20 separate experiments. They were assigned to experimental treatment on day 9, respectively.
Imaris, supplied by Oxford Instruments, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ez-c1+confocal+software/Imaris/custom%40imaris%4026191537
Average 99 stars, based on 1 article reviews
imaris - by Bioz Stars, 2026-10
99/100 stars
  Buy from Supplier
nykon c1si confocal microscope  (Nycon Corporation)
90
Nycon Corporation nykon c1si confocal microscope
Figure 1. Characterization of IPEC-J2 cell monolayer. (A) Light microscope image of confluent cell monolayer grown on a tissue culture flask, scale bar equals 20 lm. (B) Confocal micrograph showing a top view of IPEC-J2 monolayer grown on transwell filter for 9 days, the cell borders can be distinguished by immunofluorescent staining of tight junction protein ZO-1, scale bar equals 20 lm. (C) Top view of well- differentiated IPEC-J2 cell with microvilli observed by scanning electron <t>microscopy,</t> figure contains one cell from cell monolayer grown on transwell filter for 9 days, scale bar equals 5 lm. (D) Progression in transepithelial electrical resistance (TEER) values of cells grown on transwell filter for 9 days. Data are given as means (SEM) of 20 separate experiments. They were assigned to experimental treatment on day 9, respectively.
Nykon C1si Confocal Microscope, supplied by Nycon 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/ez-c1+confocal+software/nykon+c1si+confocal+microscope/10__1161_slash_circresaha__107__169664-181-5-12
Average 90 stars, based on 1 article reviews
nykon c1si confocal microscope - by Bioz Stars, 2026-10
90/100 stars
  Buy from Supplier
light and fluorescence microscope bz-x700  (KEYENCE)
90
KEYENCE light and fluorescence microscope bz-x700
Figure 1. Characterization of IPEC-J2 cell monolayer. (A) Light microscope image of confluent cell monolayer grown on a tissue culture flask, scale bar equals 20 lm. (B) Confocal micrograph showing a top view of IPEC-J2 monolayer grown on transwell filter for 9 days, the cell borders can be distinguished by immunofluorescent staining of tight junction protein ZO-1, scale bar equals 20 lm. (C) Top view of well- differentiated IPEC-J2 cell with microvilli observed by scanning electron <t>microscopy,</t> figure contains one cell from cell monolayer grown on transwell filter for 9 days, scale bar equals 5 lm. (D) Progression in transepithelial electrical resistance (TEER) values of cells grown on transwell filter for 9 days. Data are given as means (SEM) of 20 separate experiments. They were assigned to experimental treatment on day 9, respectively.
Light And Fluorescence Microscope Bz X700, supplied by KEYENCE, 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/ez-c1+confocal+software/fluorescence+microscope+bz+9000/pmc12143657-390-19-22
Average 90 stars, based on 1 article reviews
light and fluorescence microscope bz-x700 - by Bioz Stars, 2026-10
90/100 stars
  Buy from Supplier
mowiol  (Carl Roth GmbH)
90
Carl Roth GmbH mowiol
Figure 1. Characterization of IPEC-J2 cell monolayer. (A) Light microscope image of confluent cell monolayer grown on a tissue culture flask, scale bar equals 20 lm. (B) Confocal micrograph showing a top view of IPEC-J2 monolayer grown on transwell filter for 9 days, the cell borders can be distinguished by immunofluorescent staining of tight junction protein ZO-1, scale bar equals 20 lm. (C) Top view of well- differentiated IPEC-J2 cell with microvilli observed by scanning electron <t>microscopy,</t> figure contains one cell from cell monolayer grown on transwell filter for 9 days, scale bar equals 5 lm. (D) Progression in transepithelial electrical resistance (TEER) values of cells grown on transwell filter for 9 days. Data are given as means (SEM) of 20 separate experiments. They were assigned to experimental treatment on day 9, respectively.
Mowiol, supplied by Carl Roth GmbH, 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/ez-c1+confocal+software/mowiol/pm23650619-175-3-4
Average 90 stars, based on 1 article reviews
mowiol - by Bioz Stars, 2026-10
90/100 stars
  Buy from Supplier
aqua-poly/mount  (Polysciences inc)
90
Polysciences inc aqua-poly/mount
Figure 1. Characterization of IPEC-J2 cell monolayer. (A) Light microscope image of confluent cell monolayer grown on a tissue culture flask, scale bar equals 20 lm. (B) Confocal micrograph showing a top view of IPEC-J2 monolayer grown on transwell filter for 9 days, the cell borders can be distinguished by immunofluorescent staining of tight junction protein ZO-1, scale bar equals 20 lm. (C) Top view of well- differentiated IPEC-J2 cell with microvilli observed by scanning electron <t>microscopy,</t> figure contains one cell from cell monolayer grown on transwell filter for 9 days, scale bar equals 5 lm. (D) Progression in transepithelial electrical resistance (TEER) values of cells grown on transwell filter for 9 days. Data are given as means (SEM) of 20 separate experiments. They were assigned to experimental treatment on day 9, respectively.
Aqua Poly/Mount, supplied by Polysciences 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/ez-c1+confocal+software/aqua+poly+mount/pmc06831210-124-6-7
Average 90 stars, based on 1 article reviews
aqua-poly/mount - by Bioz Stars, 2026-10
90/100 stars
  Buy from Supplier
fluorescence inverted microscope  (Nikon)
99
Nikon fluorescence inverted microscope
Figure 1. Characterization of IPEC-J2 cell monolayer. (A) Light microscope image of confluent cell monolayer grown on a tissue culture flask, scale bar equals 20 lm. (B) Confocal micrograph showing a top view of IPEC-J2 monolayer grown on transwell filter for 9 days, the cell borders can be distinguished by immunofluorescent staining of tight junction protein ZO-1, scale bar equals 20 lm. (C) Top view of well- differentiated IPEC-J2 cell with microvilli observed by scanning electron <t>microscopy,</t> figure contains one cell from cell monolayer grown on transwell filter for 9 days, scale bar equals 5 lm. (D) Progression in transepithelial electrical resistance (TEER) values of cells grown on transwell filter for 9 days. Data are given as means (SEM) of 20 separate experiments. They were assigned to experimental treatment on day 9, respectively.
Fluorescence Inverted Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ez-c1+confocal+software/Inverted+Microscopes/pmc04070317-170-8-13
Average 99 stars, based on 1 article reviews
fluorescence inverted microscope - by Bioz Stars, 2026-10
99/100 stars
  Buy from Supplier
nikon eclipse te2000  (Nikon)
99
Nikon nikon eclipse te2000
Figure 1. Characterization of IPEC-J2 cell monolayer. (A) Light microscope image of confluent cell monolayer grown on a tissue culture flask, scale bar equals 20 lm. (B) Confocal micrograph showing a top view of IPEC-J2 monolayer grown on transwell filter for 9 days, the cell borders can be distinguished by immunofluorescent staining of tight junction protein ZO-1, scale bar equals 20 lm. (C) Top view of well- differentiated IPEC-J2 cell with microvilli observed by scanning electron <t>microscopy,</t> figure contains one cell from cell monolayer grown on transwell filter for 9 days, scale bar equals 5 lm. (D) Progression in transepithelial electrical resistance (TEER) values of cells grown on transwell filter for 9 days. Data are given as means (SEM) of 20 separate experiments. They were assigned to experimental treatment on day 9, respectively.
Nikon Eclipse Te2000, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ez-c1+confocal+software/ECLIPSE+E200/pm35393558-120-14-14
Average 99 stars, based on 1 article reviews
nikon eclipse te2000 - by Bioz Stars, 2026-10
99/100 stars
  Buy from Supplier
orca ccd camera  (Hamamatsu)
90
Hamamatsu orca ccd camera
Figure 1. Characterization of IPEC-J2 cell monolayer. (A) Light microscope image of confluent cell monolayer grown on a tissue culture flask, scale bar equals 20 lm. (B) Confocal micrograph showing a top view of IPEC-J2 monolayer grown on transwell filter for 9 days, the cell borders can be distinguished by immunofluorescent staining of tight junction protein ZO-1, scale bar equals 20 lm. (C) Top view of well- differentiated IPEC-J2 cell with microvilli observed by scanning electron <t>microscopy,</t> figure contains one cell from cell monolayer grown on transwell filter for 9 days, scale bar equals 5 lm. (D) Progression in transepithelial electrical resistance (TEER) values of cells grown on transwell filter for 9 days. Data are given as means (SEM) of 20 separate experiments. They were assigned to experimental treatment on day 9, respectively.
Orca Ccd Camera, supplied by Hamamatsu, 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/ez-c1+confocal+software/orca+er+camera/pmc02944843-185-13-12
Average 90 stars, based on 1 article reviews
orca ccd camera - by Bioz Stars, 2026-10
90/100 stars
  Buy from Supplier

Image Search Results


Figure 1. Characterization of IPEC-J2 cell monolayer. (A) Light microscope image of confluent cell monolayer grown on a tissue culture flask, scale bar equals 20 lm. (B) Confocal micrograph showing a top view of IPEC-J2 monolayer grown on transwell filter for 9 days, the cell borders can be distinguished by immunofluorescent staining of tight junction protein ZO-1, scale bar equals 20 lm. (C) Top view of well- differentiated IPEC-J2 cell with microvilli observed by scanning electron microscopy, figure contains one cell from cell monolayer grown on transwell filter for 9 days, scale bar equals 5 lm. (D) Progression in transepithelial electrical resistance (TEER) values of cells grown on transwell filter for 9 days. Data are given as means (SEM) of 20 separate experiments. They were assigned to experimental treatment on day 9, respectively.

Journal: Physiological reports

Article Title: Effects of Lactobacillus johnsonii and Lactobacillus reuteri on gut barrier function and heat shock proteins in intestinal porcine epithelial cells.

doi: 10.14814/phy2.12355

Figure Lengend Snippet: Figure 1. Characterization of IPEC-J2 cell monolayer. (A) Light microscope image of confluent cell monolayer grown on a tissue culture flask, scale bar equals 20 lm. (B) Confocal micrograph showing a top view of IPEC-J2 monolayer grown on transwell filter for 9 days, the cell borders can be distinguished by immunofluorescent staining of tight junction protein ZO-1, scale bar equals 20 lm. (C) Top view of well- differentiated IPEC-J2 cell with microvilli observed by scanning electron microscopy, figure contains one cell from cell monolayer grown on transwell filter for 9 days, scale bar equals 5 lm. (D) Progression in transepithelial electrical resistance (TEER) values of cells grown on transwell filter for 9 days. Data are given as means (SEM) of 20 separate experiments. They were assigned to experimental treatment on day 9, respectively.

Article Snippet: Images were acquired using laser scanning confocal microscopy (Nikon C-1 with Plan ApoVC 609/1.40 oil objective; Nikon EZ-C1 software; Nikon, Amsterdam, the Netherlands).

Techniques: Light Microscopy, Staining, Electron Microscopy

Figure 7. Cellular distribution of the tight junction protein ZO-1 in IPEC-J2 cells. Cell monolayers grown on transwell filters were left untreated (control) or treated with bacterial cells of ETEC (multiplicity of infection, MOI 10) alone for 3 h or pretreated with Lactobacillus spp. (MOI 100) for 6 h and then challenged by ETEC for 3 h. Monolayers stained for the tight junction protein ZO-1 (green) and nuclei stained with DAPI (blue) were detected by laser scanning confocal microscopy. The images were representatives from three separate experiments. Yellow arrows show the broken lining of ZO-1 expressions. Red circles highlight areas of cell disassociation. Scale bar equals 50 lm for all images.

Journal: Physiological reports

Article Title: Effects of Lactobacillus johnsonii and Lactobacillus reuteri on gut barrier function and heat shock proteins in intestinal porcine epithelial cells.

doi: 10.14814/phy2.12355

Figure Lengend Snippet: Figure 7. Cellular distribution of the tight junction protein ZO-1 in IPEC-J2 cells. Cell monolayers grown on transwell filters were left untreated (control) or treated with bacterial cells of ETEC (multiplicity of infection, MOI 10) alone for 3 h or pretreated with Lactobacillus spp. (MOI 100) for 6 h and then challenged by ETEC for 3 h. Monolayers stained for the tight junction protein ZO-1 (green) and nuclei stained with DAPI (blue) were detected by laser scanning confocal microscopy. The images were representatives from three separate experiments. Yellow arrows show the broken lining of ZO-1 expressions. Red circles highlight areas of cell disassociation. Scale bar equals 50 lm for all images.

Article Snippet: Images were acquired using laser scanning confocal microscopy (Nikon C-1 with Plan ApoVC 609/1.40 oil objective; Nikon EZ-C1 software; Nikon, Amsterdam, the Netherlands).

Techniques: Control, Infection, Staining, Confocal Microscopy