d-eclipse c1 laser-scanning confocal system Search Results


laser scanning nikon d eclipse c1 confocal system  (Nikon)
99
Nikon laser scanning nikon d eclipse c1 confocal system
Laser Scanning Nikon D Eclipse C1 Confocal System, 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/d-eclipse+c1+laser-scanning+confocal+system/C2%2B/pm31611573-226-26-27
Average 99 stars, based on 1 article reviews
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d eclipse 80i confocal laser scanning microscope  (Nikon)
99
Nikon d eclipse 80i confocal laser scanning microscope
D Eclipse 80i Confocal Laser Scanning 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/d-eclipse+c1+laser-scanning+confocal+system/Objectives/pmc12236268-58-11-16
Average 99 stars, based on 1 article reviews
d eclipse 80i confocal laser scanning microscope - by Bioz Stars, 2026-09
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bit software  (Nikon)
99
Nikon bit software
Bit Software, 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/d-eclipse+c1+laser-scanning+confocal+system/NIS-Elements/pmc03534029-53-21-17
Average 99 stars, based on 1 article reviews
bit software - by Bioz Stars, 2026-09
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corel draw x6  (corel corporation)
90
corel corporation corel draw x6
Corel Draw X6, supplied by corel 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/d-eclipse+c1+laser-scanning+confocal+system/coreldraw+x7/pmc04418484-98-27-30
Average 90 stars, based on 1 article reviews
corel draw x6 - by Bioz Stars, 2026-09
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intensilight c hgfie fiber illuminator  (Nikon)
96
Nikon intensilight c hgfie fiber illuminator
Intensilight C Hgfie Fiber Illuminator, supplied by Nikon, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/d-eclipse+c1+laser-scanning+confocal+system/Intensilight/pm38182793-281-13-17
Average 96 stars, based on 1 article reviews
intensilight c hgfie fiber illuminator - by Bioz Stars, 2026-09
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inverted fluorescence microscope  (Nikon)
99
Nikon inverted fluorescence microscope
FIG. 1. Uptake of rMP65 fluor by different cell types. (A) MN, MDM, DC, PMN, and PBL treated for 30 min at 37°C with rMP65 fluor (5 g/ml) or rCpPLD fluor (5 g/ml) were analyzed by flow cytometry to assess rMP65 and rCpPLD uptake. The rMP65 fluor uptake by different cell types is expressed as the mean fluorescence intensity (MFI). Data are expressed as means SEM for three independent experiments. *, P 0.05; **, P 0.001 (rMP65 fluor-treated cells versus rCpPLD fluor-treated cells). (B) rMP65 fluor, nMP65 fluor, and rCpPLD fluor uptake by DC, tested using confocal microscopy. DC were treated with 25 g/ml of rMP65 fluor, rCpPLD fluor, or nMP65 fluor for 2 h at 37°C. The cells were then fixed and analyzed with a confocal <t>microscope.</t> (C) MDM or DC were stimulated for 30 min at 37°C with different concentrations of rMP65 fluor (0.5, 1, 2.5, 5, 25, and 50 g/ml). The rMP65 fluor uptake by different cell types is expressed as the MFI. Data are expressed as means SEM for three independent experiments. *, P 0.05; **, P 0.001 (rMP65-treated cells versus untreated cells). (D) MDM were pretreated with various concentrations of RGDS or control peptide for 15 min, and then rMP65 fluor (25 g/ml) was added. Data are expressed as means SEM for three independent experiments. *, P 0.05 (RGDS-treated cells versus untreated cells).
Inverted Fluorescence 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/d-eclipse+c1+laser-scanning+confocal+system/Inverted+Microscopes/10__1128_slash_iai__00669___08-86-17-20
Average 99 stars, based on 1 article reviews
inverted fluorescence microscope - by Bioz Stars, 2026-09
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odyssey  (LI-COR)
99
LI-COR odyssey
FIG. 1. Uptake of rMP65 fluor by different cell types. (A) MN, MDM, DC, PMN, and PBL treated for 30 min at 37°C with rMP65 fluor (5 g/ml) or rCpPLD fluor (5 g/ml) were analyzed by flow cytometry to assess rMP65 and rCpPLD uptake. The rMP65 fluor uptake by different cell types is expressed as the mean fluorescence intensity (MFI). Data are expressed as means SEM for three independent experiments. *, P 0.05; **, P 0.001 (rMP65 fluor-treated cells versus rCpPLD fluor-treated cells). (B) rMP65 fluor, nMP65 fluor, and rCpPLD fluor uptake by DC, tested using confocal microscopy. DC were treated with 25 g/ml of rMP65 fluor, rCpPLD fluor, or nMP65 fluor for 2 h at 37°C. The cells were then fixed and analyzed with a confocal <t>microscope.</t> (C) MDM or DC were stimulated for 30 min at 37°C with different concentrations of rMP65 fluor (0.5, 1, 2.5, 5, 25, and 50 g/ml). The rMP65 fluor uptake by different cell types is expressed as the MFI. Data are expressed as means SEM for three independent experiments. *, P 0.05; **, P 0.001 (rMP65-treated cells versus untreated cells). (D) MDM were pretreated with various concentrations of RGDS or control peptide for 15 min, and then rMP65 fluor (25 g/ml) was added. Data are expressed as means SEM for three independent experiments. *, P 0.05 (RGDS-treated cells versus untreated cells).
Odyssey, supplied by LI-COR, 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/d-eclipse+c1+laser-scanning+confocal+system/Odyssey/custom%40Odyssey%4037598266
Average 99 stars, based on 1 article reviews
odyssey - by Bioz Stars, 2026-09
99/100 stars
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odyssey imaging system  (LI-COR)
99
LI-COR odyssey imaging system
FIG. 1. Uptake of rMP65 fluor by different cell types. (A) MN, MDM, DC, PMN, and PBL treated for 30 min at 37°C with rMP65 fluor (5 g/ml) or rCpPLD fluor (5 g/ml) were analyzed by flow cytometry to assess rMP65 and rCpPLD uptake. The rMP65 fluor uptake by different cell types is expressed as the mean fluorescence intensity (MFI). Data are expressed as means SEM for three independent experiments. *, P 0.05; **, P 0.001 (rMP65 fluor-treated cells versus rCpPLD fluor-treated cells). (B) rMP65 fluor, nMP65 fluor, and rCpPLD fluor uptake by DC, tested using confocal microscopy. DC were treated with 25 g/ml of rMP65 fluor, rCpPLD fluor, or nMP65 fluor for 2 h at 37°C. The cells were then fixed and analyzed with a confocal <t>microscope.</t> (C) MDM or DC were stimulated for 30 min at 37°C with different concentrations of rMP65 fluor (0.5, 1, 2.5, 5, 25, and 50 g/ml). The rMP65 fluor uptake by different cell types is expressed as the MFI. Data are expressed as means SEM for three independent experiments. *, P 0.05; **, P 0.001 (rMP65-treated cells versus untreated cells). (D) MDM were pretreated with various concentrations of RGDS or control peptide for 15 min, and then rMP65 fluor (25 g/ml) was added. Data are expressed as means SEM for three independent experiments. *, P 0.05 (RGDS-treated cells versus untreated cells).
Odyssey Imaging System, supplied by LI-COR, 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/d-eclipse+c1+laser-scanning+confocal+system/Odyssey+Imaging+System/custom%40odyssey-imaging-system%4037598266
Average 99 stars, based on 1 article reviews
odyssey imaging system - by Bioz Stars, 2026-09
99/100 stars
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em-ccd digital camera c9100  (Hamamatsu)
90
Hamamatsu em-ccd digital camera c9100
FIG. 1. Uptake of rMP65 fluor by different cell types. (A) MN, MDM, DC, PMN, and PBL treated for 30 min at 37°C with rMP65 fluor (5 g/ml) or rCpPLD fluor (5 g/ml) were analyzed by flow cytometry to assess rMP65 and rCpPLD uptake. The rMP65 fluor uptake by different cell types is expressed as the mean fluorescence intensity (MFI). Data are expressed as means SEM for three independent experiments. *, P 0.05; **, P 0.001 (rMP65 fluor-treated cells versus rCpPLD fluor-treated cells). (B) rMP65 fluor, nMP65 fluor, and rCpPLD fluor uptake by DC, tested using confocal microscopy. DC were treated with 25 g/ml of rMP65 fluor, rCpPLD fluor, or nMP65 fluor for 2 h at 37°C. The cells were then fixed and analyzed with a confocal <t>microscope.</t> (C) MDM or DC were stimulated for 30 min at 37°C with different concentrations of rMP65 fluor (0.5, 1, 2.5, 5, 25, and 50 g/ml). The rMP65 fluor uptake by different cell types is expressed as the MFI. Data are expressed as means SEM for three independent experiments. *, P 0.05; **, P 0.001 (rMP65-treated cells versus untreated cells). (D) MDM were pretreated with various concentrations of RGDS or control peptide for 15 min, and then rMP65 fluor (25 g/ml) was added. Data are expressed as means SEM for three independent experiments. *, P 0.05 (RGDS-treated cells versus untreated cells).
Em Ccd Digital Camera C9100, 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/d-eclipse+c1+laser-scanning+confocal+system/em+ccd+camera/pmc04494165-65-29-33
Average 90 stars, based on 1 article reviews
em-ccd digital camera c9100 - by Bioz Stars, 2026-09
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glass bottom culture dish  (MatTek)
90
MatTek glass bottom culture dish
FIG. 1. Uptake of rMP65 fluor by different cell types. (A) MN, MDM, DC, PMN, and PBL treated for 30 min at 37°C with rMP65 fluor (5 g/ml) or rCpPLD fluor (5 g/ml) were analyzed by flow cytometry to assess rMP65 and rCpPLD uptake. The rMP65 fluor uptake by different cell types is expressed as the mean fluorescence intensity (MFI). Data are expressed as means SEM for three independent experiments. *, P 0.05; **, P 0.001 (rMP65 fluor-treated cells versus rCpPLD fluor-treated cells). (B) rMP65 fluor, nMP65 fluor, and rCpPLD fluor uptake by DC, tested using confocal microscopy. DC were treated with 25 g/ml of rMP65 fluor, rCpPLD fluor, or nMP65 fluor for 2 h at 37°C. The cells were then fixed and analyzed with a confocal <t>microscope.</t> (C) MDM or DC were stimulated for 30 min at 37°C with different concentrations of rMP65 fluor (0.5, 1, 2.5, 5, 25, and 50 g/ml). The rMP65 fluor uptake by different cell types is expressed as the MFI. Data are expressed as means SEM for three independent experiments. *, P 0.05; **, P 0.001 (rMP65-treated cells versus untreated cells). (D) MDM were pretreated with various concentrations of RGDS or control peptide for 15 min, and then rMP65 fluor (25 g/ml) was added. Data are expressed as means SEM for three independent experiments. *, P 0.05 (RGDS-treated cells versus untreated cells).
Glass Bottom Culture Dish, supplied by MatTek, 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/d-eclipse+c1+laser-scanning+confocal+system/glass+bottom+culture+dishes/pmc04192541-77-22-26
Average 90 stars, based on 1 article reviews
glass bottom culture dish - by Bioz Stars, 2026-09
90/100 stars
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facscalibur flow cytometer  (Becton Dickinson)
90
Becton Dickinson facscalibur flow cytometer
FIG. 1. Uptake of rMP65 fluor by different cell types. (A) MN, MDM, DC, PMN, and PBL treated for 30 min at 37°C with rMP65 fluor (5 g/ml) or rCpPLD fluor (5 g/ml) were analyzed by flow cytometry to assess rMP65 and rCpPLD uptake. The rMP65 fluor uptake by different cell types is expressed as the mean fluorescence intensity (MFI). Data are expressed as means SEM for three independent experiments. *, P 0.05; **, P 0.001 (rMP65 fluor-treated cells versus rCpPLD fluor-treated cells). (B) rMP65 fluor, nMP65 fluor, and rCpPLD fluor uptake by DC, tested using confocal microscopy. DC were treated with 25 g/ml of rMP65 fluor, rCpPLD fluor, or nMP65 fluor for 2 h at 37°C. The cells were then fixed and analyzed with a confocal <t>microscope.</t> (C) MDM or DC were stimulated for 30 min at 37°C with different concentrations of rMP65 fluor (0.5, 1, 2.5, 5, 25, and 50 g/ml). The rMP65 fluor uptake by different cell types is expressed as the MFI. Data are expressed as means SEM for three independent experiments. *, P 0.05; **, P 0.001 (rMP65-treated cells versus untreated cells). (D) MDM were pretreated with various concentrations of RGDS or control peptide for 15 min, and then rMP65 fluor (25 g/ml) was added. Data are expressed as means SEM for three independent experiments. *, P 0.05 (RGDS-treated cells versus untreated cells).
Facscalibur Flow Cytometer, 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
https://www.bioz.com/product/d-eclipse+c1+laser-scanning+confocal+system/facscalibur+flow+cytometer/pmc03633907-53-40-43
Average 90 stars, based on 1 article reviews
facscalibur flow cytometer - by Bioz Stars, 2026-09
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Image Search Results


FIG. 1. Uptake of rMP65 fluor by different cell types. (A) MN, MDM, DC, PMN, and PBL treated for 30 min at 37°C with rMP65 fluor (5 g/ml) or rCpPLD fluor (5 g/ml) were analyzed by flow cytometry to assess rMP65 and rCpPLD uptake. The rMP65 fluor uptake by different cell types is expressed as the mean fluorescence intensity (MFI). Data are expressed as means SEM for three independent experiments. *, P 0.05; **, P 0.001 (rMP65 fluor-treated cells versus rCpPLD fluor-treated cells). (B) rMP65 fluor, nMP65 fluor, and rCpPLD fluor uptake by DC, tested using confocal microscopy. DC were treated with 25 g/ml of rMP65 fluor, rCpPLD fluor, or nMP65 fluor for 2 h at 37°C. The cells were then fixed and analyzed with a confocal microscope. (C) MDM or DC were stimulated for 30 min at 37°C with different concentrations of rMP65 fluor (0.5, 1, 2.5, 5, 25, and 50 g/ml). The rMP65 fluor uptake by different cell types is expressed as the MFI. Data are expressed as means SEM for three independent experiments. *, P 0.05; **, P 0.001 (rMP65-treated cells versus untreated cells). (D) MDM were pretreated with various concentrations of RGDS or control peptide for 15 min, and then rMP65 fluor (25 g/ml) was added. Data are expressed as means SEM for three independent experiments. *, P 0.05 (RGDS-treated cells versus untreated cells).

Journal: Infection and Immunity

Article Title: A Candida albicans Mannoprotein Deprived of Its Mannan Moiety Is Efficiently Taken Up and Processed by Human Dendritic Cells and Induces T-Cell Activation without Stimulating Proinflammatory Cytokine Production

doi: 10.1128/iai.00669-08

Figure Lengend Snippet: FIG. 1. Uptake of rMP65 fluor by different cell types. (A) MN, MDM, DC, PMN, and PBL treated for 30 min at 37°C with rMP65 fluor (5 g/ml) or rCpPLD fluor (5 g/ml) were analyzed by flow cytometry to assess rMP65 and rCpPLD uptake. The rMP65 fluor uptake by different cell types is expressed as the mean fluorescence intensity (MFI). Data are expressed as means SEM for three independent experiments. *, P 0.05; **, P 0.001 (rMP65 fluor-treated cells versus rCpPLD fluor-treated cells). (B) rMP65 fluor, nMP65 fluor, and rCpPLD fluor uptake by DC, tested using confocal microscopy. DC were treated with 25 g/ml of rMP65 fluor, rCpPLD fluor, or nMP65 fluor for 2 h at 37°C. The cells were then fixed and analyzed with a confocal microscope. (C) MDM or DC were stimulated for 30 min at 37°C with different concentrations of rMP65 fluor (0.5, 1, 2.5, 5, 25, and 50 g/ml). The rMP65 fluor uptake by different cell types is expressed as the MFI. Data are expressed as means SEM for three independent experiments. *, P 0.05; **, P 0.001 (rMP65-treated cells versus untreated cells). (D) MDM were pretreated with various concentrations of RGDS or control peptide for 15 min, and then rMP65 fluor (25 g/ml) was added. Data are expressed as means SEM for three independent experiments. *, P 0.05 (RGDS-treated cells versus untreated cells).

Article Snippet: Images were collected on a Nikon C1 laser scanning confocal unit (Nikon D-Eclipse C1) attached to an inverted fluorescence microscope (Nikon Eclipse TE 2000-U).

Techniques: Cytometry, Confocal Microscopy, Microscopy, Control