eclipse c2 system Search Results


99
Nikon digital eclipse nikon c1 confocal laser scanning microscope clsm
Digital Eclipse Nikon C1 Confocal Laser Scanning Microscope Clsm, 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
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Nikon c2 eclipse ti
C2 Eclipse Ti, 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
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Nikon confocal microscope eclipse c2 plus
Confocal Microscope Eclipse C2 Plus, supplied by Nikon, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Nikon c2 confocal head
Validation of HBMVPs and identification of PAs. A: representative images of the expression of α-SMA-, PDGFR-β-, DES-, and CD13-positive HBMVPs. Images were captured with an Eclipse 55i fluorescence microscope connected with a DS-FiL1 color camera (Nikon, Melville, NY) at the magnification of ×850. B: representative image of isolated PAs covered with α-SMA- and PDGFR-β-positive-stained pericytes. Yellow arrows point to α-SMA- and PDGFR-β-positive pericytes. Red and green arrows point to α-SMA- and PDGFR-β-positive pericytes, respectively. The slides were imaged with a Nikon <t>C2+</t> <t>confocal</t> head mounted on an Eclipse Ti2 inverted microscope (Nikon) using a ×60 oil immersion objective (total magnification of ×1,320). DES, desmin; HBMVPs, human brain microvascular pericytes; PAs, parenchymal arterioles; PDGFR-β, platelet-derived growth factor receptor β; α-SMA, α-smooth muscle actin.
C2 Confocal Head, 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
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Average 99 stars, based on 1 article reviews
c2 confocal head - by Bioz Stars, 2026-04
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Nikon eclipse c2 si confocal spectral microscope
Validation of HBMVPs and identification of PAs. A: representative images of the expression of α-SMA-, PDGFR-β-, DES-, and CD13-positive HBMVPs. Images were captured with an Eclipse 55i fluorescence microscope connected with a DS-FiL1 color camera (Nikon, Melville, NY) at the magnification of ×850. B: representative image of isolated PAs covered with α-SMA- and PDGFR-β-positive-stained pericytes. Yellow arrows point to α-SMA- and PDGFR-β-positive pericytes. Red and green arrows point to α-SMA- and PDGFR-β-positive pericytes, respectively. The slides were imaged with a Nikon <t>C2+</t> <t>confocal</t> head mounted on an Eclipse Ti2 inverted microscope (Nikon) using a ×60 oil immersion objective (total magnification of ×1,320). DES, desmin; HBMVPs, human brain microvascular pericytes; PAs, parenchymal arterioles; PDGFR-β, platelet-derived growth factor receptor β; α-SMA, α-smooth muscle actin.
Eclipse C2 Si Confocal Spectral 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
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Nikon eclipse e800 fluorescence microscope
Validation of HBMVPs and identification of PAs. A: representative images of the expression of α-SMA-, PDGFR-β-, DES-, and CD13-positive HBMVPs. Images were captured with an Eclipse 55i fluorescence microscope connected with a DS-FiL1 color camera (Nikon, Melville, NY) at the magnification of ×850. B: representative image of isolated PAs covered with α-SMA- and PDGFR-β-positive-stained pericytes. Yellow arrows point to α-SMA- and PDGFR-β-positive pericytes. Red and green arrows point to α-SMA- and PDGFR-β-positive pericytes, respectively. The slides were imaged with a Nikon <t>C2+</t> <t>confocal</t> head mounted on an Eclipse Ti2 inverted microscope (Nikon) using a ×60 oil immersion objective (total magnification of ×1,320). DES, desmin; HBMVPs, human brain microvascular pericytes; PAs, parenchymal arterioles; PDGFR-β, platelet-derived growth factor receptor β; α-SMA, α-smooth muscle actin.
Eclipse E800 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
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Nikon nikon eclipse c2
Validation of HBMVPs and identification of PAs. A: representative images of the expression of α-SMA-, PDGFR-β-, DES-, and CD13-positive HBMVPs. Images were captured with an Eclipse 55i fluorescence microscope connected with a DS-FiL1 color camera (Nikon, Melville, NY) at the magnification of ×850. B: representative image of isolated PAs covered with α-SMA- and PDGFR-β-positive-stained pericytes. Yellow arrows point to α-SMA- and PDGFR-β-positive pericytes. Red and green arrows point to α-SMA- and PDGFR-β-positive pericytes, respectively. The slides were imaged with a Nikon <t>C2+</t> <t>confocal</t> head mounted on an Eclipse Ti2 inverted microscope (Nikon) using a ×60 oil immersion objective (total magnification of ×1,320). DES, desmin; HBMVPs, human brain microvascular pericytes; PAs, parenchymal arterioles; PDGFR-β, platelet-derived growth factor receptor β; α-SMA, α-smooth muscle actin.
Nikon Eclipse C2, supplied by Nikon, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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90
Nikon eclipse ti inverted fluorescence microscope
Validation of HBMVPs and identification of PAs. A: representative images of the expression of α-SMA-, PDGFR-β-, DES-, and CD13-positive HBMVPs. Images were captured with an Eclipse 55i fluorescence microscope connected with a DS-FiL1 color camera (Nikon, Melville, NY) at the magnification of ×850. B: representative image of isolated PAs covered with α-SMA- and PDGFR-β-positive-stained pericytes. Yellow arrows point to α-SMA- and PDGFR-β-positive pericytes. Red and green arrows point to α-SMA- and PDGFR-β-positive pericytes, respectively. The slides were imaged with a Nikon <t>C2+</t> <t>confocal</t> head mounted on an Eclipse Ti2 inverted microscope (Nikon) using a ×60 oil immersion objective (total magnification of ×1,320). DES, desmin; HBMVPs, human brain microvascular pericytes; PAs, parenchymal arterioles; PDGFR-β, platelet-derived growth factor receptor β; α-SMA, α-smooth muscle actin.
Eclipse Ti Inverted Fluorescence Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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eclipse ti inverted fluorescence microscope - by Bioz Stars, 2026-04
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Nikon ti2a yokogawa w1 spinning disk confocal microscope
Validation of HBMVPs and identification of PAs. A: representative images of the expression of α-SMA-, PDGFR-β-, DES-, and CD13-positive HBMVPs. Images were captured with an Eclipse 55i fluorescence microscope connected with a DS-FiL1 color camera (Nikon, Melville, NY) at the magnification of ×850. B: representative image of isolated PAs covered with α-SMA- and PDGFR-β-positive-stained pericytes. Yellow arrows point to α-SMA- and PDGFR-β-positive pericytes. Red and green arrows point to α-SMA- and PDGFR-β-positive pericytes, respectively. The slides were imaged with a Nikon <t>C2+</t> <t>confocal</t> head mounted on an Eclipse Ti2 inverted microscope (Nikon) using a ×60 oil immersion objective (total magnification of ×1,320). DES, desmin; HBMVPs, human brain microvascular pericytes; PAs, parenchymal arterioles; PDGFR-β, platelet-derived growth factor receptor β; α-SMA, α-smooth muscle actin.
Ti2a Yokogawa W1 Spinning Disk Confocal Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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99
Nikon ni e c2 microscope
Validation of HBMVPs and identification of PAs. A: representative images of the expression of α-SMA-, PDGFR-β-, DES-, and CD13-positive HBMVPs. Images were captured with an Eclipse 55i fluorescence microscope connected with a DS-FiL1 color camera (Nikon, Melville, NY) at the magnification of ×850. B: representative image of isolated PAs covered with α-SMA- and PDGFR-β-positive-stained pericytes. Yellow arrows point to α-SMA- and PDGFR-β-positive pericytes. Red and green arrows point to α-SMA- and PDGFR-β-positive pericytes, respectively. The slides were imaged with a Nikon <t>C2+</t> <t>confocal</t> head mounted on an Eclipse Ti2 inverted microscope (Nikon) using a ×60 oil immersion objective (total magnification of ×1,320). DES, desmin; HBMVPs, human brain microvascular pericytes; PAs, parenchymal arterioles; PDGFR-β, platelet-derived growth factor receptor β; α-SMA, α-smooth muscle actin.
Ni E C2 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
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ni e c2 microscope - by Bioz Stars, 2026-04
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90
Nikon clsm nikon eclipse ni-e c2
Validation of HBMVPs and identification of PAs. A: representative images of the expression of α-SMA-, PDGFR-β-, DES-, and CD13-positive HBMVPs. Images were captured with an Eclipse 55i fluorescence microscope connected with a DS-FiL1 color camera (Nikon, Melville, NY) at the magnification of ×850. B: representative image of isolated PAs covered with α-SMA- and PDGFR-β-positive-stained pericytes. Yellow arrows point to α-SMA- and PDGFR-β-positive pericytes. Red and green arrows point to α-SMA- and PDGFR-β-positive pericytes, respectively. The slides were imaged with a Nikon <t>C2+</t> <t>confocal</t> head mounted on an Eclipse Ti2 inverted microscope (Nikon) using a ×60 oil immersion objective (total magnification of ×1,320). DES, desmin; HBMVPs, human brain microvascular pericytes; PAs, parenchymal arterioles; PDGFR-β, platelet-derived growth factor receptor β; α-SMA, α-smooth muscle actin.
Clsm Nikon Eclipse Ni E C2, supplied by Nikon, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Nikon nikon elements-ar 5.42.02
Validation of HBMVPs and identification of PAs. A: representative images of the expression of α-SMA-, PDGFR-β-, DES-, and CD13-positive HBMVPs. Images were captured with an Eclipse 55i fluorescence microscope connected with a DS-FiL1 color camera (Nikon, Melville, NY) at the magnification of ×850. B: representative image of isolated PAs covered with α-SMA- and PDGFR-β-positive-stained pericytes. Yellow arrows point to α-SMA- and PDGFR-β-positive pericytes. Red and green arrows point to α-SMA- and PDGFR-β-positive pericytes, respectively. The slides were imaged with a Nikon <t>C2+</t> <t>confocal</t> head mounted on an Eclipse Ti2 inverted microscope (Nikon) using a ×60 oil immersion objective (total magnification of ×1,320). DES, desmin; HBMVPs, human brain microvascular pericytes; PAs, parenchymal arterioles; PDGFR-β, platelet-derived growth factor receptor β; α-SMA, α-smooth muscle actin.
Nikon Elements Ar 5.42.02, supplied by Nikon, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Validation of HBMVPs and identification of PAs. A: representative images of the expression of α-SMA-, PDGFR-β-, DES-, and CD13-positive HBMVPs. Images were captured with an Eclipse 55i fluorescence microscope connected with a DS-FiL1 color camera (Nikon, Melville, NY) at the magnification of ×850. B: representative image of isolated PAs covered with α-SMA- and PDGFR-β-positive-stained pericytes. Yellow arrows point to α-SMA- and PDGFR-β-positive pericytes. Red and green arrows point to α-SMA- and PDGFR-β-positive pericytes, respectively. The slides were imaged with a Nikon C2+ confocal head mounted on an Eclipse Ti2 inverted microscope (Nikon) using a ×60 oil immersion objective (total magnification of ×1,320). DES, desmin; HBMVPs, human brain microvascular pericytes; PAs, parenchymal arterioles; PDGFR-β, platelet-derived growth factor receptor β; α-SMA, α-smooth muscle actin.

Journal: American Journal of Physiology - Heart and Circulatory Physiology

Article Title: Reduced pericyte and tight junction coverage in old diabetic rats are associated with hyperglycemia-induced cerebrovascular pericyte dysfunction

doi: 10.1152/ajpheart.00726.2020

Figure Lengend Snippet: Validation of HBMVPs and identification of PAs. A: representative images of the expression of α-SMA-, PDGFR-β-, DES-, and CD13-positive HBMVPs. Images were captured with an Eclipse 55i fluorescence microscope connected with a DS-FiL1 color camera (Nikon, Melville, NY) at the magnification of ×850. B: representative image of isolated PAs covered with α-SMA- and PDGFR-β-positive-stained pericytes. Yellow arrows point to α-SMA- and PDGFR-β-positive pericytes. Red and green arrows point to α-SMA- and PDGFR-β-positive pericytes, respectively. The slides were imaged with a Nikon C2+ confocal head mounted on an Eclipse Ti2 inverted microscope (Nikon) using a ×60 oil immersion objective (total magnification of ×1,320). DES, desmin; HBMVPs, human brain microvascular pericytes; PAs, parenchymal arterioles; PDGFR-β, platelet-derived growth factor receptor β; α-SMA, α-smooth muscle actin.

Article Snippet: The slides were imaged with a Nikon C2+ confocal head mounted on an Eclipse Ti2 inverted microscope (Nikon) using a ×60 oil immersion objective (total magnification of ×1,320).

Techniques: Expressing, Fluorescence, Microscopy, Isolation, Staining, Inverted Microscopy, Derivative Assay