digital imaging fluorescence microscopy systems Search Results


99
Evident Corporation fluorescence microscope
Fluorescence Microscope, supplied by Evident Corporation, 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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MetaMorph Inc fluorescence microscopy metamorph imaging system analysis
Fluorescence Microscopy Metamorph Imaging System Analysis, supplied by MetaMorph Inc, 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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KEYENCE digital images under optical and fluorescence microscopy biozero
Digital Images Under Optical And Fluorescence Microscopy Biozero, 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
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Mauna Kea Technologies intravital fiberoptic confocal fluorescence microscopy cellvizioh system
Intravital Fiberoptic Confocal Fluorescence Microscopy Cellvizioh System, supplied by Mauna Kea Technologies, 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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BioImaging Solutions Inc custom-built fluorescence-based digital image microscopy system dimscan
Custom Built Fluorescence Based Digital Image Microscopy System Dimscan, supplied by BioImaging Solutions Inc, 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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Evident Corporation spinning disk fluorescent microscopy image system
Silencing effects of pERK2 and caspase 3 with siRNA after excitotoxic SCI. (A, B, and C): Intrathecal pre-treatment for 72 h with ERK2 siRNA (B and C light bar, 2.5 μg) complexed with lipofectamine 2000 (5 μg) resulted in significant decrease in pERK2 protein expression 4 h after excitotoxic SCI, compared to control siRNA pretreatment (A and C dark bar, 2.5 μg). (D, E, and F): Intrathecal pre-treatment for 72 h with ERK2 siRNA (E and F light bar, 2.5 μg) complexed with lipofectamine 2000 (5 μg) resulted in significant decrease in caspase 3 activity (cleaved caspase 3) 4 h after excitotoxic SCI, compared to control siRNA pretreatment (D and F dark bar, 2.5 μg). The <t>fluorescent</t> labeled pERK2-positive or cleaved caspase 3-positive cells in the QUIS injection epicenter were counted using fliorescent <t>microscopy</t> <t>image</t> <t>system</t> (n=3 sections sparated 60 μm apart per animal, n=3 animals per group). Data were presented as mean ± S.E.M. and analyzed by t-test **p<0.01 and ***p<0.001, t test. Scale bar: 30 μm.
Spinning Disk Fluorescent Microscopy Image System, supplied by Evident Corporation, 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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Keygen Biotech integrated fluorescence microscopy imaging system bz-x800e
Silencing effects of pERK2 and caspase 3 with siRNA after excitotoxic SCI. (A, B, and C): Intrathecal pre-treatment for 72 h with ERK2 siRNA (B and C light bar, 2.5 μg) complexed with lipofectamine 2000 (5 μg) resulted in significant decrease in pERK2 protein expression 4 h after excitotoxic SCI, compared to control siRNA pretreatment (A and C dark bar, 2.5 μg). (D, E, and F): Intrathecal pre-treatment for 72 h with ERK2 siRNA (E and F light bar, 2.5 μg) complexed with lipofectamine 2000 (5 μg) resulted in significant decrease in caspase 3 activity (cleaved caspase 3) 4 h after excitotoxic SCI, compared to control siRNA pretreatment (D and F dark bar, 2.5 μg). The <t>fluorescent</t> labeled pERK2-positive or cleaved caspase 3-positive cells in the QUIS injection epicenter were counted using fliorescent <t>microscopy</t> <t>image</t> <t>system</t> (n=3 sections sparated 60 μm apart per animal, n=3 animals per group). Data were presented as mean ± S.E.M. and analyzed by t-test **p<0.01 and ***p<0.001, t test. Scale bar: 30 μm.
Integrated Fluorescence Microscopy Imaging System Bz X800e, supplied by Keygen Biotech, 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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Tecan Systems fluorescent microscopy image
Silencing effects of pERK2 and caspase 3 with siRNA after excitotoxic SCI. (A, B, and C): Intrathecal pre-treatment for 72 h with ERK2 siRNA (B and C light bar, 2.5 μg) complexed with lipofectamine 2000 (5 μg) resulted in significant decrease in pERK2 protein expression 4 h after excitotoxic SCI, compared to control siRNA pretreatment (A and C dark bar, 2.5 μg). (D, E, and F): Intrathecal pre-treatment for 72 h with ERK2 siRNA (E and F light bar, 2.5 μg) complexed with lipofectamine 2000 (5 μg) resulted in significant decrease in caspase 3 activity (cleaved caspase 3) 4 h after excitotoxic SCI, compared to control siRNA pretreatment (D and F dark bar, 2.5 μg). The <t>fluorescent</t> labeled pERK2-positive or cleaved caspase 3-positive cells in the QUIS injection epicenter were counted using fliorescent <t>microscopy</t> <t>image</t> <t>system</t> (n=3 sections sparated 60 μm apart per animal, n=3 animals per group). Data were presented as mean ± S.E.M. and analyzed by t-test **p<0.01 and ***p<0.001, t test. Scale bar: 30 μm.
Fluorescent Microscopy Image, supplied by Tecan Systems, 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/result/fluorescent microscopy image/product/Tecan Systems
Average 90 stars, based on 1 article reviews
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ImStar Therapeutics fluorescence microscopy imaging system imstar s.a
Silencing effects of pERK2 and caspase 3 with siRNA after excitotoxic SCI. (A, B, and C): Intrathecal pre-treatment for 72 h with ERK2 siRNA (B and C light bar, 2.5 μg) complexed with lipofectamine 2000 (5 μg) resulted in significant decrease in pERK2 protein expression 4 h after excitotoxic SCI, compared to control siRNA pretreatment (A and C dark bar, 2.5 μg). (D, E, and F): Intrathecal pre-treatment for 72 h with ERK2 siRNA (E and F light bar, 2.5 μg) complexed with lipofectamine 2000 (5 μg) resulted in significant decrease in caspase 3 activity (cleaved caspase 3) 4 h after excitotoxic SCI, compared to control siRNA pretreatment (D and F dark bar, 2.5 μg). The <t>fluorescent</t> labeled pERK2-positive or cleaved caspase 3-positive cells in the QUIS injection epicenter were counted using fliorescent <t>microscopy</t> <t>image</t> <t>system</t> (n=3 sections sparated 60 μm apart per animal, n=3 animals per group). Data were presented as mean ± S.E.M. and analyzed by t-test **p<0.01 and ***p<0.001, t test. Scale bar: 30 μm.
Fluorescence Microscopy Imaging System Imstar S.A, supplied by ImStar Therapeutics, 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/result/fluorescence microscopy imaging system imstar s.a/product/ImStar Therapeutics
Average 90 stars, based on 1 article reviews
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90
3DHistech ltd orth-fluorescent microscopy, imaging system, digital slide scanner
Silencing effects of pERK2 and caspase 3 with siRNA after excitotoxic SCI. (A, B, and C): Intrathecal pre-treatment for 72 h with ERK2 siRNA (B and C light bar, 2.5 μg) complexed with lipofectamine 2000 (5 μg) resulted in significant decrease in pERK2 protein expression 4 h after excitotoxic SCI, compared to control siRNA pretreatment (A and C dark bar, 2.5 μg). (D, E, and F): Intrathecal pre-treatment for 72 h with ERK2 siRNA (E and F light bar, 2.5 μg) complexed with lipofectamine 2000 (5 μg) resulted in significant decrease in caspase 3 activity (cleaved caspase 3) 4 h after excitotoxic SCI, compared to control siRNA pretreatment (D and F dark bar, 2.5 μg). The <t>fluorescent</t> labeled pERK2-positive or cleaved caspase 3-positive cells in the QUIS injection epicenter were counted using fliorescent <t>microscopy</t> <t>image</t> <t>system</t> (n=3 sections sparated 60 μm apart per animal, n=3 animals per group). Data were presented as mean ± S.E.M. and analyzed by t-test **p<0.01 and ***p<0.001, t test. Scale bar: 30 μm.
Orth Fluorescent Microscopy, Imaging System, Digital Slide Scanner, supplied by 3DHistech ltd, 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
scanalytics inc digital imaging fluorescence microscopy systems
Silencing effects of pERK2 and caspase 3 with siRNA after excitotoxic SCI. (A, B, and C): Intrathecal pre-treatment for 72 h with ERK2 siRNA (B and C light bar, 2.5 μg) complexed with lipofectamine 2000 (5 μg) resulted in significant decrease in pERK2 protein expression 4 h after excitotoxic SCI, compared to control siRNA pretreatment (A and C dark bar, 2.5 μg). (D, E, and F): Intrathecal pre-treatment for 72 h with ERK2 siRNA (E and F light bar, 2.5 μg) complexed with lipofectamine 2000 (5 μg) resulted in significant decrease in caspase 3 activity (cleaved caspase 3) 4 h after excitotoxic SCI, compared to control siRNA pretreatment (D and F dark bar, 2.5 μg). The <t>fluorescent</t> labeled pERK2-positive or cleaved caspase 3-positive cells in the QUIS injection epicenter were counted using fliorescent <t>microscopy</t> <t>image</t> <t>system</t> (n=3 sections sparated 60 μm apart per animal, n=3 animals per group). Data were presented as mean ± S.E.M. and analyzed by t-test **p<0.01 and ***p<0.001, t test. Scale bar: 30 μm.
Digital Imaging Fluorescence Microscopy Systems, supplied by scanalytics inc, 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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Applied Precision Inc deconvolution fluorescence microscopy with an applied precision deltavisiontm image restoration system
Silencing effects of pERK2 and caspase 3 with siRNA after excitotoxic SCI. (A, B, and C): Intrathecal pre-treatment for 72 h with ERK2 siRNA (B and C light bar, 2.5 μg) complexed with lipofectamine 2000 (5 μg) resulted in significant decrease in pERK2 protein expression 4 h after excitotoxic SCI, compared to control siRNA pretreatment (A and C dark bar, 2.5 μg). (D, E, and F): Intrathecal pre-treatment for 72 h with ERK2 siRNA (E and F light bar, 2.5 μg) complexed with lipofectamine 2000 (5 μg) resulted in significant decrease in caspase 3 activity (cleaved caspase 3) 4 h after excitotoxic SCI, compared to control siRNA pretreatment (D and F dark bar, 2.5 μg). The <t>fluorescent</t> labeled pERK2-positive or cleaved caspase 3-positive cells in the QUIS injection epicenter were counted using fliorescent <t>microscopy</t> <t>image</t> <t>system</t> (n=3 sections sparated 60 μm apart per animal, n=3 animals per group). Data were presented as mean ± S.E.M. and analyzed by t-test **p<0.01 and ***p<0.001, t test. Scale bar: 30 μm.
Deconvolution Fluorescence Microscopy With An Applied Precision Deltavisiontm Image Restoration System, supplied by Applied Precision Inc, 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


Silencing effects of pERK2 and caspase 3 with siRNA after excitotoxic SCI. (A, B, and C): Intrathecal pre-treatment for 72 h with ERK2 siRNA (B and C light bar, 2.5 μg) complexed with lipofectamine 2000 (5 μg) resulted in significant decrease in pERK2 protein expression 4 h after excitotoxic SCI, compared to control siRNA pretreatment (A and C dark bar, 2.5 μg). (D, E, and F): Intrathecal pre-treatment for 72 h with ERK2 siRNA (E and F light bar, 2.5 μg) complexed with lipofectamine 2000 (5 μg) resulted in significant decrease in caspase 3 activity (cleaved caspase 3) 4 h after excitotoxic SCI, compared to control siRNA pretreatment (D and F dark bar, 2.5 μg). The fluorescent labeled pERK2-positive or cleaved caspase 3-positive cells in the QUIS injection epicenter were counted using fliorescent microscopy image system (n=3 sections sparated 60 μm apart per animal, n=3 animals per group). Data were presented as mean ± S.E.M. and analyzed by t-test **p<0.01 and ***p<0.001, t test. Scale bar: 30 μm.

Journal: Journal of neurochemistry

Article Title: Involvement of ERK2 in traumatic spinal cord injury

doi: 10.1111/j.1471-4159.2010.06579.x

Figure Lengend Snippet: Silencing effects of pERK2 and caspase 3 with siRNA after excitotoxic SCI. (A, B, and C): Intrathecal pre-treatment for 72 h with ERK2 siRNA (B and C light bar, 2.5 μg) complexed with lipofectamine 2000 (5 μg) resulted in significant decrease in pERK2 protein expression 4 h after excitotoxic SCI, compared to control siRNA pretreatment (A and C dark bar, 2.5 μg). (D, E, and F): Intrathecal pre-treatment for 72 h with ERK2 siRNA (E and F light bar, 2.5 μg) complexed with lipofectamine 2000 (5 μg) resulted in significant decrease in caspase 3 activity (cleaved caspase 3) 4 h after excitotoxic SCI, compared to control siRNA pretreatment (D and F dark bar, 2.5 μg). The fluorescent labeled pERK2-positive or cleaved caspase 3-positive cells in the QUIS injection epicenter were counted using fliorescent microscopy image system (n=3 sections sparated 60 μm apart per animal, n=3 animals per group). Data were presented as mean ± S.E.M. and analyzed by t-test **p<0.01 and ***p<0.001, t test. Scale bar: 30 μm.

Article Snippet: The fluorescent ERK2 or ED-1signal in the lentiviral vector injection epicenter were imaged/analyzed and the pERK2-positive or cleaved caspase 3-positive cells in the QUIS lesion epicenter were counted using an Olympus spinning disk fluorescent microscopy image system and Adobe Photoshop CS2 software (n=3 sections separated 60 μm apart per animal, n= 3-4 animals per group).

Techniques: Expressing, Activity Assay, Labeling, Injection, Microscopy