image scope analytical computer software Search Results


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Bioimager Inc scope image 9.0 software
Scope Image 9.0 Software, supplied by Bioimager 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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Lab Scope Video Software Gti 2000 Real Time Image Workstation Ver1.30.0, supplied by Glenbrook Technologies 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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BP Integrated Technologies Inc scope image 9.0 professional imaging software
Scope Image 9.0 Professional Imaging Software, supplied by BP Integrated Technologies 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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Hamamatsu imageem emccd camera
Imageem Emccd 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
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Nikon 80i upright research fluorescence scope
FIGURE 6. N91Q and N612Q ADAM8 mutants are unable to reach the cell surface. A, SUM-149 cells were transiently transfected with vectors express- ing WT ADAM8 or N67Q, N91Q, N436Q, or N612Q N-glycosylation mutants. Cells were fixed, permeabilized, and subjected to immunofluorescent stain- ing for ADAM8 expression using an anti-ADAM8 ectodomain antibody (AF1031) (red), and for the cell surface marker E-cadherin (green), and with DAPI (blue) to label the nuclei. Images were taken using a Nikon <t>80i</t> Upright Research <t>Fluorescence</t> Scope (40 objective) with an Andoe Clara-E Camera andprocessedwithNIS-ElementsBasicsoftware.Scalebar,10m.B,HEK-293 cells were transiently transfected with vectors expressing WT ADAM8 or N-glycosylation mutants N91Q and N612Q. The cell surface proteins were labeled with biotin and pulled down by streptavidin (SA)-conjugated beads. Samples (10%) of extracts (Input) and pulled down biotinylated ADAM8 were detected by Western blotting using a Myc antibody.
80i Upright Research Fluorescence Scope, 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/image+scope+analytical+computer+software/Objectives/10__1074_slash_jbc__m114__594242-97-6-5
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80i upright research fluorescence scope - by Bioz Stars, 2026-08
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Nikon nikon c2 confocal scope
FIGURE 6. N91Q and N612Q ADAM8 mutants are unable to reach the cell surface. A, SUM-149 cells were transiently transfected with vectors express- ing WT ADAM8 or N67Q, N91Q, N436Q, or N612Q N-glycosylation mutants. Cells were fixed, permeabilized, and subjected to immunofluorescent stain- ing for ADAM8 expression using an anti-ADAM8 ectodomain antibody (AF1031) (red), and for the cell surface marker E-cadherin (green), and with DAPI (blue) to label the nuclei. Images were taken using a Nikon <t>80i</t> Upright Research <t>Fluorescence</t> Scope (40 objective) with an Andoe Clara-E Camera andprocessedwithNIS-ElementsBasicsoftware.Scalebar,10m.B,HEK-293 cells were transiently transfected with vectors expressing WT ADAM8 or N-glycosylation mutants N91Q and N612Q. The cell surface proteins were labeled with biotin and pulled down by streptavidin (SA)-conjugated beads. Samples (10%) of extracts (Input) and pulled down biotinylated ADAM8 were detected by Western blotting using a Myc antibody.
Nikon C2 Confocal Scope, 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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BIOSCAN INC image analysis software invivo scope
FIGURE 6. N91Q and N612Q ADAM8 mutants are unable to reach the cell surface. A, SUM-149 cells were transiently transfected with vectors express- ing WT ADAM8 or N67Q, N91Q, N436Q, or N612Q N-glycosylation mutants. Cells were fixed, permeabilized, and subjected to immunofluorescent stain- ing for ADAM8 expression using an anti-ADAM8 ectodomain antibody (AF1031) (red), and for the cell surface marker E-cadherin (green), and with DAPI (blue) to label the nuclei. Images were taken using a Nikon <t>80i</t> Upright Research <t>Fluorescence</t> Scope (40 objective) with an Andoe Clara-E Camera andprocessedwithNIS-ElementsBasicsoftware.Scalebar,10m.B,HEK-293 cells were transiently transfected with vectors expressing WT ADAM8 or N-glycosylation mutants N91Q and N612Q. The cell surface proteins were labeled with biotin and pulled down by streptavidin (SA)-conjugated beads. Samples (10%) of extracts (Input) and pulled down biotinylated ADAM8 were detected by Western blotting using a Myc antibody.
Image Analysis Software Invivo Scope, supplied by BIOSCAN 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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ACCU-SCOPE inc captavision
FIGURE 6. N91Q and N612Q ADAM8 mutants are unable to reach the cell surface. A, SUM-149 cells were transiently transfected with vectors express- ing WT ADAM8 or N67Q, N91Q, N436Q, or N612Q N-glycosylation mutants. Cells were fixed, permeabilized, and subjected to immunofluorescent stain- ing for ADAM8 expression using an anti-ADAM8 ectodomain antibody (AF1031) (red), and for the cell surface marker E-cadherin (green), and with DAPI (blue) to label the nuclei. Images were taken using a Nikon <t>80i</t> Upright Research <t>Fluorescence</t> Scope (40 objective) with an Andoe Clara-E Camera andprocessedwithNIS-ElementsBasicsoftware.Scalebar,10m.B,HEK-293 cells were transiently transfected with vectors expressing WT ADAM8 or N-glycosylation mutants N91Q and N612Q. The cell surface proteins were labeled with biotin and pulled down by streptavidin (SA)-conjugated beads. Samples (10%) of extracts (Input) and pulled down biotinylated ADAM8 were detected by Western blotting using a Myc antibody.
Captavision, supplied by ACCU-SCOPE 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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ACCU-SCOPE inc micrometric se premium software
FIGURE 6. N91Q and N612Q ADAM8 mutants are unable to reach the cell surface. A, SUM-149 cells were transiently transfected with vectors express- ing WT ADAM8 or N67Q, N91Q, N436Q, or N612Q N-glycosylation mutants. Cells were fixed, permeabilized, and subjected to immunofluorescent stain- ing for ADAM8 expression using an anti-ADAM8 ectodomain antibody (AF1031) (red), and for the cell surface marker E-cadherin (green), and with DAPI (blue) to label the nuclei. Images were taken using a Nikon <t>80i</t> Upright Research <t>Fluorescence</t> Scope (40 objective) with an Andoe Clara-E Camera andprocessedwithNIS-ElementsBasicsoftware.Scalebar,10m.B,HEK-293 cells were transiently transfected with vectors expressing WT ADAM8 or N-glycosylation mutants N91Q and N612Q. The cell surface proteins were labeled with biotin and pulled down by streptavidin (SA)-conjugated beads. Samples (10%) of extracts (Input) and pulled down biotinylated ADAM8 were detected by Western blotting using a Myc antibody.
Micrometric Se Premium Software, supplied by ACCU-SCOPE 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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Nikon nikon ds ri2 scope
FIGURE 6. N91Q and N612Q ADAM8 mutants are unable to reach the cell surface. A, SUM-149 cells were transiently transfected with vectors express- ing WT ADAM8 or N67Q, N91Q, N436Q, or N612Q N-glycosylation mutants. Cells were fixed, permeabilized, and subjected to immunofluorescent stain- ing for ADAM8 expression using an anti-ADAM8 ectodomain antibody (AF1031) (red), and for the cell surface marker E-cadherin (green), and with DAPI (blue) to label the nuclei. Images were taken using a Nikon <t>80i</t> Upright Research <t>Fluorescence</t> Scope (40 objective) with an Andoe Clara-E Camera andprocessedwithNIS-ElementsBasicsoftware.Scalebar,10m.B,HEK-293 cells were transiently transfected with vectors expressing WT ADAM8 or N-glycosylation mutants N91Q and N612Q. The cell surface proteins were labeled with biotin and pulled down by streptavidin (SA)-conjugated beads. Samples (10%) of extracts (Input) and pulled down biotinylated ADAM8 were detected by Western blotting using a Myc antibody.
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Nikon fluorescent micro scope
FIGURE 6. N91Q and N612Q ADAM8 mutants are unable to reach the cell surface. A, SUM-149 cells were transiently transfected with vectors express- ing WT ADAM8 or N67Q, N91Q, N436Q, or N612Q N-glycosylation mutants. Cells were fixed, permeabilized, and subjected to immunofluorescent stain- ing for ADAM8 expression using an anti-ADAM8 ectodomain antibody (AF1031) (red), and for the cell surface marker E-cadherin (green), and with DAPI (blue) to label the nuclei. Images were taken using a Nikon <t>80i</t> Upright Research <t>Fluorescence</t> Scope (40 objective) with an Andoe Clara-E Camera andprocessedwithNIS-ElementsBasicsoftware.Scalebar,10m.B,HEK-293 cells were transiently transfected with vectors expressing WT ADAM8 or N-glycosylation mutants N91Q and N612Q. The cell surface proteins were labeled with biotin and pulled down by streptavidin (SA)-conjugated beads. Samples (10%) of extracts (Input) and pulled down biotinylated ADAM8 were detected by Western blotting using a Myc antibody.
Fluorescent Micro Scope, 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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Image Search Results


FIGURE 6. N91Q and N612Q ADAM8 mutants are unable to reach the cell surface. A, SUM-149 cells were transiently transfected with vectors express- ing WT ADAM8 or N67Q, N91Q, N436Q, or N612Q N-glycosylation mutants. Cells were fixed, permeabilized, and subjected to immunofluorescent stain- ing for ADAM8 expression using an anti-ADAM8 ectodomain antibody (AF1031) (red), and for the cell surface marker E-cadherin (green), and with DAPI (blue) to label the nuclei. Images were taken using a Nikon 80i Upright Research Fluorescence Scope (40 objective) with an Andoe Clara-E Camera andprocessedwithNIS-ElementsBasicsoftware.Scalebar,10m.B,HEK-293 cells were transiently transfected with vectors expressing WT ADAM8 or N-glycosylation mutants N91Q and N612Q. The cell surface proteins were labeled with biotin and pulled down by streptavidin (SA)-conjugated beads. Samples (10%) of extracts (Input) and pulled down biotinylated ADAM8 were detected by Western blotting using a Myc antibody.

Journal: Journal of Biological Chemistry

Article Title: N-Glycosylation Regulates ADAM8 Processing and Activation

doi: 10.1074/jbc.m114.594242

Figure Lengend Snippet: FIGURE 6. N91Q and N612Q ADAM8 mutants are unable to reach the cell surface. A, SUM-149 cells were transiently transfected with vectors express- ing WT ADAM8 or N67Q, N91Q, N436Q, or N612Q N-glycosylation mutants. Cells were fixed, permeabilized, and subjected to immunofluorescent stain- ing for ADAM8 expression using an anti-ADAM8 ectodomain antibody (AF1031) (red), and for the cell surface marker E-cadherin (green), and with DAPI (blue) to label the nuclei. Images were taken using a Nikon 80i Upright Research Fluorescence Scope (40 objective) with an Andoe Clara-E Camera andprocessedwithNIS-ElementsBasicsoftware.Scalebar,10m.B,HEK-293 cells were transiently transfected with vectors expressing WT ADAM8 or N-glycosylation mutants N91Q and N612Q. The cell surface proteins were labeled with biotin and pulled down by streptavidin (SA)-conjugated beads. Samples (10%) of extracts (Input) and pulled down biotinylated ADAM8 were detected by Western blotting using a Myc antibody.

Article Snippet: Images were taken using a Nikon 80i Upright Research Fluorescence Scope (40x objective) with Andoe Clara-E Camera and processed with NIS-Elements Basic software.

Techniques: Transfection, Glycoproteomics, Staining, Expressing, Marker, Fluorescence, Labeling, Western Blot