ti e inverted fluorescence wide field microscope (Nikon)
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ti e inverted fluorescence wide field microscope
Ti E Inverted Fluorescence Wide Field Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 59743 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ti+e+inverted+wide+field+fluorescence+microscope/Objectives/10__1038_slash_s42005___025___02392___8-265-9-8
Average 99 stars, based on 59743 article reviews
Ti E Inverted Fluorescence Wide Field Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 59743 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ti+e+inverted+wide+field+fluorescence+microscope/Objectives/10__1038_slash_s42005___025___02392___8-265-9-8
Average 99 stars, based on 59743 article reviews
ti e inverted fluorescence wide field microscope - by Bioz Stars,
2026-09
99/100 stars
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Fluorescence:Article Title: Improved yellow-green split fluorescent proteins for protein labeling and signal amplification Article Snippet: After 48 hours, cells were fixed with 4% paraformaldehyde (diluted from 16% paraformaldehyde aqueous solution, Electron Microscopy Sciences) for 15 min and washed with PBS for three times. .. Then cells were imaged on a Nikon Article Title: Cross-membrane cooperation among bacteria can facilitate intracellular pathogenesis Article Snippet: Cover slips were then mounted on glass slides using ProLong Diamond Antifade mountant (Thermo Fisher Scientific). .. Samples were cured over night at room temperature and then imaged using a Nikon Article Title: Cross-membrane cooperation among bacteria can facilitate intracellular pathogenesis Article Snippet: .. Images were acquired using a Nikon Article Title: Improved split fluorescent proteins for endogenous protein labeling Article Snippet: Most of live-cell imaging was acquired on an inverted Nikon Ti-E microscope (UCSF Nikon Imaging Center), a Yokogawa CSU-W1 confocal scanner unit, a PlanApo VC 100x/1.4NA oil immersion objective, a stage incubator, an Andor Zyla 4.2 sCMOS or an Andor iXon Ultra DU888 EMCCD camera and MicroManager software. .. PAsfCherry2 photoactivation in H2B labeling and split mNG2 vs. split GFP comparison in H2B labeling were imaged on a Nikon Article Title: Bright split red fluorescent proteins with enhanced complementation efficiency for the tagging of endogenous proteins and visualization of synapses Article Snippet: .. 48 hours after transfection, cells were fixed with 4% paraformaldehyde and then imaged on a Nikon Article Title: Improved yellow-green split fluorescent proteins for protein labeling and signal amplification Article Snippet: After 48 hours, cells were fixed with 4% paraformaldehyde (diluted from 16% paraformaldehyde aqueous solution, Electron Microscopy Sciences) for 15 min and washed with PBS for three times. .. Then cells were imaged on a Nikon Article Title: Efficient labeling and imaging of protein-coding genes in living cells using CRISPR-Tag Article Snippet: .. CRISPR imaging data were acquired on a Nikon Article Title: CRISPR-Tag: an Efficient DNA Tagging System in Living Cells Article Snippet: .. CRISPR imaging data were acquired on a Nikon Microscopy:Article Title: Improved yellow-green split fluorescent proteins for protein labeling and signal amplification Article Snippet: After 48 hours, cells were fixed with 4% paraformaldehyde (diluted from 16% paraformaldehyde aqueous solution, Electron Microscopy Sciences) for 15 min and washed with PBS for three times. .. Then cells were imaged on a Nikon Article Title: Cross-membrane cooperation among bacteria can facilitate intracellular pathogenesis Article Snippet: Cover slips were then mounted on glass slides using ProLong Diamond Antifade mountant (Thermo Fisher Scientific). .. Samples were cured over night at room temperature and then imaged using a Nikon Article Title: Cross-membrane cooperation among bacteria can facilitate intracellular pathogenesis Article Snippet: .. Images were acquired using a Nikon Article Title: Improved split fluorescent proteins for endogenous protein labeling Article Snippet: Most of live-cell imaging was acquired on an inverted Nikon Ti-E microscope (UCSF Nikon Imaging Center), a Yokogawa CSU-W1 confocal scanner unit, a PlanApo VC 100x/1.4NA oil immersion objective, a stage incubator, an Andor Zyla 4.2 sCMOS or an Andor iXon Ultra DU888 EMCCD camera and MicroManager software. .. PAsfCherry2 photoactivation in H2B labeling and split mNG2 vs. split GFP comparison in H2B labeling were imaged on a Nikon Article Title: Bright split red fluorescent proteins with enhanced complementation efficiency for the tagging of endogenous proteins and visualization of synapses Article Snippet: .. 48 hours after transfection, cells were fixed with 4% paraformaldehyde and then imaged on a Nikon Article Title: Improved yellow-green split fluorescent proteins for protein labeling and signal amplification Article Snippet: After 48 hours, cells were fixed with 4% paraformaldehyde (diluted from 16% paraformaldehyde aqueous solution, Electron Microscopy Sciences) for 15 min and washed with PBS for three times. .. Then cells were imaged on a Nikon Article Title: Efficient labeling and imaging of protein-coding genes in living cells using CRISPR-Tag Article Snippet: .. CRISPR imaging data were acquired on a Nikon Article Title: CRISPR-Tag: an Efficient DNA Tagging System in Living Cells Article Snippet: .. CRISPR imaging data were acquired on a Nikon Labeling:Article Title: Improved split fluorescent proteins for endogenous protein labeling Article Snippet: Most of live-cell imaging was acquired on an inverted Nikon Ti-E microscope (UCSF Nikon Imaging Center), a Yokogawa CSU-W1 confocal scanner unit, a PlanApo VC 100x/1.4NA oil immersion objective, a stage incubator, an Andor Zyla 4.2 sCMOS or an Andor iXon Ultra DU888 EMCCD camera and MicroManager software. .. PAsfCherry2 photoactivation in H2B labeling and split mNG2 vs. split GFP comparison in H2B labeling were imaged on a Nikon Comparison:Article Title: Improved split fluorescent proteins for endogenous protein labeling Article Snippet: Most of live-cell imaging was acquired on an inverted Nikon Ti-E microscope (UCSF Nikon Imaging Center), a Yokogawa CSU-W1 confocal scanner unit, a PlanApo VC 100x/1.4NA oil immersion objective, a stage incubator, an Andor Zyla 4.2 sCMOS or an Andor iXon Ultra DU888 EMCCD camera and MicroManager software. .. PAsfCherry2 photoactivation in H2B labeling and split mNG2 vs. split GFP comparison in H2B labeling were imaged on a Nikon Transfection:Article Title: Bright split red fluorescent proteins with enhanced complementation efficiency for the tagging of endogenous proteins and visualization of synapses Article Snippet: .. 48 hours after transfection, cells were fixed with 4% paraformaldehyde and then imaged on a Nikon CRISPR:Article Title: Efficient labeling and imaging of protein-coding genes in living cells using CRISPR-Tag Article Snippet: .. CRISPR imaging data were acquired on a Nikon Article Title: CRISPR-Tag: an Efficient DNA Tagging System in Living Cells Article Snippet: .. CRISPR imaging data were acquired on a Nikon Imaging:Article Title: Efficient labeling and imaging of protein-coding genes in living cells using CRISPR-Tag Article Snippet: .. CRISPR imaging data were acquired on a Nikon Article Title: CRISPR-Tag: an Efficient DNA Tagging System in Living Cells Article Snippet: .. CRISPR imaging data were acquired on a Nikon |