confocal laser scanning microscope clsm bio rad mrc 600 (Bio-Rad)
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confocal laser scanning microscope clsm bio rad mrc 600
Confocal Laser Scanning Microscope Clsm Bio Rad Mrc 600, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/bio+rad+mrc+600+clsm/Lyphochek+Hypertension+Markers+Control/10__1515_slash_bjdm___2015___0033-39-13-18
Average 97 stars, based on 1 article reviews
Confocal Laser Scanning Microscope Clsm Bio Rad Mrc 600, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/bio+rad+mrc+600+clsm/Lyphochek+Hypertension+Markers+Control/10__1515_slash_bjdm___2015___0033-39-13-18
Average 97 stars, based on 1 article reviews
confocal laser scanning microscope clsm bio rad mrc 600 - by Bioz Stars,
2026-09
97/100 stars
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Confocal Laser Scanning Microscopy:Article Title: Dual modes of rabies P-protein association with microtubules: a novel strategy to suppress the antiviral response. Article Snippet: For indirect immunofluorescence of STAT1, cells were washed with PBS before fixation with 3.7% formaldehyde in PBS (10 minutes at room temperature) followed by 90% methanol (5 minutes at room temperature) before blocking (1% BSA, 2 hours, room temperature) and staining with anti-STAT1 (BD Biosciences, 610185) or antiSTAT1-P (Santa Cruz Biotechnology, sc-7988) followed by Alexa-Fluor-568-coupled secondary antibody (Invitrogen). .. Confocal laser-scanning microscopy and image analysis Routine CLSM for single-colour fluorophore live-cell analysis was performed using a Article Title: Apoptin Nuclear Accumulation Is Modulated by a CRM1-Recognized Nuclear Export Signal that Is Active in Normal but not in Tumor Cells Article Snippet: .. Cells were imaged by confocal laser scanning microscopy (CLSM) using Article Title: Dynein Light Chain Association Sequences Can Facilitate Nuclear Protein Import Article Snippet: Imaging of live cells was performed using a Bio-Rad MRC-600 CLSM (Richmond, CA) with a 40× water immersion objective and heated stage ( Lam et al. , 2002 ; Alvisi et al. , 2005 ; Poon et al. , 2005 ) or, for high-magnification images, an Olympus Fluoview 1000 with a 100× oil immersion objective and heated stage (Melville, NY; Roth et al. , 2007 ). .. Fixed cells were viewed on a Article Title: Dynein Light Chain Association Sequences Can Facilitate Nuclear Protein Import Article Snippet: For stabilization of the MT cytoskeleton, taxol was added to a final concentration of 1 μg/ml for 4 h as described previously ( Roth et al. , 2007 ). .. CLSM and Image Analysis Imaging of live cells was performed using a Article Title: Nucleocytoplasmic distribution of rabies virus P-protein is regulated by phosphorylation adjacent to C-terminal nuclear import and export signals. Article Snippet: Nucleocytoplasmic distribution of the rabies virus phosphoprotein is implicated in the evasion of cellular antiviral mechanisms by rabies virus and has been reported to depend on an N-terminal nuclear export sequence and a C-terminal nuclear localization sequence.. This paper identifies a second nuclear export sequence that is located between key residues of the nuclear localization sequence in the phosphoprotein C-terminal domain.. The C-terminal domain confers predominantly nuclear localization in unstimulated transfected cells, indicating that the nuclear localization sequence is the dominant signal at steady state. Article Title: Dynein Light Chain Association Sequences Can Facilitate Nuclear Protein Import Article Snippet: For stabilization of the MT cytoskeleton, taxol was added to a final concentration of 1 μg/ml for 4 h as described previously ( Roth et al. , 2007 ). .. Imaging of live cells was performed using a Article Title: Proceedings of scanning 98 Baltimore, Maryland, USA Article Snippet: .. Observations were made in a slow scan confocal microscope, the Imaging:Article Title: Dual modes of rabies P-protein association with microtubules: a novel strategy to suppress the antiviral response. Article Snippet: For indirect immunofluorescence of STAT1, cells were washed with PBS before fixation with 3.7% formaldehyde in PBS (10 minutes at room temperature) followed by 90% methanol (5 minutes at room temperature) before blocking (1% BSA, 2 hours, room temperature) and staining with anti-STAT1 (BD Biosciences, 610185) or antiSTAT1-P (Santa Cruz Biotechnology, sc-7988) followed by Alexa-Fluor-568-coupled secondary antibody (Invitrogen). .. Confocal laser-scanning microscopy and image analysis Routine CLSM for single-colour fluorophore live-cell analysis was performed using a Article Title: Dynein Light Chain Association Sequences Can Facilitate Nuclear Protein Import Article Snippet: For stabilization of the MT cytoskeleton, taxol was added to a final concentration of 1 μg/ml for 4 h as described previously ( Roth et al. , 2007 ). .. CLSM and Image Analysis Imaging of live cells was performed using a Article Title: Nucleocytoplasmic distribution of rabies virus P-protein is regulated by phosphorylation adjacent to C-terminal nuclear import and export signals. Article Snippet: Nucleocytoplasmic distribution of the rabies virus phosphoprotein is implicated in the evasion of cellular antiviral mechanisms by rabies virus and has been reported to depend on an N-terminal nuclear export sequence and a C-terminal nuclear localization sequence.. This paper identifies a second nuclear export sequence that is located between key residues of the nuclear localization sequence in the phosphoprotein C-terminal domain.. The C-terminal domain confers predominantly nuclear localization in unstimulated transfected cells, indicating that the nuclear localization sequence is the dominant signal at steady state. Article Title: Dynein Light Chain Association Sequences Can Facilitate Nuclear Protein Import Article Snippet: For stabilization of the MT cytoskeleton, taxol was added to a final concentration of 1 μg/ml for 4 h as described previously ( Roth et al. , 2007 ). .. Imaging of live cells was performed using a Live Cell Imaging:Article Title: Dual modes of rabies P-protein association with microtubules: a novel strategy to suppress the antiviral response. Article Snippet: For indirect immunofluorescence of STAT1, cells were washed with PBS before fixation with 3.7% formaldehyde in PBS (10 minutes at room temperature) followed by 90% methanol (5 minutes at room temperature) before blocking (1% BSA, 2 hours, room temperature) and staining with anti-STAT1 (BD Biosciences, 610185) or antiSTAT1-P (Santa Cruz Biotechnology, sc-7988) followed by Alexa-Fluor-568-coupled secondary antibody (Invitrogen). .. Confocal laser-scanning microscopy and image analysis Routine CLSM for single-colour fluorophore live-cell analysis was performed using a Microscopy:Article Title: Proceedings of scanning 98 Baltimore, Maryland, USA Article Snippet: .. Observations were made in a slow scan confocal microscope, the |