axio observer z1 inverted wide field microscope (Carl Zeiss)
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Carl Zeiss
axio observer z1 inverted wide field microscope
Axio Observer Z1 Inverted Wide Field Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 99/100, based on 4874 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/field+axio+observer+z1/Inverted+microscope+Axio+Observer+3/bio_rxiv__64898__2026__02__02__703230-176-9-8
Average 99 stars, based on 4874 article reviews
Axio Observer Z1 Inverted Wide Field Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 99/100, based on 4874 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/field+axio+observer+z1/Inverted+microscope+Axio+Observer+3/bio_rxiv__64898__2026__02__02__703230-176-9-8
Average 99 stars, based on 4874 article reviews
axio observer z1 inverted wide field microscope - by Bioz Stars,
2026-10
99/100 stars
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Software:Article Title: Optogenetic Control of Phosphate-Responsive Genes Using Single-Component Fusion Proteins in Saccharomyces cerevisiae . Article Snippet: Blue light illumination can be detected by lightoxygen-voltage (LOV) photosensing proteins and translated into a range of biochemical responses, facilitating the generation of novel optogenetic tools to control cellular function.. Here, we develop new variants of our previously described VP-EL222 lightdependent transcription factor and apply them to study the phosphate-responsive signaling (PHO) pathway in the budding yeast Saccharomyces cerevisiae, exemplifying the utilities of these new tools.. Focusing first on the VP-EL222 protein itself, we quantified the tunability of gene expression as a function of light intensity and duration and demonstrated that this system can tolerate the addition of substantially larger effector domains without impacting function. Article Title: Optogenetic control of phosphate-responsive genes using single component fusion proteins in Saccharomyces cerevisiae Article Snippet: For flow cytometry, samples were analyzed using a BD Accuri C6 Sampler Plus flow cytometer, light plate first, followed by unwrapping of the dark plate. .. Data was then processed using FlowJo software 61 . mCherry fluorescence was observed using either a Article Title: Optogenetic control of phosphate-responsive genes using single component fusion proteins in Saccharomyces cerevisiae Article Snippet: .. Data was then processed using FlowJo software . mCherry fluorescence was observed using either a Fluorescence:Article Title: Optogenetic Control of Phosphate-Responsive Genes Using Single-Component Fusion Proteins in Saccharomyces cerevisiae . Article Snippet: Blue light illumination can be detected by lightoxygen-voltage (LOV) photosensing proteins and translated into a range of biochemical responses, facilitating the generation of novel optogenetic tools to control cellular function.. Here, we develop new variants of our previously described VP-EL222 lightdependent transcription factor and apply them to study the phosphate-responsive signaling (PHO) pathway in the budding yeast Saccharomyces cerevisiae, exemplifying the utilities of these new tools.. Focusing first on the VP-EL222 protein itself, we quantified the tunability of gene expression as a function of light intensity and duration and demonstrated that this system can tolerate the addition of substantially larger effector domains without impacting function. Article Title: Optogenetic control of phosphate-responsive genes using single component fusion proteins in Saccharomyces cerevisiae Article Snippet: For flow cytometry, samples were analyzed using a BD Accuri C6 Sampler Plus flow cytometer, light plate first, followed by unwrapping of the dark plate. .. Data was then processed using FlowJo software 61 . mCherry fluorescence was observed using either a Article Title: Optogenetic control of phosphate-responsive genes using single component fusion proteins in Saccharomyces cerevisiae Article Snippet: .. Data was then processed using FlowJo software . mCherry fluorescence was observed using either a Inverted Microscopy:Article Title: Optogenetic Control of Phosphate-Responsive Genes Using Single-Component Fusion Proteins in Saccharomyces cerevisiae . Article Snippet: Blue light illumination can be detected by lightoxygen-voltage (LOV) photosensing proteins and translated into a range of biochemical responses, facilitating the generation of novel optogenetic tools to control cellular function.. Here, we develop new variants of our previously described VP-EL222 lightdependent transcription factor and apply them to study the phosphate-responsive signaling (PHO) pathway in the budding yeast Saccharomyces cerevisiae, exemplifying the utilities of these new tools.. Focusing first on the VP-EL222 protein itself, we quantified the tunability of gene expression as a function of light intensity and duration and demonstrated that this system can tolerate the addition of substantially larger effector domains without impacting function. Article Title: Optogenetic control of phosphate-responsive genes using single component fusion proteins in Saccharomyces cerevisiae Article Snippet: For flow cytometry, samples were analyzed using a BD Accuri C6 Sampler Plus flow cytometer, light plate first, followed by unwrapping of the dark plate. .. Data was then processed using FlowJo software 61 . mCherry fluorescence was observed using either a Article Title: Optogenetic control of phosphate-responsive genes using single component fusion proteins in Saccharomyces cerevisiae Article Snippet: .. Data was then processed using FlowJo software . mCherry fluorescence was observed using either a Microscopy:Article Title: Optogenetic Control of Phosphate-Responsive Genes Using Single-Component Fusion Proteins in Saccharomyces cerevisiae . Article Snippet: Blue light illumination can be detected by lightoxygen-voltage (LOV) photosensing proteins and translated into a range of biochemical responses, facilitating the generation of novel optogenetic tools to control cellular function.. Here, we develop new variants of our previously described VP-EL222 lightdependent transcription factor and apply them to study the phosphate-responsive signaling (PHO) pathway in the budding yeast Saccharomyces cerevisiae, exemplifying the utilities of these new tools.. Focusing first on the VP-EL222 protein itself, we quantified the tunability of gene expression as a function of light intensity and duration and demonstrated that this system can tolerate the addition of substantially larger effector domains without impacting function. Article Title: Optogenetic control of phosphate-responsive genes using single component fusion proteins in Saccharomyces cerevisiae Article Snippet: For flow cytometry, samples were analyzed using a BD Accuri C6 Sampler Plus flow cytometer, light plate first, followed by unwrapping of the dark plate. .. Data was then processed using FlowJo software 61 . mCherry fluorescence was observed using either a Article Title: Optogenetic control of phosphate-responsive genes using single component fusion proteins in Saccharomyces cerevisiae Article Snippet: .. Data was then processed using FlowJo software . mCherry fluorescence was observed using either a |