Log In Sign up
The largest database of trusted experimental protocols

Lsm software

Manufactured by Adobe
Visit Supplier

The LSM software is a core component of Adobe's laboratory equipment offerings. It is designed to provide users with a comprehensive tool for analyzing and manipulating digital images and data. The software offers a range of functionalities, including image processing, visualization, and data analysis, catering to the needs of researchers and scientists working in various fields.

Automatically generated - may contain errors

Lab products found in correlation

Xm10 digital camera, by Olympus (2 mentions) Bx51 fluorescence microscope, by Olympus (2 mentions) Laser scanning microscope 510, by Zeiss (2 mentions) 510 meta confocal microscope, by Zeiss (1 mentions)

Spelling variants of this product

LSM 5 Image Browser software (4 citations) LSM Image Browser software (3 citations)

3 protocols using lsm software

1

Confocal Microscopy Imaging Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
A Zeiss META 510 confocal microscope was used to collect data for all fluorescent images; confocal stacks were merged using Zeiss LSM software or Adobe Photoshop CS4. Where appropriate, images were false-colored to assist color-blind readers or to represent data more clearly.
Gabilondo H., Rubio-Ferrera I., Losada-Pérez M., del Saz D., León Y., Molina I., Torroja L., W. Allan D, & Benito-Sipos J. (2018). Segmentally homologous neurons acquire two different terminal neuropeptidergic fates in the Drosophila nervous system. PLoS ONE, 13(4), e0194281.
+ Open protocol
+ Expand
2

Fluorescence Microscopy Imaging Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
Photomicrographs were taken with an Olympus XM10 digital camera mounted on an Olympus BX51 fluorescence microscope (Olympus Sweden). Illustrations were prepared in Adobe Illustrator and Adobe Photoshop CS4. Images were only adjusted for brightness and contrast. Confocal Z-stacks of optical sections were obtained using a Zeiss Laser scanning microscope 510, and the projection images were processed using the Zeiss LSM software, ImageJ and Adobe Photoshop CS4.
Kardamakis A.A., Pérez-Fernández J, & Grillner S. (2016). Spatiotemporal interplay between multisensory excitation and recruited inhibition in the lamprey optic tectum. eLife, 5, e16472.
+ Open protocol
+ Expand
3

Fluorescence Microscopy Imaging Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
Photomicrographs were taken with an Olympus XM10 digital camera mounted on an Olympus BX51 fluorescence microscope (Olympus Sweden). Illustrations were prepared in Adobe Illustrator and Adobe Photoshop CS4. Images were only adjusted for brightness and contrast. Confocal Z stacks of optical sections were obtained using a Zeiss Laser scanning microscope 510, and the projection images were processed using the Zeiss LSM software, ImageJ and Adobe Photoshop CS4.
Pérez-Fernández J., Kardamakis A.A., Suzuki D.G., Robertson B, & Grillner S. (2017). Direct Dopaminergic Projections from the SNc Modulate Visuomotor Transformation in the Lamprey Tectum. Neuron, 96(4).
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!