Our new Obvious+ tissue clearing system is the only technique that delipidates samples without any modify in morphology and with negligible effect on structural integrity.
Our transform-key SmartBatch+ program combines electrophoretic tissue clearing and immunolabeling into just one large-throughput unit.
Request a estimate or demo Uniformly section large tissues & sample arrays Megatome is the only microtome that may segment samples as huge as intact nonhuman primate and human organs, which makes it priceless for fields including neuropathology.
Operating the CLI directly from a Gradle task is not now supported. A distribution needs to be established by means of gradlew :j2d-cli:distZip to produce a zip file made up of everything needed to run.
Clone the project or grab the most up-to-date launch. Operating the utility will vary somewhat according to how you retrieve the challenge.
Our preformulated EasyIndex Alternative raises and homogenize the refractive index of delipidated tissue samples, rendering them completely clear. This enables mild penetration in the sample and makes sure the acquisition of higher-resolution, in-concentration picture data.
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eFLASH is a rapid tissue labeling method that allows for uniform whole-organ staining in 20 rounds of labeling.
The SmartSPIM gentle sheet microscope supplies unparalleled resolution and acquisition pace during intact tissue volumes, although its modular design and style permits you to enhance and customize person components.
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Defend avoids the megatomi.com variability of hydrogel embedding and the knowledge loss from PFA preservation, guarding specimens for a number of rounds of processing.
Leverage the Clear+ tissue clearing technique, as well as eFLASH and patented stochastic electrotransport systems, to fast clear and label entire organs. Essential highlights and capabilities involve:
Our novel SHIELD tissue preservation procedure sorts intramolecular bonds working with polyfunctional, adaptable epoxides to stabilize tissue architecture and safeguard the sample’s endogenous fluorescence, protein antigenicity and nucleic acids.
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