Our new Very clear+ tissue clearing method is the only process that delipidates samples without adjust in morphology and with minimum influence on structural integrity.
Our transform-key SmartBatch+ method combines electrophoretic tissue clearing and immunolabeling into a single substantial-throughput system.
Ask for a quotation or demo Uniformly portion huge tissues & sample arrays Megatome is the only microtome that may segment samples as huge as intact nonhuman primate and human organs, which makes it a must have for fields which include neuropathology.
Operating the CLI directly from a Gradle job is not currently supported. A distribution have to be made by means of gradlew :j2d-cli:distZip to make a zip file that contains almost everything required to operate.
SE takes advantage of a rotational electric powered subject to disperse really electromobile molecules (for instance antibodies or surfactant micelles) in the course of a porous sample with no harmful electrically charged structures within the tissue. This allows 2-4 day clearing of intact organs,
Our preformulated EasyIndex Alternative raises and homogenize the refractive index of delipidated tissue samples, rendering them thoroughly clear. This enables light penetration into your sample and makes certain the acquisition of large-resolution, in-concentrate graphic facts.
Megatome is really a megatomi.com novel microtome which allows for prime-precision sectioning of a variety of tissue samples – from organoids, to arrays of animal organs, to intact human Mind hemispheres – with minimal tissue problems and data decline.
It’s time and energy to improve your microtome to Megatome. With correct higher-frequency slicing for an unmatched choice of sample measurements and kinds – from organoids and tumors to expanded tissues, sample arrays, and intact primate organs – Megatome is optimized for various purposes.
Totally delipidate total mouse brains or comparably sized samples in just one working day with SmartBatch+, or in one week with our passive clearing package.
Docset creation involves at minimal two selections: the name on the docset and the location with the Javadoc data files to incorporate from the docset.
This may develop a docset named Sample in The existing directory. Docset development is usually personalized with optional arguments:
Protect avoids the variability of hydrogel embedding and the information reduction from PFA preservation, shielding specimens for multiple rounds of processing.
--displayName: Will set the identify as demonstrated in Sprint. This really is useful when you make a docset with name SampleProject but Screen title Sample Challenge instead. This environment will default to the worth of --identify if omitted.
Our novel SHIELD tissue preservation method kinds intramolecular bonds employing polyfunctional, adaptable epoxides to stabilize tissue architecture and safeguard the sample’s endogenous fluorescence, protein antigenicity and nucleic acids.