MEGATOMI.COM - AN OVERVIEW

megatomi.com - An Overview

megatomi.com - An Overview

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Our new Obvious+ tissue clearing approach is the only method that delipidates samples without having adjust in morphology and with minimum impact on structural integrity.

Our transform-essential SmartBatch+ method brings together electrophoretic tissue clearing and immunolabeling into one particular higher-throughput machine.

Antibodies might choose weeks to diffuse as a result of just a few millimeters of tissue, with a steep labeling gradient from floor to core.

Megatome is created for accuracy: the blade vibrates at an increased frequency and larger amplitude variety than other microtomes, and features a exceptional deflection Management mechanism.

SE makes use of a rotational electric industry to disperse very electromobile molecules (such as antibodies or surfactant micelles) in the course of a porous sample without having detrimental electrically billed structures inside the tissue. This permits two-4 day clearing of intact organs,

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It’s time to improve your microtome to Megatome. With precise significant-frequency slicing for an unmatched variety of sample measurements and kinds – from organoids and tumors to expanded tissues, sample arrays, and intact primate organs – Megatome is optimized for various apps.

The SmartSPIM gentle sheet microscope supplies unparalleled resolution and acquisition pace during intact tissue volumes, while its modular design allows you to enhance and personalize personal components.

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Protect avoids the variability of hydrogel embedding and the knowledge loss from PFA preservation, protecting specimens for many rounds of processing.

Leverage the Apparent+ tissue clearing megatomi.com strategy, together with eFLASH and patented stochastic electrotransport systems, to swiftly apparent and label complete organs. Key highlights and characteristics include:

Our novel Protect tissue preservation method varieties intramolecular bonds using polyfunctional, versatile epoxides to stabilize tissue architecture and safeguard the sample’s endogenous fluorescence, protein antigenicity and nucleic acids.

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