Speedily attain sections as slim or thick as your application involves, without having stressing about dropping or distorting important tissue samples.
Megatome is often a vibrating microtome made to section a broad range of samples, from organoids and biopsy samples to expanded rodent brains and intact human organs. With large blade vibrating frequency and minimized blade deflection, Megatome allows superior-throughput tissue sectioning with uniform surface area profile, and also negligible tissue damage and information loss.
Request a estimate or demo Uniformly portion huge tissues & sample arrays Megatome is the one microtome which can portion samples as large as intact nonhuman primate and human organs, making it invaluable for fields like neuropathology.
Megatome is designed for precision: the blade vibrates at the next frequency and bigger amplitude array than other microtomes, and features a distinctive deflection Handle mechanism.
SE takes advantage of a rotational electrical area to disperse highly electromobile molecules (for instance antibodies or surfactant micelles) through a porous sample with no detrimental electrically billed buildings inside the tissue. This allows 2-four day clearing of intact organs,
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Megatome is actually a novel microtome that permits for prime-precision sectioning of an array of tissue samples – from organoids, to arrays of animal organs, to intact human brain hemispheres – with nominal tissue hurt and data reduction.
It’s the perfect time to enhance your microtome to Megatome. With exact higher-frequency slicing for an unmatched array of sample sizes and types – from organoids and tumors to expanded tissues, sample arrays, and intact primate organs – Megatome is optimized for various applications.
Entirely delipidate complete mouse brains or comparably sized samples in just one working day with SmartBatch+, or in one week with our passive clearing package.
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Our novel Protect tissue preservation system varieties intramolecular bonds working with polyfunctional, versatile epoxides to stabilize tissue architecture and safeguard the sample’s endogenous fluorescence, protein antigenicity and nucleic acids.