megatomi.com Secrets
megatomi.com Secrets
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Our new Apparent+ tissue clearing system is the one strategy that delipidates samples without having improve in morphology and with small effect on structural integrity.
Megatome is actually a vibrating microtome designed to portion a wide array of samples, from organoids and biopsy samples to expanded rodent brains and intact human organs. With substantial blade vibrating frequency and minimized blade deflection, Megatome permits superior-throughput tissue sectioning with uniform area profile, as well as minimal tissue harm and data reduction.
Antibodies may well acquire months to diffuse by only some millimeters of tissue, that has a steep labeling gradient from area to core.
Megatome is made for accuracy: the blade vibrates at a greater frequency and larger amplitude range than other microtomes, and features a unique deflection control mechanism.
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Megatome can be a novel microtome that allows for top-precision sectioning of an array of tissue samples – from organoids, to arrays of animal organs, to intact human brain hemispheres – with small tissue harm and knowledge reduction.
It’s time for you to upgrade your microtome to Megatome. With precise high-frequency slicing for an unmatched choice of sample sizes and kinds – from organoids and tumors to expanded tissues, sample arrays, and intact primate organs – Megatome is optimized for varied purposes.
Thoroughly delipidate entire mouse brains or comparably sized megatomi.com samples in only one day with SmartBatch+, or in a single week with our passive clearing kit.
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Both down load a release or produce a distribution zip as outlined earlier mentioned. Unzip the archive to a preferred spot.
Leverage the Apparent+ tissue clearing method, in addition to eFLASH and patented stochastic electrotransport systems, to swiftly obvious and label total organs. Vital highlights and attributes contain:
Our novel Defend tissue preservation procedure sorts intramolecular bonds using polyfunctional, flexible epoxides to stabilize tissue architecture and safeguard the sample’s endogenous fluorescence, protein antigenicity and nucleic acids.