megatomi.com - An Overview
megatomi.com - An Overview
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Our new Very clear+ tissue clearing technique is the only real approach that delipidates samples with no change in morphology and with negligible effect on structural integrity.
Megatome is actually a vibrating microtome created to segment a broad selection of samples, from organoids and biopsy samples to expanded rodent brains and intact human organs. With superior blade vibrating frequency and minimized blade deflection, Megatome enables superior-throughput tissue sectioning with uniform surface area profile, as well as minimal tissue hurt and information decline.
Request a quote or demo Uniformly segment huge tissues & sample arrays Megatome is the only microtome which can part samples as huge as intact nonhuman primate and human organs, making it priceless for fields like neuropathology.
Megatome is suitable for precision: the blade vibrates at a greater frequency and bigger amplitude array than other microtomes, and features a exceptional deflection Management mechanism.
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Our preformulated EasyIndex Alternative raises and homogenize the refractive index of delipidated tissue samples, rendering them absolutely clear. This allows light-weight penetration into your sample and makes sure the acquisition of superior-resolution, in-concentrate picture info.
Megatome is usually a novel microtome that enables for prime-precision sectioning of an array of tissue samples – from organoids, to arrays of animal organs, to intact human brain hemispheres – with negligible tissue problems and data loss.
eFLASH is a immediate tissue labeling procedure that enables for uniform entire-organ staining in 20 rounds of labeling.
The SmartSPIM mild sheet microscope offers unparalleled resolution and acquisition velocity through intact tissue volumes, although its modular design helps you to up grade and customize individual parts.
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Our novel Protect tissue preservation technique types intramolecular bonds employing polyfunctional, adaptable epoxides to stabilize tissue architecture and safeguard the sample’s endogenous fluorescence, protein antigenicity and nucleic acids.