Our new Apparent+ tissue clearing technique is the only process that delipidates samples with no improve in morphology and with small effect on structural integrity.
Megatome is usually 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 high blade vibrating frequency and minimized blade deflection, Megatome permits substantial-throughput tissue sectioning with uniform surface area profile, together with negligible tissue destruction and information loss.
Ask for a quotation or demo Uniformly section large tissues & sample arrays Megatome is the one microtome that can part samples as large as intact nonhuman primate and human organs, which makes it priceless for fields such as neuropathology.
Megatome is suitable for accuracy: the blade vibrates at a greater frequency and bigger amplitude vary than other microtomes, and includes a special deflection Regulate system.
SE works by using a rotational electrical discipline to disperse very electromobile molecules (like antibodies or surfactant micelles) throughout a porous sample without harming electrically billed constructions throughout the tissue. This permits 2-four working day clearing of intact organs,
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eFLASH is actually a rapid tissue labeling procedure that permits for uniform full-organ staining in twenty rounds of labeling.
The SmartSPIM light sheet microscope delivers unparalleled resolution and acquisition speed in the course of intact tissue volumes, whilst its modular structure permits you to enhance and personalize unique elements.
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Leverage the Crystal clear+ tissue clearing method, together with eFLASH and patented megatomi.com stochastic electrotransport technologies, to promptly apparent and label whole organs. Important highlights and characteristics include things like:
Our novel Protect tissue preservation technique types intramolecular bonds employing polyfunctional, versatile epoxides to stabilize tissue architecture and safeguard the sample’s endogenous fluorescence, protein antigenicity and nucleic acids.