A Review Of megatomi.com
A Review Of megatomi.com
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Our new Obvious+ tissue clearing approach is the only process that delipidates samples without adjust in morphology and with minimum impact on structural integrity.
Megatome is a vibrating microtome meant to part a broad range of samples, from organoids and biopsy samples to expanded rodent brains and intact human organs. With significant blade vibrating frequency and minimized blade deflection, Megatome allows high-throughput tissue sectioning with uniform area profile, and also minimum tissue destruction and data loss.
Antibodies might acquire weeks to diffuse by only a few millimeters of tissue, that has a steep labeling gradient from surface to core.
Megatome is designed for accuracy: the blade vibrates at the next frequency and larger amplitude selection than other microtomes, and features a exclusive deflection control mechanism.
SE takes advantage of a rotational electric discipline to disperse really electromobile molecules (like antibodies or surfactant micelles) through a porous sample without the need of damaging electrically charged constructions in the tissue. This allows two-4 day clearing of megatomi.com intact organs,
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Megatome is usually a novel microtome which allows 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 really a immediate tissue labeling procedure that enables for uniform entire-organ staining in twenty rounds of labeling.
Entirely delipidate entire mouse brains or comparably sized samples in only one day with SmartBatch+, or in one 7 days with our passive clearing kit.
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Defend avoids the variability of hydrogel embedding and the information reduction from PFA preservation, defending specimens for multiple rounds of processing.
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Our novel SHIELD tissue preservation procedure sorts intramolecular bonds applying polyfunctional, versatile epoxides to stabilize tissue architecture and safeguard the sample’s endogenous fluorescence, protein antigenicity and nucleic acids.