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Immunohistochemistry was performed on formalin-fixed, paraffin-embedded (FFPE-) 4 μm TMA sections of tumour tissue specimen transferred to glass slides.
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Laboratory professionals reported better proportions of desirable practices than non-laboratory professionals with regard to specimen transferring from the barrel of the syringe in to test tubes (p < 0.001), specimen transport (p = 0.005) and specimen mixing with additives (p < 0.001).
On the other hand, mixing specimens with additives (63.4%, n = 64) and specimen transferring from syringes to test tubes (63.4%, n = 64) were activities that involved the highest proportions of undesirable practice among laboratory professionals in this phase (Table 2).
However, in the post collection phase, specimen transferring from syringes to test tubes (15.8%) and mixing specimen with additives (63.4%) involved highest proportions of undesirability among laboratory and non-laboratory professionals respectively.
Immunohistochemistry was performed on formalin-fixed paraffin-embedded 4- μm sections of tumour tissue specimens transferred to Menzel Menzel GmbHPlus (Gerhard Menzel GmBraunschweigweiGermanyany) slides essentially as described previously (Mansilla et al, 2007).
Options after closure include destroying the specimens, transferring them to another facility, or letting them sit unused in freezers.
Specimen transfer to another sample is not needed and contamination is avoided.
In either case, specimens are transferred between the ETH central chamber and the LEAP via the specimen transfer rod (Fig. 1a, 4).
In addition, the correlation accuracy between cryo-FM and cryo-EM would be reduced during the current specimen transfer procedure.
The 'touch-free' specimen transfer via cryo-EM holder allows least specimen deformation and thus maximizes the correlation accuracy between cryo-FM and cryo-EM.
The results are specimen transfer functions that relate propeller sources, having general spectral characteristics, to hull excitation.
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