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The new reagents are easier to synthesize than the previous reagents and have been made on the multigram scale appropriate to support worldwide newborn screening.
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Positions are available for reagent addition (with connections from the previous cassette, reagent vials, or external delivery lines), evaporation (with connections to inert gas and the vacuum system), transfer (with connections to inert gas and a dip tube), and sealed reactions (with no fluidic connections).
In previous research, reagent-grade chemicals have been used as the iron source in magnetite nanoparticle synthesis, which presents an economic challenge to the application of this technology in areas such as water and wastewater treatment.
Following the same principle as in the previous case, these reagents could reduce the sulfonium salt to generate a CF3 radical which reacted with styrene so that after oxidation with air, trifluoromethylated ketones were generated in moderate yields (21 39%).
Concentrations and exposure times were chosen on the basis of previous experience of these reagents on transport in other cells [20], [25], and to minimize deleterious effects on HEK-293 cell viability.
Immunoblotting experiments reveal that antibodies deemed specific for NB react in fact with either albumin, fetuin-A, or both, indicating that previous studies using these reagents may have detected these serum proteins from the same as well as different species, with human tissue nanoparticles presumably absorbing bovine serum antigens from the culture medium.
The regression analysis were controlled for the type of reagent (the use of Innovin versus other reagent) since previous research showed that use of Innovin may systematically give different results on the measured INR [ 18].
In previous work, the deblocking reagent was light, and it was contained to a specific region of the chip by masking techniques.
In addition, compound 5 with a choline moiety that we used as derivatization reagent in previous work [ 28] was also investigated with the complete system.
We designed a MO targeted against both pseudoalleles of the X. laevis Gsc gene, which should provide a better tool than the more indirect loss-of-function reagents used by previous workers.
These modifications may have been necessary due to the carry over of primers and reagents from the previous PCR reactions (Fig. 1A) and the complexity of the DNA mixture in the AFP.
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