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The results of Unconfined Compressive Strength (UCS) and Resilient Modulus (MR) testing of these geopolymer stabilized CB and RCA aggregates indicate that different mixtures of CCR based geopolymers can be used to improve the strength properties of the C&D aggregates for pavement base/subbase applications.
Semiquantitative EDS analyses, as transects across the film, and compositional mapping of the aggregates indicate that the binding film consists of an amorphous phase rich in S and Fe and minor P, with variable amounts of K, Ca, Na, and Mg, depending on the particle to which they adhere.
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As predicted, OMmCherry, OMsfGFP and PERImCherry retained their envelope localization when IMmCherry probe formed fluorescent cytoplasmic aggregates, indicating that following plasmolysis only the IM fusions collapse with the inner membrane.
Strikingly, the filter assays revealed that cell extracts with insoluble Rnq1Q54 or Rnq1Q91 aggregates also contained SDS-stable Sup35 aggregates, indicating that formation of polyQ-tagged Rnq1 aggregates indeed stimulates the aggregation of Sup35, which contains a heterologous Q/N-rich prion domain.
The characterization results confirmed the effective and relatively uniform functionalization of the MWCNTs despite formation of aggregates, indicating that OFM provides a viable approach for functionalizing MWCNTs.
In vivo culture of explants resulted in the induction of Dspp within the cell aggregates indicating that tooth tissue was present.
In vitro culture of these recombinant explants resulted in the induction of early tooth marker genes in the cell aggregates, indicating that the cells were able to respond to the odontogenic signals produced by the oral epithelium.
A comparison between limestone and siliceous aggregates indicates that the former often provide higher measured compressive strengths at equivalent levels of hydration, even when the two aggregate types exhibit similar elastic moduli.
PrPmyc antagonized the toxicity of truncated PrP, restored prion infectibility of PrPC-deficient mice, and was physically incorporated into PrPSc aggregates, indicating that it possessed all functional characteristics of genuine PrPC.
Autophagy deficient mice lacking p62/SQSTM1 failed to form ubiquitin positive aggregates, indicating that p62/SQSTM1 is important for aggregate formation [ 235].
However, the observation that treatment with Triton X100 does not disperse the aggregates indicates that they are not simple membrane-bound vesicles.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com