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In addition, this new method significantly simplified the purification step of the polymer products because of the convenient separation between inorganic particles and organic polymer solution.
Furthermore, the mathematical representation of the model allows convenient separation of the contribution of the equivalent linear and non-linear internal forces developed in the physical system.
The Ni microspheres were catalytically active in the reduction of 4-NP, and the unique morphology and strong magnetism ensured convenient separation from the reaction mixture either by simple filtration or with an external magnetic field.
It is noted that the antisense strand is cleaved into 20-nt monomers, and the sense strand is cleaved into monomers that are 25 or 30 nt in length, which allows convenient separation by chromatographic methods.
These multifunctional hollow carbon microspheres can realize rapid capture and convenient separation of low-concentration peptides.
With this system, it is now possible to sort homoeologous genes using a low-cost and convenient separation method, thus allowing large-scale PCR-based marker development for wheat.
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Finally, the filamentary recombinant E. coli was not only able to produce more P 3HB-co-4HB) from glucose but also allow convenient downstream seP 3HB-co-4HBm the fermentation broth.
The Ni@GSs-C CH3 2COONa Ni@GSs-C CH3 2COONagreat potenanocompositesfective absorbent for removing aromatic compounds from waste water owing to thadr rapid absorption rate, higreatsorpotentialasity, convenient manneffectiverabsorbent re-use property.
By combining the MNP-based rapid, efficient target capture and convenient magnetic separation and enzyme-based great signal amplification together with the careful optimization of the MNP surface and assay conditions, this assay can achieve direct, label-free quantitation of T-DNA down to 50 fM level with a total assay time of <3 h (via fluorescence readout).
This assay uses a pair of specific DNA probes, one being covalently conjugated to an MNP for target capture and the other being linked to an enzyme for signal amplification, to sandwich a DNA target, allowing for convenient magnetic separation and subsequent efficient enzymatic signal amplification for high sensitivity.
Additional advantages here include (1) the use of MNP-based homogeneous, rapid target capture, (2) convenient magnetic separation for low assay background, and (3) the use of large excesses of MNP cDNA/En sDNA probes to push T-DNA hybridization equilibrium toward the captured state, allowing efficient capture and detection of T-DNA at concentrations well below the corresponding Kd.
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