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However, the failure of ELISA measurements of TGF-β3 in mouse serum indicate a concentration below the sensitivity of the assay (~0.1 ng/ml (Edin et al. 2014)).
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The larger bands were also co-immunoprecipitated with FK2, but not with mouse serum, indicating that the larger bands were probably Ub-LlPTPCs.
We selected candidate miRNAs that satisfied three criteria: (1) the level in DCKO mouse serum was >1.5-fold higher than that in controls; (2) the global normalisation value was >100 in DCKO mouse serum, indicating easily detectable levels of miRNAs; and (3) the identified miRNAs were coincidently upregulated in both sera and DGC tissues.
In contrast to previous observations with irradiated cells, the response to doses above the HRS-range was also affected by the mouse serum, indicating a higher concentration of TGF-β3 in the mouse serum than secreted by LDR primed cells (Edin et al. 2014).
Furthermore, SWAPs treated with anti-SjTGR antibodies expressed a lower TR enzymatic activity than untreated SWAPs, and the enzyme activity was not affected after incubating with normal mouse serum, indicating that anti-SjTGR antibodies influenced the thioredoxin reductase activity of SjTGR to catalyze DNTB into NTB, which can be measured at 412 nm.
Both homozygous and heterozygous hema6 mice exhibit elevated total bilirubin concentration in the serum, indicating increased hemolysis.
qRT-PCR for miR-1 and miR-206 in serum indicated that these miRNAs are 20/40-fold 20/40-foldn mdx with renrichedo WT mine (Fig 3D).
Both active bDAb preparations retained their original antigen-binding activity after incubation at 37 °C in mouse serum for up to 7 days, indicating excellent stability of the constructs.
Similarly, recombinant sialidase was not immunoreactive to mouse serum obtained from UV-killed P. acnes-immunized mice (Figure S2), indicating that the undetected immunogenicity was not due to denaturation of sialidase during the heat treatment.
Similarly, SEP54 antibody detected stronger signal in ob/ob mouse serum samples than that in WT mouse sample.
Experimental results indicate that the biosensor is able to detect recombinant H5 HA at 1.4 μM in 10% mouse serum, with high specificity for H5 as compared to H1 (H1N1 A/South Carolina/1/18).
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