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Group I was the SD1 (GA) mediated pathways controlled by 6 independent FGUs, QPh2a, QPh3b, QPh4a, QPh7b, QPh12 and QG1-3 (QPh9b and QPh9b) which expressed (detectable) only in the presence of SD1 (Fig. 2, Tables S11, S12, S13).
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AS1 is expressed only in emerging lateral organ primordia, and in seeds its expression is detectable only in limited subepidermal cells corresponding to cotyledon initials at the heart stage [ 48].
HaCaT cells expressed detectable levels of TMEPAI only in the presence of more than 8 h of TGF-β stimulation; there were no detectable levels of TMEPAI without TGF-β stimulation (Fig. 1a).
Despite their clonal origin, only 50 60 percent of the cells expressed detectable PyLT even in continued presence of the selective agent.
Transgene expression was detectable only in lung tissue (Figure 2A).
Only results for clones which expressed detectable amounts of PglB in DWP are shown (analysed by anti-HA Western blot).
Furthermore, in vivo phosphorylation of endogenous BRCA2 at T77 was detectable only in cells expressing full-length WT BRCA2, and not in BRCA2-defective cells, including EUFA423 cells, which express an equivalent amount of BRCA2 lacking only a short region of the CTD.
In the mixed C57Bl6/CBA background, Alb-Cre micexpressededetectablele amounts of the transgene only after birth.
1H9 mAb exclusively detected spots consistent with endogenous murine 3UIM ataxin-3 (pI 4.69, MW of 40.5 kDa), mono-ubiquitinated 3UIM ataxin-3 (pI 4.81, MW ∼8 kDa greater than the major transprotein and detectable only in the abundantly expressing MJD15.4 brain), and putative smaller ataxin-3 splice isoforms or degradation products (apparent MW of <37 kDa).
The transfer of the C from [1-C]-α-ketoglutarate to [1-C]-2-hydroxyglutarate was detectable only in tumor cells expressing mutant IDH1.
RT-PCR expression analyses by using total RNA isolated from root, shoot and flower showed that the FDRMADS6 transcript was detectable only in flower while FDRMADS7 was expressed in all three tissues.
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