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To further explore whether active NF-κB can bind to its target DNA sequence and activate gene transcription in response to CCN2 stimulation, NF-κB DNA binding activity was determined by EMSA following incubation of HSC nuclear protein extracts with P-labeled NF-κB oligomers containing NF-κB/CBF1 binding sites.
NF-κB binding activity was determined using the Light Shift Chemiluminesencent EMSA kit (Pierce, Rockford, IL).
DNA binding activity was determined by EMSA using a consensus NF-κB IRDye-labeled oligonucleotide probe (LI-COR).
HIF-1 DNA binding activity was determined in RA FLS nuclear extracts.
NF-κB DNA binding activity was determined by transcription factor assay.
The NF- κB/DNA binding activity was determined with LightShift Chemiluminescent EMSA kit (Thermo Scientific, Rockford, IL, USA).
Similar(51)
The FA percentage content in A549 membrane phospholipids, content of COX-2, level of PPAR γ, and NF- κB binding activity were determined.
NFκB-RelA DNA-binding activity was determined by a TransAMTM NFκB-RelA kit (Active Motif) using 5 µg of nuclear extract proteins according to the manufacturer's instructions.
HIF-1 and -2, VEGF, and VEGFR-1 and -2 protein levels were determined using total tissue lysates, whereas HIF-1 DNA-binding activity was determined using nuclear extracts.
The NF- κB DNA-binding activity was determined by EMSA.
NF-κB DNA-binding activity was determined by gel mobility shift assay while NF-κB response gene expression was evaluated using a luciferase reporter.
More suggestions(15)
binding specificity was determined
binding reaction was determined
binding avidity was determined
binding constant was determined
binding sequence was determined
binding activity was verified
binding activity was increased
binding saturation was determined
binding activity was affected
binding activity was expected
binding model was determined
binding activity was accompanied
binding level was determined
binding pattern was determined
binding ability was determined
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