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Thus, this glucose oxidase assisted homogeneous electrochemical drug receptor binding assay has been proved to be a useful tool for drug screening.
Annexin binding assay has been used to measure the number of apoptosis and necrotic cells.
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Glycans on α-DG recognized by both the antibodies and laminin binding assay have been widely referred to as the functional glycans [24].
Although CHA has been reported to block [H]DPCPX binding at A1R with a Ki of approximately 5 n m in rat hippocampus (Maemoto et al., 1997), according to our data, higher EC50 values for different A1R agonists in the [S]GTPγS binding assay have been found (Lorenzen et al., 1996; Cordeaux et al., 2004).
The cell-binding assay has been previously utilized to describe interactions between DCC and netrin-1 in the binding site 1 and binding site 2 (Finci et al., 2014).
Radioligand binding assays have been used to study their affinity for opioid (μ, δ and κ) and I2-imidazoline receptors.
Specific rapid filtration binding assays have been useful for almost 30 years both for drug discovery and understanding molecular mechanisms of drug action.
The endocrine data as well as the uterine receptor determinations by binding assays have been published previously [ 17].
Several experimental techniques, such as X-ray crystallography, nuclear magnetic resonance, and filter binding assays have been used to identify RNA-binding proteins.
Large-scale quantitative in vitro kinase binding assays have been developed to capture the complex interactions between inhibitors and kinases[ 15- 17].
Zona pellucida binding assays have been used to predict fertility in humans [ 3] and animals, for example cattle [ 4], dogs [ 5- 8] and cats [ 9- 11].
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