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Ligand binding data were analyzed using GraphPad Prism 4.03 (GraphPad Software , Inc.
The binding data were analyzed by a mathematical calculation based on the 1∶1 (Langmuir) binding model (Table 1).
The ligand binding data were analyzed by nonlinear least-squares regression using the computer program Graphpad Prism (GraphPad Software).
For agonist-stimulated [35S]GTPγS binding, data were analyzed with GraphPad Prism 4.0 software using nonlinear regression and sigmoidal curve fitting to obtain potency (EC50) and efficacy (Emax) values.
The binding data were analyzed with the 1 1 Langmuir binding model in the BIAevaluation software (BIAcore).
The binding data were analyzed by fitting the experimental points to the Eq. (2) using non-linear regression software Scientists from MicroMath Scientific Software Inc., (Saint Louis, Mo) in which χ-function between experimental and theoretical values of a mathematical model is minimized.
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The saturation binding data was analyzed with nonlinear regression assuming the one site specific binding model using the equation Y = Bmax*X/ Kd+X) using GraphPad Prism (GraphPad Software Inc. San Diego, USA). 1 mg/mL rCR2 and K41E CR2 were labeled with 400 MBq [99mTc(CO)3(OH2)3]+ for 30 min. at 37°C with gentle shaking.
Genome-wide binding data was analyzed with utilities in the cistrome portal.
To derive binding constants, data were analyzed by means of global fitting using BIAevaluation version 3.1 (Biacore AB).
To define the in vivo RNA recognition elements for WTAP and METTL3, the binding cluster data were analyzed by HOMER, a suite of tools for motif discovery and next-generation sequencing analysis.
To derive the binding parameters, obtained data were analyzed using modified Stern Volmer equation [24 26].
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binding data were downloaded
binding experiments were analyzed
binding data were entered
binding kinetics were analyzed
binding properties were analyzed
binding proteins were analyzed
binding data were subjected
binding partners were analyzed
binding data were binned
binding data were strengthened
binding data were used
binding data were corrected
binding curves were analyzed
binding data were compared
binding patterns were analyzed
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