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The DNA binding properties of three cation-substituted anthrapyrazole derivatives of emodin with calf thymus DNA were characterized by spectroscopic methods and the specific binding modes were elucidated.
The binding properties of three CBMs, X-2, X-6 and X-13, all selected using the insoluble part of birch wood xylan as a selection target were further investigated in this work with the aim of defining the potential to use such modules in analysis of xylans in plant tissues.
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We characterized the conformational stability of recombinant human NGAL and the solution phase binding properties of six monoclonal antibodies.
In this study, we compared the stability and protein binding properties of two recombinant antibody fragments with their parental monoclonal antibody.
This study describes HSA binding properties of two cyclometalated platinum (II) complexes with non-leaving lipophilic ligands; deprotonated 2-phenylpyridine (ppy): C1 and deprotonated benzo [h]quinolone (bhq): C2, using UV vis, fluorescence and circular dichroism (CD) spectroscopy.
In addition, FSK treatment did not influence translocation dynamics of the GR although it is known that PKA activation can modulate the steroid sensitivity by enhancing DNA binding properties of GR [19].
The binding properties of eight different Fabs directed against BMPR-IAEC were analyzed using surface plasmon resonance and with respect to their BMP-2 neutralizing activity, using an alkaline phosphatase (ALP) expression assay.
We therefore investigated how such engineering affected production and ligand binding properties of two well characterized TCRs fused to Ig.
Owing to results from the binding capability and enhancement of catalytic function when fused to CelE, we further studied the binding properties of four CBMs: CBM3a; CBM6; CBM30; and CBM44.
Exposure to antidepressants was further subclassified into four clusters based upon pharmacological binding properties of six common transporter or receptor sites: the 5-HT (serotonin) reuptake transporter, norepinephrine reuptake transporter, M3 receptor, H1 receptor, α1 receptor and 5-HT2c receptor [ 14].
Using a fluorescence anisotropy-based DNA-binding assay, we examined the DNA-binding properties of two engineered zinc finger proteins that differ by a single amino acid.
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