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The competitive binding assay implied that the fluorescence intensity was correlated with the amount of HLA-DR on the surface of APC.
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The assay implied that miR-15b could induce apoptosis in U87 and L229 glioma cells.
However, cytokine production assays imply that some antigen-specific effector function is retained.
Reciprocal cross-species transient expression assays imply that changes have also evolved in the set of transcription factors that interact with the Endo16 promoter.
The FLECS assay is a simple binding assay that enables proteins tagged with fluorophors to be rapidly and quantitative screened against small-molecule libraries.
Although the basic functions of the Obg subfamily proteins are not clearly established, the majority of bacterial Obgs have been commonly found to be associated with ribosome, in specific binding of Obg with ribosomal protein L13 was proved through an affinity blot assay method, implying that those proteins fundamentally could play a role in ribosome assembly or maturation [12], [16] [22].
The assumption that k is binding implies that education increases.
A large thermodynamic barrier limits SM binding, implying that significant conformational rearrangements are involved.
This implied that the binding epitope may be localized in hGH.
These results implied that heme-binding stabilized the protein to proteolysis.
Exogenous and endogenous binding assays showed that ULK1 interacts with PKCα (Supplementary Figure 2a, b).
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CEO of Professional Science Editing for Scientists @ prosciediting.com