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To identify proteins that specifically interact with PPM, we tested the interaction of cell extracts with labelled phospholipid-containing PPM or IPM in a ligand blotting assay.
We therefore tested the interaction of ORF38 with other tegument proteins and found out that ORF38 interacts with ORF33, consistent with a previous report (Lee et al., 2011).
Using a co-integration Granger causality test, Zhizhen & Xiuquan (2010) empirically tested the interaction of the exchange and stock markets.
In addition, we tested the interaction of Rb with an HA-tagged protein corresponding to Orc1 mutated in the LxCxE domain (HA-Orc1 LPGRK).
To test this hypothesis, we cloned and expressed a set of CLL BCRs expressing common stereotyped HCDR3 sequences (subsets 1, 3 and 7 according to Stamatopoulos [19] and Murray [38]) and tested the interaction of these antibodies with lysates of a set of different cell types including stromal cells.
To validate this result, we tested the interaction of STAG1 with Nanog by co-immunoprecipitation of GFP versus an IgG control in Nanog-LAP ESCs as well as in wildtype ESCs and confirmed the specific interaction in Nanog-LAP cells (Fig. 6B,C).
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Thus, in this study, we first tested the interactions of the unmodified H3K4 peptide with full-length KDM5B or its truncated variants through a biotin-labeled peptide binding assay.
To test the specificity of the Txnip-PDI interaction, we tested the interactions of PDI, PDIA3, PDIA4, PDIA13, and PDIA15 with Txnip.
We tested the interactions of endogenous iASPP with p300 and TAp73 in untreated as well as cisplatin-treated HCT116 cells.
Tissue phantoms are commonly employed to test the interaction of electromagnetic radiation and biological tissue[27].
We wanted to test the interaction of tree species richness and structure in particular.
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