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Distinct time-resolved fluorescence signals of the AuNP-quenched NPF polymers at different values of pH confirmed the interactions between these species.
FTIR and SEM-EDX techniques confirmed the interactions between lead ions and functional groups on the wall surface of Klebsiella sp. 3S1.
Similarly, ChIP-PCR validations were performed in wild-type hNSCs, and the result confirmed the interactions between the endogenous AICD and these regions.
In addition, reciprocal analyses with anchors at fragment 4 in neonatal heart and at fragment 2 in neonatal brain confirmed the interactions between these sequences with the Kcnq1 promoter region, underscoring the presence of tissue-specific conformations.
Finally, we confirmed the interactions between ERα/PI3K and ERα/Src using the ERα-positive cell lines CLB-SAV, ZR75.1 and Cama-1 as well as the ERα-negative cell line MDA-MB-231.
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We then confirmed the interaction between FOXO3a and ER using co-immunoprecipitation and immunoblotting assays.
To further confirm the interaction between OsMPK20-4 and OsMPK3, co-immunoprecipitation (Co-IP) assay was performed.
By this experimental technique, we confirmed the interaction between HP1β and UBF1 (reference interacting partners were HP1β and H3K9me3).
FTIR analysis confirmed the interaction between CCNWs and AgNPs.
In addition, co-immunoprecipitation with anti-LSD1 antibody confirmed the interaction between LSD1 and Nrf1 in 3T3-L1 LSD1 3T3-L1 LSD1 (Fig. 3c).
A FLAG pulldown from cells expressing CSA-FLAG followed by western blot analysis confirmed the interaction between CSA and the TRiC subunit TCP1 (Fig. 1b).
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