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Light dark shift experiments showed that light contributed to the electricity generation.
The acid shift experiments were conducted with MC4100 ΔtatABCDE containing an arabinose-inducible TorA-GFPmut3* plasmid (Fig. 2A, B) [4].
This result indicated that both binding surfaces of Hfq were in use and validated the competition gel shift experiments.
Our gel shift experiments suggest that PUF60 and U2AF65/35 may bind sequentially, rather than simultaneously to the RNA.
Gel shift experiments with recombinant dTCF demonstrated that the introduced mutations eliminated dTCF binding (data not shown).
By UV cross-linking and band shift experiments, we have shown that both M1 and R1 can be specifically recognized by a 40 kDa SR.
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To test if binding of p33 to RII-SL is affected by CPZ and QC, we performed in vitro gel-shift experiments with purified components.
We performed gel-shift experiments with U2AF65/35 heterodimer purified from baculovirus-infected SF9 cells and recombinant PUF60 purified from human HEK-293E cells (Figure S5).
ALC performed the sequential batch and linear-temperature-shift experiments.
Temperature-shift experiments of glp-1 q224 glp-1 q224dites.
Temperature-shift experiments of emb-30 tn377ts) emb-30 tn377ts.
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