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The same binding pattern was observed for U36 as expected.
Similar binding pattern was observed with ETS-1 oligo and nuclear extract from mouse αTN4-1 cells (data not shown).
Similar binding pattern was observed with AP-2α oligo and nuclear extract from mouse αTN4-1 cells (data not shown).
On the whole, no modification of the CycG binding pattern was observed (data not shown) suggesting that CycG recruitment does not depend on Corto.
Similar binding pattern was observed with SP-1/SP-3 oligo and nuclear extract from mouse αTN4-1 cells (data not shown).
Similar binding pattern was observed in reciprocal co-immunoprecipitation experiments where syntaxin4 was immunoprecipitated and binding of Munc18c determined.
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We rephrased the sentence in question and now write: "The only notable deviation from the FG-binding pattern was observed with MtNup188, which was relatively inefficiently eluted with 1M NaCl from Nup100 1-310) and Nup100 1-610), suggesting that MtNup188 either interacts with these FG-repeat regions more tightly than ScKap95 or that these interactions are more hydrophobic in nature".
The only notable deviation from the FG-binding pattern was observed with MtNup188, which was relatively inefficiently eluted with 1M NaCl from Nup100(1 310) and Nup100(1 610), suggesting that MtNup188 either interacts with these FG-repeat regions more tightly than ScKap95 or that these interactions are more hydrophobic in nature.
As the coating concentration increased from 0.1 to 10 μM, no noticeable cell-binding pattern was observed on the plot for [V7]20; the data did not fit to either a linear first order (r = 0.582) or hyperbolic (r = 0.816) regression.
Unexpected binding patterns are observed for oligonucleotides.
Similar binding patterns were observed near the AGR3 gene.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com