Visualization 2.mp4

Color dynamic holographic display

Visualization 1.mp4

dynamic holographic displa

Photo-, Thermo-, Electrochromic, Erasable Inkless Printing, Ions Detection, and UV Detector Properties of Viologen Compounds Based on Homomolybdate/Keggin POMs

Three POMs-based viologen compounds with different structures were successfully constructed under solvothermal and hydrothermal conditions, [Cu(1,4-cby)2(H2O)0.5(β-Mo8O26)0.5]·C3H7NO·3H2O (1), [H2(1,4-cby)2]·(β-Mo8O26) (2) (1,4-cby·Cl = 1-(4-carboxybenzyl)-4,4′-bipyridine chloride), [H2(1,4-cbyy)2]·(SiMo12O40) (3) (1,4-cbyy·Cl = 1-(4-cyanobenzyl)-4,4′-bipyridine chloride). Compound 1 is a structure with the number “eight-like” metal–organic chain with Cu as the nodes, and compounds 2 and 3 are fascinating structures connected by hydrogen bonding interactions. More importantly, compounds 1–3 exhibit a good response to both light and electricity and the thermal response of compound 1 was also studied. The reasons for the response of compounds 1–3 to external stimuli were analyzed through methods such as UV–Vis, EPR, and XPS. In addition, the transient photocurrent response results of compounds 1–3 are the same as those obtained from kinetic calculations. Meanwhile, the coated filter paper based on compound 3 has been successfully applied in erasable inkless printing and anti-counterfeiting, the test paper of 3 can also detect metal ions, and the films based on compounds 1–3 are a flexible and portable ultraviolet (UV) detector

Semi-quantitative RT-PCR analyses on selected transcripts differentially expressed between fetal and adult livers.

<p>Equal amounts of starting RNA were reverse transcribed and subject to semi-quantitative PCR. PCR cycles were adjusted depending on transcripts abundance. Fetal (series 1 and 2: F1 and F2) and adult liver (A) PCR results were compared by agarose gel electrophoresis. Negative controls (N) were performed by using no RT templates. All PCR products were sequence confirmed.</p

Heatmap of pancreatic exocrine enzyme-related probe sets in series 2 data.

<p>Normalized log2 scale expression values for the probe sets representing transcripts related to pancreatic exocrine enzymes and zymogen secretion from series 2 data were plotted. Log2 scale data were used to facilitate viewing of all expression peaks. More dramatic variations in expression peaks in natural scale data led to improper viewing of those peaks on heatmap.</p

Heatmap of 66 probe sets representing clock and known rhythmic genes.

<p>Natural scale expression values from series 2 data for core clock genes and genes known to be rhythmically expressed in the adult liver were plotted with Heatmap builder. Some genes were represented by multiple probe sets. Phases were sorted by the “lag” values given by JTK_CYCLE.</p

Comparisons between fetal and adult liver transcriptomes.

<p>(<b>A</b>) Scatterplot of normalized and scaled average expression values in fetal (y-axis, series 2) and adult (x-axis) livers. Pairwise values for 22626 probe sets were plotted. <i>r</i> = 0.67, <i>P</i> = <0.01. (<b>B</b>) Fold differences in normalized and scaled average expression values between fetal (series 2) and adult (GSE11923) livers for 22626 probe sets. Ratios (fetal: adult) were plotted against their ranks.</p

Differential expression of clock genes between fetal and adult livers.

<p>Relative expression levels of selected clock genes, as detected by real-time RT-PCR results analyses on. Delta Ct values were converted to fold differences assuming amplification efficiency of 1.0. Adult expression level for each gene was set at 1.0.</p

Semi-quantitative RT-PCR analyses of pancreatic exocrine enzymes-related transcripts in fetal liver tissues.

<p>Equal amounts of starting RNA from the 12 time points of series 2 fetal liver tissues were reverse transcribed and subject to semi-quantitative PCR. PCR cycles were adjusted depending on transcripts abundance. Products were visualized by agarose gel electrophoresis.</p

Heatmap of the 145 rhythmic probe sets in series 2 microarray data.

<p>Series 2 natural scale expression values for the 145 probe sets that were rhythmic in both series of data (<i>p</i><0.1 by JTK_CYCLE) were plotted. Phases were sorted by the “lag” values given by JTK_CYCLE.</p