br Data Dataset provided in

Data Dataset provided in this article shows the NMR spectra for compounds extracted from native Australian plants species Pilidiostigma glabrum, Myoporum montanum, Geijera parviflora, and Rhodomyrtus psidioides. In addition to collagen synthesis [5], additional analysis was performed to determine keratin expression. Data is included that shows keratin 1, 5, 10 and 14 protein INCB028050 in the cultured human keratinocyte cell line (HaCaT).
Experimental design, materials and methods
Acknowledgements This study was supported by the Wound Management Innovation Cooperative Research Centre. AJC is supported by a Senior Research Fellowship (GNT#1002009) from the National Health and Medical Research Council of Australia.
Data The data display the characterization of starch and silver nanoparticles synthesized by starch under different condition. Also, UV–vis spectra of Fe3O4 NPs, supernatant and starch with iodine are demonstrated.
Experimental design, materials and methods
Acknowledgment The authors wish to acknowledge Tarbiat Modares University of Iran (TMU) and Iranian Nanotechnology Initiative Council for their financial support towards major research projects.
Specifications table
Value of the data
Data Datasets provided in this article represent reliability of unauthorized genetically modified (GM) papaya (Carica papaya L.) line PRSV-YK detection method (PRSV-YK detection method), including papaya endogenous gene, Chymopapain (Chy), detection method, using real-time polymerase chain reaction (PCR). Table 1 presents specificity of PRSV-YK and Chy detection methods. Fig. 1 shows that Chy detection method amplified papaya DNA, but both PRSV-YK and Chy detection methods did not amplify rice, soybean, maize, potato, rapeseed, pineapple, peach or passion fruit DNA. Fig. 2 presents sensitivity of PRSV-YK detection method. Cycle threshold (Ct) values obtained from real-time PCR amplification plot were quantitative (R2=0.99) in the range of 0.01–100% line PRSV-YK DNA concentrations. Table 2 presents results of homogeneity test on prepared samples. Table 3 presents statistical data obtained from homogeneity test on prepared samples. Table 4 summarizes interlaboratory validation data. Data were statistically analyzed to determine mean, relative standard deviation (RSD), repeatability RSD (RSDr) and reproducibility RSD (RSDR) from Ct values obtained [1].
Experimental design, materials and methods
Acknowledgment This work was supported by a Grant from the Ministry of Health, Labour and Welfare of Japan. We would like to thank following laboratories for participating in interlaboratory validation: Tokyo Metropolitan Institute of Public Health (Tokyo, Japan), Food and Agricultural Materials Inspection Centers (Saitama, Japan and Kobe, Japan), Saitama Prefectural Institute of Public Health (Saitama, Japan), Yokohama City Institute of Health (Yokohama, Japan), Kanagawa Prefectural Institute of Public Health (Chigasaki, Japan), Kawasaki City Institute of Health (Kawasaki, Japan), Japan Frozen Foods Inspection Corporation (Yokohama, Japan), Japan Food Research Laboratories (Tama, Japan) and Japan Inspection Association of Food and Food Industry Environment (Tokyo, Japan).
Data The data file in the format Excel 2010 contains two spreadsheets; the first showing the records of myxomycetes, the second the parameters measured or estimated for the trees of Picea glauca in the 1ha plot. All columns are explained by comments in the heading field. Specimens were determined according to standard literature, nomenclature follows [2].
Experimental design, materials and methods All 380 trees of Picea glauca in the selected plot of 100×100m2 were mapped with a differential GPS (Trimble R3) in July 2012, allowing a precision of <=30cm (floating mode and post processing). From 260 of the 380 Picea glauca trees in the plot about 20–30 bark pieces around each trunk (to minimize possible differences related to different exposition of N-or S-facing sides of the trunk) were sampled between 1.2 and 1.5m height; This height was chosen to exclude soil-inhabiting myxomycetes, where plasmodia often migrate to elevated points to fruit. Sampling included nearly all larger trees (dbh>4cm); the majority of the 120 trees not sampled was below 0.5cm dbh or were saplings not reaching sampling height. The outermost, dead bark and bases of small dead branches were carefully removed without injuring the living part of the tree. Bark samples were air dried in paper bags and transported back in the laboratory.