Fig. 4. Spectra of monochromatic light from the OLS

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Reflectance Spectroscopy Lab. Different colors correspond to different wavelengths of visible light 665 nm 630 nm 600 nm 550 nm 470 nm 425 nm 400 nm.

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Solar spectrum and absorption profiles of chlorophyll and bacteriochlorophyll pigments Solar spectrum and absorption profiles of chlorophyll and bacteriochlorophyll.

Fig. 3. Effect of NH4Cl (0 or 30 mM) on percentage of motile spermatozoa and VAP after 1 and 5 min after activation. Effect of NH4Cl (0 or 30 mM) on percentage.

Fig. 2. Outline of the two types of stimulus sequences employed in the analysis.(A) Environment information stimuli; (B) adaptation stimuli. Outline of.

Fig. 3. External work and kinetic and potential energy of the whole body for the mean individual (individual 10) in the mean population (population 1)

Fig. 1. Representative images of the four cell lines using fluorescence microscopy. Representative images of the four cell lines using fluorescence microscopy.

Fig. 4. E-cadherin expression level affects monomer dynamics.

Fig. 5. Effect of MPO on surface elasticity of human platelets

Fig. 2. Morphological changes of cultured adherent fibroblastic cells after OA treatment related to actin microfilament reorganization.(A) Cells observed.

Fig. 7. Motion adaptation increases time-dependent response modulations (TDRM) relatively to the average cell response.TDRM normalized to the value obtained.

Fig. 2. Proportion of motile objects and track length

Fig. 4. A primary screen based on scrape closure

Fig. 1. Blood lactate, blood glucose and blood corticosterone concentration from crawl until 4 hours of frenzy swimming in loggerhead (C. caretta) and.

Fig. 6. Comparison between the response against transformed tissues and capsule formation.At the cellular level the two responses share many similarities.

Fig. 2. Long-term CCH increases SDH activity after 6 weeks and does not prevent an increase of the fibre cross-sectional area.Fish were kept for 3 or 6.

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Table 1. Menthol preference index (MPI) and average number of eggs laid per female (EPF) in F0 and F1 lines.The statistical significance of MPI was assessed.

Fig. 10. Ratiometric live imaging of di-4-ANEPPDHQ in growing pollen tubes.(A) Higher and lower membrane order distribution in control and BCD treated.

Fig. 1. Mitochondrial internalization in cardiomyocytes.

Fig. 3. Read-outs of mTORC1 (P-S6(S235/236)) and mTORC2 (P-Akt(S473)) in wtPC12 and PC12-27 cells.(A,B) wtPC12 and PC12-27 cells were treated for 48 hr.

Fig. 1. Loss of PC following INT depletion

Fig. 4. The model of malate metabolism in fruit cells under different K level conditions. The model of malate metabolism in fruit cells under different.

Table 2. Cell surface abundance of β1 integrin measured by flow cytometry.DDR wild type and DDR over-expressing cells were treated with deoxymannojirimycin.

Fig. 1. E-cadherin localizes in nano-scale clusters.

Fig. 1. Pigmentation and melanophore counts of rainbow trout parr and smolt caudal fins.Pigmentation of (A) parr and (B) smolt. Pigmentation and melanophore.

Fig. 1. γ-Tubulin localizes in close proximity to centriole walls in interphase but within an extended PCM meshwork in mitosis.U2OS cells were fixed and.

Fig. 7. E2F1 acetylation in A1/A2-KO MEFs

Fig. 4. Brood size of four successive births by male seahorses Hippocampus erectus in the two groups (TR-1, TR-2).In TR-1 groups: male and female seahorses.

Table 3. Penetrance of cuticle defects seen in ush2 mutants embryos and in the progeny from rescue experiments (genotypes indicated in the table) with.

Fig. 5. The bulk of Cep135 localizes distantly from Sas-6 and STIL

Fig. 8. C. elegans susceptibility to α-terthienyl was affected by the activities of skn-1 and wdr-23. C. elegans susceptibility to α-terthienyl was affected.

Fig. 5. GFP fluorescence colocalization of Gcn5.

Fig. 2. Centrosomal proteins display distinct localizations and radial distances from centriole walls.U2OS cells were fixed and stained with the indicated.

Fig. 5. UV reflections from the eye cup.

Fig. 2. Soluble sugar and organic acid levels with different K fertilization during fruit development. Soluble sugar and organic acid levels with different.

Fig. 1. Aboveground biomass of Caragana and herbaceous plants, and proportional abundance of Caragana, under different grazing management treatments. Aboveground.

Fig. 4. BKA values for different species.

Fig. 7. Representative images of control (Cas9+GFP) and Cas9+gRNA+GFP co-injected embryos on day 4 of culture, showing nuclear-imported GFP (green) and.

Fig. 1. TSA at 165 nM induces maximal acetylation of histone H3 and near-maximal acetylation of histone H4.Immunoblot analysis of acetylated histones H3.

Fig. 4. Co-immunostaining of nocodazole or ASNase treated RPE-1 cells with anti-hASNS and anti-alpha tubulin showed defect in both mitotic spindle formation.

Table 1. Average ± S.E. of level of dissimilarity scores of each feature per stripe per pattern comparison of sides of the same fish (“Same Individual”),

Fig. 4. Schematic representing clock contribution to Fgf21 regulation in the liver. Schematic representing clock contribution to Fgf21 regulation in the.

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Fig. 2. Examples of changes in angular velocity and correlation coefficient during the O–O test. Examples of changes in angular velocity and correlation.

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Fig. 4. Perinuclear dynein regulators are not required for primary ciliogenesis.RPE cells were transfected with siRNA and either nocodazole-treated, fixed,

Fig. 1. Loss of PC following INT depletion

Fig. 2. RFC3 function in chloroplasts.

Fig. 2. RGD and KGD motifs in N. vectensis thrombospondins

Fig. 1. Generation of binarized movies of medaka behavior during the O–O test using the UMATracker program. Generation of binarized movies of medaka behavior.

Effect of chronic disturbance and acute stressor on testosterone levels. Effect of chronic disturbance and acute stressor on testosterone levels. (A) Testosterone.

Fig. 6. F1 trβ mutants accomplish natural metamorphosis.

Fig. 2. iPSCs produce functional osteoblasts.

Fig. 2. Effects of pH on percentage of motile spermatozoa and VAP after 1 and 5 min after activation. Effects of pH on percentage of motile spermatozoa.

Fig. 12. Overview of the molecular program essential to build mdDA neurons.The genes identified in this study (in red) have been added to the programming.

Morphological changes induced by T3 treatment in trβ crispants

Fig. 8. Compared mobilities of passenger proteins in G2/M-prophase, metaphase and anaphase.FRAP experiments were performed on HeLa cells stably expressing.

Fig. 3. Mean force and velocity during jumping

Leeches require closed loop sensory feedback to localize stimuli.

Fig. 4. Representative still images of behaviour and characteristics typical of inshore foraging strategy of Australasian gannets. Representative still.

Table 1. Measurement of ring diameters of proteins localizing in ring-like patterns around centrioles.Consideration of the size of IgG (about 8 nm) raises.

Fig. 5. Behaviours of the wild-types Oregon-R at two temperatures.

Fig. 6. ERGs recorded to UV stimuli at 330 nm, 350 nm and 370 nm to increasing (top to bottom) stimulus intensity. ERGs recorded to UV stimuli at 330 nm,

Fig. 3. Changes in the total EPS/Chl a ratio and bend interval of trichomes before and after the removal of polysaccharide from the BG11-cultured N. flagelliforme.

Fig. 1. lgl interacts genetically with Argonaute 1 (AGO1) in the eye.

Fig. 8. Expression of other genomic-clustered Chrn subunits in the mesodiencephalon.(A) Schematic representation illustrating the assembly of the Chrnb4,

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Fig. 4. Spectra of monochromatic light from the OLS Fig. 4. Spectra of monochromatic light from the OLS. Spectra were measured separately at λ=700, 750, 800, 850, and 900 nm using a spectroradiometer (S-2440C; Soma Optics, Tokyo, Japan), but were illustrated together in this figure as black lines. Spectra of monochromatic light from the OLS. Spectra were measured separately at λ=700, 750, 800, 850, and 900 nm using a spectroradiometer (S-2440C; Soma Optics, Tokyo, Japan), but were illustrated together in this figure as black lines. The difference in intensity (see Table 2) reflected the spectrum of the light source, which was a xenon arc lamp (Watanabe et al., 1982). The gray line indicates the spectrum of light from red LED lamps (VBL-S300-R; Valore, Kyoto, Japan), with a peak wavelength at 660 nm. Megumi Matsuo et al. Biology Open 2018;7:bio033175 © 2018. Published by The Company of Biologists Ltd