You won’t actually see the dust mites that share your home, because they’re vanishingly small (a family of mites could pack themselves into the period at the end of this sentence). But if you looked at one under a microscope, you’d see an otherworldly, eight-legged creature. ...
The wavelength of the excitation laser, which is focused onto the sample solution via a high numerical aperture microscope objective, should be considered carefully according to the characteristics of the sample. The scattered Raman signals are dispersed using a spectrograph and a detector is employed...
Mouse ears were harvested and split into halves. After fixation in 4% paraformaldehyde in PBS for 1 h on ice, the tissues were washed in PBS at 4 °C for 1 h. The subcutaneous cartilage was carefully removed with tweezers under a stereo microscope. The remaining tissues were blocked...
Cutibacterium acnes(C. acnes) which dominate the upper 1.2–1.9 mm of terminal of pilosebaceous units7,8,9.Cutibacterium acneshelp to preserve and support the natural microbial balance of the skin, however, under certain conditions it can also substantially alter its...
Under a Creative Commons license open accessMacrophages can be polarized into two subsets: a proinflammatory (M1) or an anti-inflammatory (M2) phenotype. In this study, we show that an increased M1-to-M2 ratio associated with a decrease in IL-34 induces skin inflammaging. The total number of...
In order to study the effects of foliar micronutrient application under water stress at three stages of growth on proline and carbohydrate concentrations, ... M Babaeian,A Tavassoli,A Ghanbari,... - 《Journal of Science & Technology of Agriculture & Natural Resources》 被引量: 51发表: 2009年...
(A) tSNE plot for all epithelial cells from UW skin with cell each type indicated. The percentage of cells in each cluster per total number (7,099) of cells under analysis is indicated in parenthesis. (B) tSNE plot for all epithelial cells (4,021) from WO skin. (C) Bar graph repres...
Sections with 4 µm of thickness were prepared by a microtome and mounted on poly-L-lysine-coated slides for H&E staining. We calculated the number of microvessels per unit area (/mm2) under a light microscope (×200 magnification, Olympus Corp, Tokyo, Japan), which indicated the ...
The microstructure and morphology of SFSHs were observed by scanning electron microscope (SEM). As observed in Fig. 2H and Supplementary Fig. 2, both SFSHs and the control polyacrylamide hydrogel after lyophilization exhibited a porous 3-dimentional (3D) structure under a low magnification. With ...
The sections were mounted and photographed under a confocal microscope (ZEISS). The primary antibodies were rabbit anti-GPR39 (NLS139, NOVUS), rabbit anti-GPR39 (NLS142, NOVUS), goat anti-Blimp1 (ab13700, Abcam) and goat anti-Lrig1 (AF3688, R&D Systems) antibodies. The secondary ...