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30 protocols using eos 5d

1

Time-Lapse Capture of Flower Closure

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The closure of I. purpurea flowers was captured by photographing the flowers horizontally using a Canon EOS5D digital camera (Canon Inc., Tokyo, Japan). For movie scanning, images of flower closure were taken with a Canon EOS5D camera once per minute, and Premier Pro CS6 software (Adobe Systems Incorporated, United States) was used to generate a video.
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2

Visualizing ROS Accumulation in Plants

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The accumulation was visualized by nitroblue tetrazolium (NBT) staining. Leaf disks (1.5 cm in diameter) were directly infiltrated with 0.1 mg ml-1 NBT in 25 mM K-HEPES buffer (pH7.8) and incubated at 25°C in the dark for 4 h. Then, the leaf disks were rinsed in 95% (v/v) ethanol for 10 min at 95°C and photographed with a digital camera (Canon EOS 5D; Canon Inc., Tokyo, Japan).
For the histochemical staining of H2O2, leaves were detached and placed in a solution containing 1 mg ml-1 3,3′-diaminobenzidine (DAB, pH 5.5) for 6 h after a light vacuum infiltration. Leaf disks were boiled in 95% (v/v) ethanol for 10 min, stored in 50% glycerol, and then photographed with a digital camera (Canon EOS 5D; Canon Inc., Tokyo, Japan) or an Olympus motorized system microscope (BX61, Olympus Co., Tokyo, Japan) at 400 magnifications (Thordal-Christensen et al., 1997 (link)).
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3

Zymographic Analysis of MMP Activity

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Metalloproteinase activity was determined by zymography. Supernatant of culture from DC/TL treated or not with LMW HA was run on a 10% SDS PAGE containing 0.1% gelatin (Sigma-Aldrich). The gel was stained with Coomassie Brilliant Blue R-250 for 30 min at room temperature. gelatinase activity was visualized by negative staining; gel images were obtained with a digital camera (Canon EOS 5D), and were subjected to densitometric analysis using Scion Image software (Scion Corporation, Frederick, MD). Relative MMP-2 activity was obtained by normalizing values to untreated samples (DC/TL). HT1080 cell line supernatant was used as positive control of MMP-2 and MMP-9 activity [30] (link).
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4

Multimodal Oral Cancer Screening

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First, a senior specialist dentist collected personal information and performed COE on the subjects and then took color photographs of the lesions with a Canon camera EOS 5D under white light. VELscope® was used to perform autofluorescence examination of the patients under dim indoor light; fluorescence photos were taken, and suspicious sites were identified. Both the patients and the examiner wore protective goggles during the entire process. Then, objective VELscope fluorescence examination with quantitative analysis was performed. Based on the results of COE and fluorescence examination, a biopsy was performed for all lesions by a senior specialist dentist with 20 years of clinical experience in treating mucosal diseases and oral cancer. The samples were stained with routine hematoxylin and eosin for morphological diagnosis by an experienced oral pathologist. The pathologist was blinded to the clinical examination results of the VELscope®. Finally, the research results were statistically analyzed and discussed.
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5

Multimodal Characterization of MME Structures

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The morphology and corresponding elemental mapping images of MME structures were measured using scanning electron microscopy (Quanta 400 F, FEI, USA) and its energy dispersive spectroscopy (EDS), respectively. NdFeB microparticles and liquid metal distribution inside the MME structure were measured by micro-CT (GE Vtomex). The optical photos of the MME structure were captured by the digital SLR camera (EOS5D, Canon, Japan). The morphology of the MME structure was measured by the ultra-depth three-dimensional microscope (VHX-7000, KEYENCE, Japan).
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6

Characterization of Magneto-Origami Actuators

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The surface topography of dual-layer magnetic paper was observed using an industrial digital camera (CM2000, KUY NICE, China). The magnetic flux density of magneto-origami was measured by a gauss meter (Shanghai Daxue Electromagnetic Equipment Co., Ltd., China). The contractions strain and folding angle of magneto-origami actuators were characterized by analyzing the Supplementary Movies recorded by a digital camera (EOS 5D, Canon, Japan) using Image J. The magnetic hysteresis loop of bilayer matter was obtained using a vibrating sample magnetometer (VSM, Lake Shore 7410, USA).
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7

Periocular Image Evaluation Protocol

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For the evaluation of proposed work, raw input images from publicly available UBIPr periocular database created by Padole and Proenca [20 ] is used. This database contains total 10252 images represented in RGB color space in .bmp format. Images were captured using CANON EOS 5D digital Camera in highly controlled lab conditions and setups such as four meter to eight meter in steps of one meter distance variation, different illumination, frontal, 30 and -30 degree pose variation and occlusion variability. To create metadata of images, researchers were manually annotated the images for iris center, canthus points and inner, outer, mid points of eyebrow. Annotations also included information about gaze angle, gender, pigmentation level, eye closure and presence of glasses. Sample images from UBIPr database is shown in Fig. 3.

Sample Images from UBIPr Database

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8

Astrodia Specimen Collection and Preservation

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Five specimens of Astrodia were collected by ROV HAILONG III, ROV HAILONG IV, and HOV JIAOLONG, from seamounts in the Philippine Sea and the Northwest Pacific, during several COMRA’s cruises in 2013, 2020, and 2021 (Fig. 1). All specimens were preserved in 95% ethanol on board the vessels and photographed using a digital camera (Canon EOS 5D), then deposited in the repository of the Second Institute of Oceanography, Hangzhou, China (RSIO).
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9

Imaging Drosophila Developmental Stages

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Photos of early embryos were taken with a Zeiss Lumar V12 fluorescence stereomicroscope equipped with NA objective (ApoLumar S1.2X) and AxioCam MRm camera. Images were taken using Zeiss AxioVision 4.8.2 software. The contrast of the TIFF images was adjusted with Adobe Photoshop. Photos of adult flies, larva, and pupa were taken with a Zeiss Stemi SV11 stereomicroscope equipped with NA objective (S 1.0X) and Canon EOS 5D camera (attached to the binocular the tube via Gosky T2 camera mount; 23.2 mm eyepiece port). The contrast of raw images was adjusted with Adobe Photoshop. The size standard was photographed separately in the same condition and the image was merged with Photoshop. No filters are used for any photos. Standard light (halogen gooseneck lamp) was used for both microscopes.
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10

Underwater ROV Survey of Hydrothermal Structures

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A fine scale ROV survey, covering the area mapped by the multibeam (Fig 2), was carried out to classify and characterize the hydrothermal structures and the associated fauna. The Pollux III ROV was equipped with a high resolution camera (Canon EOS 5D, 20 megapixel), two strobes (Canon), a high definition video camera (Sony HDR-HC7), 3 jaw grabbers, two parallel laser pointers to measure in situ seafloor structures and a USBL (Ultra Short Baseline—TrackLink 1500 MA Link Quest Inc.) underwater acoustic position system to accurately record the ROV’s geographic position. The main hydrothermal structures were identified and mapped. A small basket net was installed on the ROV to collect samples of terminal parts of chimneys. Samples of a total of three chimneys were collected, named VA (Chimney_VAlentina, 38°39’27”N, 15°6’1”E), SF (Chimney_Sagrada Familia, 38°39’25”N, 15°6’0”E), and GB (Chimney_Giovanni Bortoluzzi, 38°39’23”N, 15°5’57”E) (Fig 3B). In addition, a fourth chimney (RC, Chimney_ReConstructed, 38°39’30”N, 15°6’3”E) (Fig 3B) was reconstructed by means of a mosaic of 250 HD-video images processed with the Software Agisoft PhotoScan (www.agisoft.com) in order to provide a graphical representation of the investigated chimneys allowing a better understanding of the size and shape of the entire structure of the chimney.
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