The largest database of trusted experimental protocols

Ve 7800

Manufactured by Keyence
Sourced in Japan

The VE-7800 is a high-resolution digital microscope designed for laboratory applications. It features a 2-megapixel camera and the ability to capture images and videos. The VE-7800 provides magnification capabilities from 10x to 1000x.

Automatically generated - may contain errors

24 protocols using ve 7800

1

Scanning Electron Microscopy of Fly Eyes

Check if the same lab product or an alternative is used in the 5 most similar protocols
Adult flies were anesthetized, mounted on stages and observed with a VE-7800 (Keyence Inc.) scanning electron microscope. In every experiment, at least five adult flies of each line were chosen for scanning electron microscopy observation to assess the eye phenotype, and these experiments were repeated three times. In the experiments, no significant variation in eye phenotype among the five individuals was observed.
+ Open protocol
+ Expand
2

SEM Visualization of Leaf Epidermal Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
For SEM (VE-7800; Keyence, Tokyo, Japan) observations, fresh leaves of the Empire and Salinas type were collected and mounted on a pedestal with carbon tape. The epidermal cells of leaf surface was visualized using SEM.
+ Open protocol
+ Expand
3

Optical Vortex Beam Irradiation on Silicon

Check if the same lab product or an alternative is used in the 5 most similar protocols
Figure 1 shows the experimental setup for the irradiation of an optical vortex beam on a Si target. A Q-switched Nd:YAG laser (Spectra Physics, Quanta-Ray, LAB-150) with a wavelength of 1064 nm and a pulse duration of 17 ns was used as the ablation laser. A linearly polarized Gaussian beam from the laser was converted into a circularly optical vortex beam through the vortex phase plate with  =  − 1 and the quarter wave plate (QWP), as shown in Fig. 1. A single pulse of the doughnut beam was focused by a plano-convex lens (f = 50 mm) on the surface of the Si target. The irradiation spot size and laser fluence are key factors for the droplet ejection. Thus, in this experiment, the spot size was changed by increasing the distance between the Si target and the focus lens from the focal point (z = 0 µm) to z = 600 µm at 100 µm intervals. The pulse energy was fixed at 0.08 mJ. The irradiated surface was observed by a scanning electron microscope (KEYENCE, VE7800). The ablated structures were gradually increased with defocusing, as shown in Fig. 1. Cone structures were formed at the center of the irradiation spots at z = 0–400 µm.
+ Open protocol
+ Expand
4

Charpy Impact Behavior of Steel Bars

Check if the same lab product or an alternative is used in the 5 most similar protocols
The appearance of the samples after the Charpy test was taken through a digital microscope, VHX-900 (Keyence corporation, Osaka, Japan), and digital camera. The microstructures were observed through a scanning electron microscope (SEM), VE-7800 (Keyence Corporation, Osaka, Japan), operated at 15 kV. The electron backscattered diffraction analysis was conducted using a 7001F (JEOL, Tokyo, Japan) equipped with a TSL-OIM analytical system.
For each steel bar, full-size 2 mm V-notched specimens with a notch radius of 0.25 mm were machined along the RD, as shown in Figure 3b, and instrumented Charpy impact tests were conducted under a 500 J capacity using CIEM-500D (Tokyo Koki Testing Machine Co., LTD., Sagamihara, Japan). The P and u during the impact test were recorded every 2.0 μs. The value of DBTT was determined from the Charpy curve, i.e., DBTT denoted the absorbed energy transition temperature corresponding to the half value of the vEu.
+ Open protocol
+ Expand
5

Electrospun Silk Fibroin/Polyurethane Composite Evaluation

Check if the same lab product or an alternative is used in the 5 most similar protocols
A porous structure is desirable for cell and tissue immigration and the growth of tissue engineering materials because the extracellular matrix (ECM) of native tissue has a similar structure [19 (link)]. The electrospun SF/PU composite patches were evaluated by gross observation and their morphology was characterized using a SEM operated at 10 kV with a 1000× magnification (VE-7800 Keyence Co., Osaka, Japan). The obtained image was analyzed and the fiber diameter was determined by randomly selecting 50 fibers from each image.
+ Open protocol
+ Expand
6

Preparation and Observation of Egg White Gels

Check if the same lab product or an alternative is used in the 5 most similar protocols
Egg white gels were sliced from the inside with a razor (FH‐10; Feather Safety Razor Co., Ltd., Osaka, Japan) into pieces of about 5 × 5 × 5 mm. Samples were fixed in 3% glutaraldehyde in 88 mM phosphate buffer (pH 7.4) at 4C for 3 days, washed in 100 mM phosphate buffer (pH 7.4) and dehydrated by passing through graded ethyl alcohol solutions (50–100%). Then, samples were treated with t‐butanol (50–100%), dried in a centrifugal concentrator (VC‐360; Taitec Co., Ltd., Saitama, Japan), mounted on aluminum stubs (OP‐51436; Keyence Corporation, Osaka, Japan) with carbon double‐sided tape (Nisshin EM Corporation, Tokyo, Japan), and coated with gold using Quick Coater (SC‐701; Sanyu Electron Co., Ltd., Tokyo, Japan). The samples were observed under an SE microscope (VE‐7800; Keyence Corporation, Osaka, Japan) at 20 kV.
+ Open protocol
+ Expand
7

Scanning Electron Microscopy of Fly Eyes

Check if the same lab product or an alternative is used in the 5 most similar protocols
Adult flies were anesthetized, mounted and inspected under a scanning electron microscope (Keyence VE-7800) in high vacuum mode and stereomicroscope (Olympus SZX-ILLB100). In every experiment, the eye phenotypes of at least five newly eclosed adult male flies of each line were simultaneously examined by scanning electron microscope and stereomicroscope. Three independent experiments for each line were carried out and no significant variation in the compound eye phenotype was observed among individuals.
+ Open protocol
+ Expand
8

Scanning Electron Microscopy of Fly Eyes

Check if the same lab product or an alternative is used in the 5 most similar protocols
Adult flies were anesthetized, mounted on stages and observed with a VE-7800 (Keyence Inc.) scanning electron microscope or JSM-6510A (JEOL) analytical scanning electron microscope. In every experiment, at least five adult flies of each line were chosen for scanning electron microscopy observation to assess the eye phenotype, and these experiments were repeated 3 times. In the experiments, no significant variation in eye phenotype among the five individuals was observed.
+ Open protocol
+ Expand
9

SEM Imaging of Glutaraldehyde-Fixed Tissues

Check if the same lab product or an alternative is used in the 5 most similar protocols
PPs were excised and fixed for 2.5 hours with 2.5% glutaraldehyde in 0.1 M phosphate buffer (pH7.4). The tissues were completely dehydrated in a graded ethanol series. Specimens were coated with a gold layer using a sputter coater MSP-1S (Shinku Device) and observed by SEM (VE-7800, KEYENCE).
+ Open protocol
+ Expand
10

Silk Fibroin Sponge Fabrication

Check if the same lab product or an alternative is used in the 5 most similar protocols
Silk fibers were obtained from Bombyx mori cocoons and degummed as previously described [25 (link)]. Briefly, silk fibers were obtained by reeling and weaving silk cocoons in boiled water at 80 °C for about 15 min. The dried silk threads were placed in a mixture of sodium carbonate (0.08%, w/v) and Marseille soap (0.12%, w/v) at 95 °C for 120 min. This process was repeated to completely remove the silk sericin from the raw silk fibers. The removal of silk sericin was confirmed using a SEM (VE-7800, Keyence Co., Osaka, Japan). Degummed SF fibers were dissolved in 9 M lithium bromide (LiBr) solution at a concentration of 10% (w/v) at 37 °C for 3 h. Then this solution was dialyzed against distilled water until LiBr was completely removed. The SF aqueous solution was obtained by purification of the dialyzed solution by centrifugation. The final concentration of the SF aqueous solution was approximately 4% (w/v). To obtain SF sponge, SF aqueous solution was diluted to 1% (w/v) and then freeze-dried over 24 h.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!