EVOS™ FL Imaging System
EVOS™ FL Imaging System
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EVOS™ FL Imaging System

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카탈로그 번호 AMF4300
제품 가격(KRW)
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The EVOS FL Imaging System is a fully integrated, digital, inverted imaging system for four-color fluorescence and transmitted-light applications. It is powerful, yet easy-to-use and delivers high-definition images with exceptional convenience. The unique light cubes, sensitive camera, and precision-engineered optical system make the EVOS FL system ideal for both demanding and routine fluorescence imaging applications.

The EVOS FL Imaging System offers you these important advantages:

• Easy installation; no maintenance, assembly, alignment, or calibration
• For four-color fluorescence and transmitted light applications
• Five-position objective turret with front controls
• On-board software
• All-in-one design: digital camera, precision optics, LCD display, and USB storage

Fully Integrated Imaging System
The EVOS FL system represents a new concept in transmitted light inverted microscopy. It is a fully integrated imaging system that combines precision optics, a 15" high-resolution LCD display, and a highly sensitive Sony ICX445 monochrome CCD camera (1280 x 960 pixel resolution, 1.3 Megapixels). Images are seamlessly acquired through the intuitive user interface using a mouse for easy control. Monochrome cameras are commonly used for high-performance fluorescence applications and provide the best sensitivity for detection of faint fluorescence signals. Color cameras, as on the EVOS FL Color System, have lower fluorescence sensitivity but have the advantage of being able to differentiate structures by color in transmitted light (e.g., imaging stained tissue samples).

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Versatile and Highly Configurable
The EVOS FL system features an easily accessible 5-position objective turret and a 3-position condenser turret. The 4 fluorescence light cubes are lever-actioned for rapid and easy selection. The optical system can be configured to best meet your needs using our full range of high-quality objectives from 2x to 100x magnification. Lighting settings are automatically adjusted to match the objective magnification. The EVOS FL system features a mechanical stage with X/Y-axis fine-positioning using control knobs conveniently located on the left side and the front of the stage. The stage accommodates EVOS vessel holders that provide a perfect fit for most vessel types and sizes. Interchangeable stage plates accommodate most vessel types and sizes, including flasks, Petri dishes, multi-well plates, and slides.

Smart LED Illumination Technology
All EVOS fluorescence imaging systems utilize our unique, proprietary LED light cubes. This world-leading light engine outputs remarkable intensity over a short light-path that delivers superior fluorophore excitation. Each light cube contains a precisely matched set of optical components to optimize the position, evenness, and intensity of the light beam. Digitally controlled LED light sources allow adjustment of illumination levels, dramatically improving control over photobleaching. Hard-coated filters give sharper edges and significantly higher transmission efficiencies than traditional soft-coated filters.

Integrated Software
The on-board computer makes the EVOS FL system easy to run and use, and the intuitive, comprehensive software facilitates both image acquisition and analysis. Modules include time-lapse acquisition, manual-assist cell counting, and image review. Saved user settings work in conju
For Research Use Only. Not for use in diagnostic procedures.
사양
ColorTransmitted Light
Data OutputBMP Files,JPG Files,PNG Files,TIFF Files
Detection MethodFluorescent
Dimensions36 cm (14 in) (W) x 58 cm (23 in) (H) x 47 cm (19 in) (D)
Display Interface15-inch color monitor,Adjustable tilt
For Use With (Equipment)Fluorescence Microscope
FormatSpecific Holder Attachments
Frequency50⁄60 Hz
Input Voltage100-240 VAC
Objectives5 Objective Turret
Product LineEVOS®
Product Size1 each
StageMechanical stage with X-Y axis fine-positioning controls
Weight15.3 kg (33.7 lbs)
Unit Size1 each
구성 및 보관
Unit includes:

EVOS FL Imaging System
Power adapter*
Universal stage plate
USB optical mouse
Dust cover
USB flash drive (includes User Guide and Quick Start Guide)
Diffusion Condenser Slider
Condenser Slider Block
UV shield/light shield
Light cube access door
Stage lock pin (in place on stage)

*Note that a country-specific power cord must be ordered separately.

자주 묻는 질문(FAQ)

Images captured with our EVOS FL Cell Imaging System are dimmer than when the sample is viewed live through the camera. Would you suggest any fixes for this problem?

With the EVOS FL Cell Imaging System (and the EVOS FL Color Imaging System), there is a ''live'' mode which shows the field of view live while you orient your sample. When you are imaging in ''live'' mode, the system increases the gain setting so it can have a quicker refresh rate. (Note: The EVOS FL doesn't allow manual adjustments of the gain setting). This makes it easier to move around the sample to orient yourself and see your sample without having long pauses due to longer exposure time. This also helps to reduce photobleaching. With a higher gain, you have a lower exposure time (but you also have higher background).

You will then capture the image with either ''Find and Focus'' mode or ''Actual'' mode. If using ''Find and Focus'' mode, when you capture the final image, the system will reset the exposure time and gain setting to optimize the contrast for your sample, which may be different than what you see in ''live'' mode. You can only adjust the light intensity in ''Find and Focus'' mode. ''Find and Focus'' mode is often best for qualitative imaging. If this is not conducive for your assay, or if you are performing quantitative assays that require more normalization across samples, then you will want to use ''Actual'' mode where you can control the exposure time yourself as well as the light intensity.

Find additional tips, troubleshooting help, and resources within our Cell Imaging Support Center.

Where is the serial number on the EVOS FL Imaging System (Cat. No. AMF4300) located?

The serial number on the EVOS FL Imaging System can be found in two places.
- The first place is a sticker on the "neck" under the monitor. You have to tilt the monitor backward to see it.
- The second place is in the software. When the instrument is booted up, click on Settings ("gear" icon at bottom of screen). The serial number can be found at the top of the "Basic" tab.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

I'm trying to acquire an image on the EVOS imaging system, but nothing shows up on the monitor. What can be causing this?

For the EVOS imaging systems:

Make certain the light is on (easy way to test this: place a piece of thin paper on the stage).
Make certain the sample is not too opaque; compare with a calibration slide or another, thinner or single-cell sample on a slide.
Check the objectives to make certain the turret is in alignment and the objective is completely threaded in its slot.
For the EVOS FL Imaging System: change the position of the light cubes.
For the EVOS FL Auto Imaging System: check the insertion of all USB ports for connectively from scope to computer.
For brightfield settings, check the condenser slider slot; make certain the condenser sliders are completely in place.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

I'm using an EVOS imaging system and my objective is rubbing up against the edge of the vessel holder of my stage. How can I correct this?

Objectives can hit the vessel holder when they are focused too high in the Z axis (up and down). This is a particularly a problem with the EVOS FL Auto Imaging System during instrument start-up, when the stage moves during system initiation, or when changing objectives. Coverslip-corrected objectives tend to be wider and flatter at the top of the barrel, which means that they are more likely to run into the edges of the vessel holder, particularly if you are imaging at the edges of the sample container. In those cases, use of that objective for those areas of the container may not be possible. If the objective if “jammed” by the vessel holder, then carefully unscrew the thumbscrews of the vessel holder and lift it straight off the stage, then move the objective downward in focus and toward the center of the stage. It is a good idea to have a shut-down procedure in your lab that includes moving the objectives to the lowest magnification and focusing downward with course focus prior to turning off the instrument for the day.
An objective can be damaged by scraping against the vessel holder. If this happens, take out the objective and examine it carefully for damage, particularly on the lens.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

I want to check to make sure I have the most up-to-date software for my EVOS imaging system. Where do I go for this?

Here is a page you can go to - https://www.thermofisher.com/us/en/home/products-and-services/services/instrument-qualification-services/instruments-and-services-portal/instrument-software-downloads.html. Look under the “Cell Imaging Systems” section and follow the link for your EVOS imaging system. There you will find the free download link as well as instructions to follow. We recommend you check for updates at least every six months, or if your system seems to have a software glitch of any sort.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

인용 및 참조 문헌 (108)

인용 및 참조 문헌
Abstract
Heparan sulfate facilitates Rift Valley fever virus entry into the cell.
Authors:de Boer SM, Kortekaas J, de Haan CA, Rottier PJ, Moormann RJ, Bosch BJ,
Journal:J Virol
PubMed ID:23015725
Rift Valley fever virus (RVFV), an emerging arthropod-borne pathogen, has a broad host and cell tropism. Here we report that the glycosaminoglycan heparan sulfate, abundantly present on the surface of most animal cells, is required for efficient entry of RVFV. Entry was significantly reduced by preincubating the virus inoculum with ... More
Pseudogout-associated inflammatory calcium pyrophosphate dihydrate microcrystals induce formation of neutrophil extracellular traps.
Authors:Pang L, Hayes CP, Buac K, Yoo DG, Rada B,
Journal:
PubMed ID:23677474
'Pseudogout is an autoinflammatory condition triggered by calcium pyrophosphate dehydrate (CPPD) crystal deposition in the joints. The innate immune system is irritated by and responds to the presence of the crystals with an inflammatory response. The synovial fluid contains activated inflammatory macrophages and neutrophil granulocytes. Several details of crystal-induced macrophage ... More
Preclinical activity profile and therapeutic efficacy of the HSP90 inhibitor ganetespib in triple-negative breast cancer.
Authors:Proia DA, Zhang C, Sequeira M, Jimenez JP, He S, Spector N, Shapiro GI, Tolaney S, Nagai M, Acquaviva J, Smith DL, Sang J, Bates RC, El-Hariry I,
Journal:
PubMed ID:24173541
'Treatment options for patients with triple-negative breast cancer (TNBC) are largely limited to systemic chemotherapies, which have shown disappointing efficacy in the metastatic setting. Here, we undertook a comprehensive evaluation of the activity of ganetespib, a potent inhibitor of HSP90, in this malignancy. The antitumor and antimetastatic activity of ganetespib ... More
Secreted meningeal chemokines, but not VEGFA, modulate the migratory properties of medulloblastoma cells.
Authors:Davare MA, Lal S, Peckham JL, Prajapati SI, Gultekin SH, Rubin BP, Keller C,
Journal:
PubMed ID:24928387
'Leptomeningeal metastasis is a cause of morbidity and mortality in medulloblastoma, but the understanding of molecular mechanisms driving this process is nascent. In this study, we examined the secretory chemokine profile of medulloblastoma cells (DAOY) and a meningothelial cell line (BMEN1). Conditioned media (CM) of meningothelial cells increased adhesion, spreading ... More
Hepatitis C virus core protein inhibits interferon production by a human plasmacytoid dendritic cell line and dysregulates interferon regulatory factor-7 and signal transducer and activator of transcription (STAT) 1 protein expression.
Authors:Stone AE, Mitchell A, Brownell J, Miklin DJ, Golden-Mason L, Polyak SJ, Gale MJ, Rosen HR,
Journal:
PubMed ID:24788809
'Plasmacytoid Dendritic Cells (pDCs) represent a key immune cell population in the defense against viruses. pDCs detect viral pathogen associated molecular patterns (PAMPs) through pattern recognition receptors (PRR). PRR/PAMP interactions trigger signaling events that induce interferon (IFN) production to initiate local and systemic responses. pDCs produce Type I and Type ... More