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

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카탈로그 번호 AMAFD1000
제품 가격(KRW)
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The EVOS FL Auto Imaging System is a fully-automated, digital, inverted multi-channel fluorescence and transmitted light imaging system with outstanding workflow efficiency. Designed to meet demanding requirements over a broad range of applications, the EVOS FL Auto system supports high-resolution mosaic tiling, multi-position well scanning, cell counting with thresholding, and time-lapse studies. The intuitive interface, proprietary light cubes, dual cameras, precision automated stage and parfocal optical system enables you to produce publication quality images in seconds.

The EVOS FL Auto Imaging System offers you these important advantages:

• Exceptional ease-of-use with a fully automated and motorized X/Y scanning stage, autofocus and flat-focus Z-stack
• Advanced software featuring high-resolution mosaic tiling, multi-position well scanning, object counting, and time-lapse
• Outstanding versatility with a 5-position objective turret, 4-color fluorescence, plus color and B/W cameras
• 22" touch-screen LCD display, networking capability, and DVI output

Compare cell imaging systems >

Software downloads for the EVOS FL Auto Imaging System >

Fully Automated Imaging System
The EVOS FL Auto system combines and integrates precision components with a unique design functionality that enables high-quality automated fluorescence imaging with superior work-flow efficiency. Full automation of the precision X/Y-stage movement; automated changes of up to 4 LED fluorescence light cubes and 5 parfocal objectives, focus, and exposure; and dual camera switching makes the EVOS FL Auto system an exceptional platform for a variety of demanding imaging applications. Program the EVOS FL Auto system to run acquisition routines, 8-point time lapse experiments, and tile-stitch scans in nearly any vessel through the sensitive touch-screen display.

Versatile and Highly Configurable
With a 5-position objective turret and 4 fluorescence light cube positions, the optical system can be easily configured to meet your needs. Choose from our full range of high-quality objectives from 2x to 100x magnification, and over a dozen LED light cubes. The EVOS FL Auto system automatically adjusts the lighting settings to match the objective magnification. Dual cameras with a Sony ICX445 CCD monochrome and a high sensitivity CMOS color digital camera enable seamless imaging of both fluorescent and colorimetrically stained samples. Interchangeable stage plates and vessel holders accommodate most vessel types and sizes, including multi-well plates, slides, culture flasks, and Petri dishes, and afford precise control and sample alignment by the automated stage.

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.

Fully Integrated Environmental Control Sy
For Research Use Only. Not for use in diagnostic procedures.
사양
ColorTransmitted Light
Data OutputBMP Files,JPG Files,PNG Files,TIFF Files
Detection MethodChromogenic,Colorimetric,Fluorescent
Dimensions34 cm (14 in) (W) x 32 cm (13 in) (H) x 47 cm (19 in) (D)
Display Interface22-inch color
For Use With (Equipment)Fluorescence Microscope
FormatSpecific Holder Attachments
Frequency50⁄60 Hz
Input Voltage100-240 VAC
Objectives5 Objective Turret
Product LineEVOS®
Product Size1 each
StageMotorized encoded X/Y scanning stage with sub-micron resolution
Weight20 kg (44.1 lbs)
Unit Size1 each
구성 및 보관
Unit includes:

EVOS Auto FL Imaging System
22" multi-touch monitor
External PC with 16 GB RAM
FL Auto Accessory Kit
  3 US power cords*
  Condenser Slider, Diffusion
  Condenser Slider, Block
  Vessel Holder, slides (AMEPVH001)
  Vessel Holder/Adapter, multi-well plates (AMEPVH022)
  Light shield
  Dust cover
  USB A to B cable (6')/DVI cable (6')
  USB stick
  Cartridge extraction tool
  Corded optical USB mouse
  Light cube access door
  EVOS Calibration Slide (AMEP4720)

*Note that a country-specific power cord must be ordered separately in regions not using the Type A power plug.

자주 묻는 질문(FAQ)

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.

Can the EVOS cell imaging systems be used to automatically count cells?

Only the EVOS FL Auto Imaging System and EVOS FL Auto 2 Imaging System have an automatic cell counting function. On the EVOS FL Auto Imaging System, automatic cell counting is enabled via built-in instrument firmware whereas on the EVOS FL Auto 2 Imaging System, the Celleste Image Analysis Software needs to be purchased separately to enable automatic cell counting.

The EVOS XL, EVOS FL, and EVOS FL Color imaging systems provide a manual cell counting tool that allows tagging of up to six different labels on the screen image.

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

What is the difference between the FLoid Cell Imaging Station and the EVOS FL imaging systems?

The FLoid Cell Imaging Station is a simple, easy-to-use transmitted-light and three-color fluorescence microscope. The three fluorescent colors, blue, green, and visible red (Texas Red dye) are set and cannot be changed to other filter sets. The magnification is also set with a 20x objective; this objective cannot be removed or changed.

On the other hand, the EVOS FL Imaging Systems are easy-to-use transmitted-light and fluorescence microscopes that allow the user access to the objective turret and light cube tray to permit multiple options for magnification and fluorescence detection. The EVOS FL Imaging Systems allow the use of 23 different light cubes and 18 different objectives (from 2x to 100x).

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

인용 및 참조 문헌 (20)

인용 및 참조 문헌
Abstract
Astrocyte-Microglia Cross Talk through Complement Activation Modulates Amyloid Pathology in Mouse Models of Alzheimer's Disease.
Authors:Lian H, Litvinchuk A, Chiang AC, Aithmitti N, Jankowsky JL, Zheng H,
Journal:J Neurosci
PubMed ID:26758846
'Increasing evidence supports a role of neuroinflammation in the pathogenesis of Alzheimer''s disease (AD). Previously, we identified a neuron-glia signaling pathway whereby Aß acts as an upstream activator of astroglial nuclear factor kappa B (NF-?B), leading to the release of complement C3, which acts on the neuronal C3a receptor (C3aR) ... More
Expression and characterization of three Aurora kinase C splice variants found in human oocytes.
Authors:Fellmeth JE, Gordon D, Robins CE, Scott RT, Treff NR, Schindler K,
Journal:
PubMed ID:25995441
'Chromosome segregation is an extensively choreographed process yet errors still occur frequently in female meiosis, leading to implantation failure, miscarriage or offspring with developmental disorders. Aurora kinase C (AURKC) is a component of the chromosome passenger complex and is highly expressed in gametes. Studies in mouse oocytes indicate that AURKC ... More
Selenocysteine derivative overcomes TRAIL resistance in melanoma cells: evidence for ROS-dependent synergism and signaling crosstalk.
Authors:Cao W, Li X, Zheng S, Zheng W, Wong YS, Chen T,
Journal:
PubMed ID:25277183
'Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL), as one of the most promising targeted drug for new cancer therapeutics, is limited in clinical application by the evolution of resistance in many cancer cell lines, especially in malignant melanoma. Thus, it is urgently needed to identify chemosensitizers to enhance the apoptotic inducing ... More
Pancreatic Cancer Stem-like Cells Display Aggressive Behavior Mediated via Activation of FoxQ1.
Authors:Bao B, Azmi AS, Aboukameel A, Ahmad A, Bolling-Fischer A, Sethi S, Ali S, Li Y, Kong D, Banerjee S, Back J, Sarkar FH,
Journal:
PubMed ID:24719318
'Subpopulations of cancer stem cells (CSCs) or cancer stem-like cells (CSLCs) have been identified from most tumors, including pancreatic cancer (PC), and the existence of these cells is clinically relevant. Emerging evidence suggests that CSLCs participate in cell growth/proliferation, migration/invasion, metastasis, and chemo-radiotherapy resistance, ultimately contributing to poor clinical outcome. ... More
Oncogenic signaling in amphiregulin and EGFR-expressing PTEN-null human breast cancer.
Authors:Kappler CS, Guest ST, Irish JC, Garrett-Mayer E, Kratche Z, Wilson RC, Ethier SP,
Journal:
PubMed ID:25454348
A subset of triple negative breast cancer (TNBC) is characterized by overexpression of the epidermal growth factor receptor (EGFR) and loss of PTEN, and patients with these determinants have a poor prognosis. We used cell line models of EGFR-positive/PTEN null TNBC to elucidate the signaling networks that drive the malignant ... More