Evolve® EMCCD cameras
Evolve® 512 Delta EMCCD Camera
Unprecedented speed and sensitivity for super resolution applications
Discover a new way to evolve your science with the fastest and most productive EMCCD camera available in the world. The Evolve 512 Delta empowers you with the potential to obtain research results in about half the time of previous 512 EMCCD cameras. Designed specifically for demanding Super-Resolution applications, this camera delivers an unprecedented new level of speed and sensitivity.
- 20MHz 512x512 EMCCD
- 67 Frames per Second.
- 72e- Read Noise, <1e- Using EM Gain
- > 90% Quantum Efficiency
- Quantitative Performance
- New LightSpeed™ mode
- Includes full two year warranty
Evolve® 128 EMCCD Camera
Excellent for low-light imaging applications
The Evolve 128 delivers the highest frame rates available with extreme sensitivity for demanding low-light applications ranging from In Vivo imaging to Single Molecule Fluorescence. As the leader in quantitative performance, the Evolve 128 provides researchers an enhanced imaging tool with on board camera intelligence. Features such as Quant-View® combined with superior stability, enables precise and accurate research measurement and reproducible results.
- Measure and Quantify Your Data in Photoelectrons
- Streamline Workflow and Save Time
- Set the Standard in Your Research
- Includes full two year warranty
Evolve® 512 EMCCD Camera
Smallest, Most Powerful Scientific EMCCD Camera
The Evolve 512 "Intelligent" EMCCD camera is the first scientific imaging solution that reads out pixel data in photoelectrons, resulting in accurate and reproducible data. With the most advanced feature set available, this small, yet powerful Evolve camera is ideally suited for low-light bioimaging applications.
- Photo-Activated Localization Microscopy (PALM)
- Stochastic Optical Reconstruction Microscopy (STORM)
- Spinning disk confocal microscopy
- Total Internal Reflection Fluorescence (TIRF) microscopy
- Cell trafficking studies
- Live-cell fluorescent protein imaging
- Single Molecule Fluorescence (SMF)
Light Source - Monochromator
- High throughput F/2 corrected optic
- Integral fast electronic shutter on all models
The Optoscan monochromator from Cairn Research is the only instrument of its type to offer control of both centre-wavelength and bandwidth with millisecond time resolution. Combined with Cairn signal processing modules and optical hardware it forms the heart of a powerful and flexible microfluorescence system. Alternatively it can be readily integrated into commercial imaging systems, or custom controlled for bespoke applications.
This instrument has been designed specifically with real-time biological fluorescence measurements in mind, but has evolved into a truly versatile laboratory tool. If your application requires fast, flexible and automated illumination control then the Cairn Optoscan may well be the instrument of choice.
Other commercial monochromators include the facility to change bandwidth between experiments using a manual control. This is sufficient for many purposes, but is not ideal for complex protocols especially those involving multiple fluorescence markers. Only by controlling bandwidth in real-time during experiments can each excitation wavelength be optimised independently. This means that where Stoke’s shifts are large or where fluorescence intensities are weak then a relatively large bandwidth can be selected to maximise signal-to-noise. Conversely if there is a small Stoke’s shift or if the fluorescence intensity is high then the slit width can be minimised to reduce bleed through and optimise dynamic range.
MetaFluor Fluorescence Ratio Imaging Software
MetaFluor® Fluorescence Ratio Imaging Software is the industry standard for monitoring fluorescence ratio imaging applications, bringing microscopists closer to rapid cellular responses inherent to live cells.
MetaFluor Fluorescence Ratio Imaging Software is designed for dual-wavelength intracellular ion measurements. The system provides simultaneous display of the raw data; ratio image; graphs of intensities, ratios, and ion concentrations (e.g., calcium, sodium, potassium, chloride); and a non-ratiometric image such as a brightfield or phase-contrast image. Two different ratiometric indicators can be imaged and measured simultaneously to provide greater insight to ion exchange and intracellular function regardless of dye loading concentrations, conditions, or emission intensities.
Toolbars, menus, wizards, and dialog boxes help move you through the image processing steps quickly. Features such as multiple image windows, flexible device control, synchronization and timing, and journals allow for automated image acquisition and analysis unlike any other system.
With MetaFluor Fluorescence Software, you customize the set-up once, then let the experiment run by itself. You are able to collect a large amount of data online and process it with either MetaFluor Software or independently using an analysis-only software version.
MetaFluor Fluorescence Ratio Imaging Software features:
- Real time processing significantly reduces random image noise by averaging up to 256 images per time point. Background subtraction is also used to improve accuracy by correcting for stray light, camera noise, and auto-fluorescence.
- Calibrations of intracellular ion concentrations are obtained by using the various calibration options offered: the Grynkiewicz equation (Grynkiewicz et al., 1985) and titration equation for both in situ and in vitro experiments. These calibrations can then be stored for future use.
- Region analysis can be generated automatically or manually to monitor intensity, ratio value, or ion concentration. Measurements are then made simultaneously on all the regions of interest and update continuously on a scrolling graph, allowing you to follow dynamic changes as they occur in your living samples.
- Interactive graphs give flexibility in the presentation of your experiment's data. MetaFluor Software enables you to click on graph traces to display a readout of the time and data value for the region nearest to the click.
- Event mark function is useful to record when drugs or solutions are added, experimental conditions changed, triggers are received or sent, or other events occurred. You have the option to associate a timer and an alarm bell to each event. Additionally, for perfused samples, ambient conditions can be logged and tracked.
- Journals allow you to create functions to simplify system operations, automate acquisition and device control, set variables, and sequence events. The Auto-Execute Journal command allows you to automatically run journals at specific points in the acquisition cycle.
OASIS In Vivo Platform - Modular Macroscope and Microscope
Optical Activation, Stimulation & Imaging System
- Translates and Rotates for Live Animal Research
- Simultaneously Image & Deliver Wide-field and/or Pattern Illumination
- Macro or Microscopic Optical Assembly
- Modular Platform Tailors to any Experimental Application
- Excellent System for:
- In Vivo Optogenetics
Mightex's Optical Activation, Stimulation and Imaging System (OASIS) is designed specifically to meet the growing demand to conduct experiments on live animals, when system flexibility is a primary consideration and a large Field of View (FoV) is usually required. In Optogenetics, for example, in vivo patterned illumination on rodents, monkeys and other animals is the next step towards the ultimate goal of being able to record and control the activity of each neuron in the brain of behaving animals at a single cell and ms resolution. To achieve patterned illumination for in vivo applications, the OASIS features Mightex’s market-leading Polygon400 patterned Illuminator to deliver light to a specified area of the specimen while leaving neighboring areas untouched.
Whereas traditional microscopes are a fixed system with limited flexibility, OASIS is designed to provide excellent reconfigurability/flexibility and can be configured to work around a fixed specimen such as a sedated live animal. A heavy-duty precision XYZ stage is mounted on the support structure and the OASIS optical assembly is in turn mounted on the XYZ stage. The XYZ stage controls the lateral motion as well as focus of the system. A pan/tilt mechanism add-on is also available to orient the OASIS relative to the live animal. Motorized versions of both the XYZ stage and tilt mechanism are available.
OASIS Implant - Deep-Brain Imaging & Stimulation System for Freely Behaving Animals
- In vivo all-optical recording and manipulatiion of neural circuit activity;
- Sub-cellular resolution, high-quality imaging for quantitative analysis;
- Multi-wavelength illumination;
- Patterned stimulation with sub-cellular targeting capability;
- Super-light head mounted fixture, 0.3g;
- Modular system design, reconfigurable for different applications.
Mightex's OASIS Implant is a ground-breaking microendoscopic system that is capable of doing deep-brain simultaneous all-optical recording and manipulation of neural circuit activity with cellular resolution, on freely behaving animals. Compatible with high-sensitivity research-grade cameras, OASIS Implant enables researchers to acquire far superior quality deep-brain images & videos, compared to the relatively low-quality head-mounted cameras that have recently been introduced into the market. In addition, with multiple illumination ports, OASIS Implant is equipped with both wide-field and patterned illumination capabilities (when combined with Mightex's market-leading Polygon400) and, moreover, it is also capable of doing multi-wavelength imaging/stimulation which cannot be done with the existing head-mounted cameras. More importantly, since both the deep-brain imaging and the deep-brain stimulation are delivered through an Imaging Fiber bundle, the overall weight of the head-mounted fixture is as little as 0.3g (compared to approximately 2g with a head-mounted camera), making OASIS Implant an ideal research tool for in vivo live animal experiments.
In addition to many other applications, OASIS Implant enables bioscientists to do the following:
- Deep brain calcium imaging in freely behaving animals;
- Deep brain patterned optogenetic stimulation with single-cell or sub-cellular resolution;
- Simultaneous deep brain stimulation and imaging.
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