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Kính hiển vi huỳnh quang soi nổi Leica M205 FCA & Leica M205 FA

Model: M205 FCA & M205 FA
Tình trạng: Liên hệ
Leica Microsystems vừa phát triển dòng kính hiển vi huỳnh quang soi nổi mới M205 FA và M205 FCA hỗ trợ nghiên cứu biểu hiện biến đổi gen như GFP và mCherry trong giai đoạn sớm, cho phép bạn lựa chọn mẫu phù hợp để đạt kết quả trong nghiên cứu.
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Do you sometimes feel like you are fishing in the dark because you are looking for fluorescence signals that are increasingly faint and weak? Brightness and high resolution images are a must in modern developmental biology and research.

Leica Microsystems has developed the M205 FA and M205 FCA fluorescence stereo microscopes to enable you to detect transgenic expression like GFP and mCherry in early stages, allowing you to select the right sample to successfully base your studies on.

 

Leica M205 FCA: semi-automated with manual zoom

 

Until now, you probably had to switch between two different systems: one for fast screening with a manual zoom that is intuitive to maneuver and a high-end solution to see and capture the faintest signals in an image.

 

The Leica M205 FCA fluorescence stereo microscope unites both worlds and combines super-fast manual screening with high-end imaging capabilities.

 

 
 
Video of c.elegans pharynx with mCherry. Courtesy of Martin Gamerdinger, Ph.D., Scientific Project Leader, Molecular Microbiiology, University o Constance, Germany

 

Now you can have it all:

  • Get highly reliable and publishable results as all parameters are always auto-stored for you
  • Eliminate interruption in your workflow with the four position coded filter changer
  • Add a footswitch for easy change of filters, focus, and illumination adjustment, keeping both hands free for screening

 

Discover the automated world of research

 

Leica M205 FA fully motorized fluorescence stereo microscope

 

The Leica M205 FA opens up a new world of research in fluorescence microscopy, for instance when working in a sterile cabinet.

  • Easily handle complex multi-channel fluorescence imaging procedures
  • Execute demanding experiments with the motorized zoom, filter changer, Fluroescence Intensity Manager (FIM), and iris diaphragm
  • Get high resolution at the stage level: the Leica LMT 260 scanning stage positions your sample in the sub-um range and holds life cell incubation equipment

 

 

Bright fluorescence signals – always.

 

To detect even the faintest signals of your sample, you need an energy-rich excitation light to give a bright fluorochrome signal.

However, the excitation light may cause reflections that blur the black background and compromise the detection of fluorescence signals.

Leica’s TripleBeam technology completely eliminates this background “noise” by introducing a third optical zoom. This separates the fluorescence excitation light from the two observation channels and omits the need for a dichroic mirror.

The result is a clear and strong fluorescence signal against a noise-free, black background.

 
 
 
 
 
 

Finest details in 3D

 

Do you think that high resolution and maximum depth of field are irreconcilable opposites in microscopy? We prove they are not! Leica Microsystems' FusionOptics technology overcomes optical limitations by using the two beam paths for different tasks:

  • The right channel delivers a high-resolution image at the largest possible numerical aperture.
  • The left channel presents an image with high depth of field.

The result: you perceive an image with outstanding richness of detail and exceptional depth of field at the same time

 

Microscopic resolution in a stereo

 

Recognizing fine details is vital in research especially when working with small organisms. The Leica M205 FA and M205 FCA can achieve a resolution of 1279 lp/mm or 0.78 µm based on the resolution limit defined in ISO18221*.

The 2.0x PlanApo objective is an optical masterpiece. It has a maximum aperture of 0.35 – that’s the highest numerical aperture (NA) that has ever been achieved with a stereo microscope. This is smaller than a tenth of the diameter of a human red blood cell.

*M205 FA, 2x PlanAPO objective, camera adapter 0.63x, DMC4500 camera in full frame mode, Apple 5K with 27” monitor.

 

 
 
Neuronal cell culture stained with DAPI, beta III Tubulin–Cy2, Nestin-Cy3 (LMS Bioanalytik GmbH, Magdeburg, Germany). Blue indicates the nuclei of the cells, green neurons expressing beta III Tubulin, and red stem cells expressing Nestin. Image was acquired with a M205 FCA stereo microscope, LMT260 x/y stage, DFC3000 G microscope camera and Fluocombi III at 400x.
 
 
 
Zebrafish, mpx:eGFP line: time lapse images of the neutrophils to the tail resection. Courtesy of Dr Carl Tucker, The Queen’s Medical Research Institute, University Edinburgh, United Kingdom. In this in vivo model the inflammatory response in a transgenic zebrafish line that expresses GFP under the neutrophil-specific myeloperoxidase promoter is shown. “Quantitative data can be generated from this model by counting of fluorescent cells or by digital image analysis” (Renshaw et al Blood 2006) DOI 10.1182/blood-2006-05-024075
 
 

Speed matters – encoding helps

 

Image Coding provides convenient, reproducible settings for quick, easy documentation.

The integrated encoding transmits both the magnification and the position of the iris diaphragm to the software in real time. A scale bar is overlayed into the live image and updated when the magnification is changed. When an image is stored, all the settings are saved with the image and can be recalled at any time.

  • Coded components offer ease of use and reliable results even for untrained operators
  • The microscope system is intelligently linked to the software to allow you to change settings without having to manually adjust the calibration
  • TL5000 Ergo transmitted light base adapts the aperture automatically to the zoom position to deliver optimal contrast

 

2 x CORR objective – making it clear!

 

With the Leica PLAN APO 2.0x CORR Objective, the refractive index can be adjusted – this way you will have pin-sharp images even if there is a water column of 5 mm between your sample and the objective. The objective enables users to observe and document samples as if the water did not exist.

When observing samples immersed in a watery solution, structures tend to blur especially in high magnification. This is due to the refractive index mismatch of air (index = 1) and water (index = 1.3). Potentially interesting or important structures may be easily misinterpreted because of spherical aberrations that may occur, as regular objectives are dedicated to the use with samples surrounded by air only.

 
 
Fluorescence video imaging of a zebrafish larva expressing green fluorescent protein (GFP) immersed in an aqueous solution. The images were captured with a Leica M165 FC stereo microscope where a Leica 2x Plan Apo objective with (right image) and without (left image) correction collar was used. The heart of the zebrafish larva is seen beating in both videos. The larva appears blurrier in the non-corrected image on the right. Courtesy of M. J. Hamm and W. Herzog, Angiogenesis Laboratory, Max Planck Institute for Molecular Biomedicine and Westfälische Wilhelms University in Münster, Germany.
 
 
 
 
Solea senegalensis larvae nervous system, max projection of a tile scan of 6 fields x 33 planes. Parallax correction and tiling performed in LAS X after deconvolution with Huygens professional. Courtesy of Dr. Marco A. Campinho, CCMAR - Centre for Marine Sciences, Universidade do Algarve, Portugal.
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Work More Efficiently in Developmental Biology With Stereo Microscopy: Zebrafish, Medaka, and Xenopus

 

 

Work More Efficiently in Developmental Biology With Stereo Microscopy: Zebrafish, Medaka, and Xenopus

 

Among the aquatic model organisms used in molecular and developmental biology the most prominent are the zebrafish (genus species: Danio rerio), medaka or japanese rice fish (genus species: Oryzias latipes), and african clawed frog (genus species: Xenopus laevis). This report gives useful information to scientists and technicians which can help improve their daily laboratory work by making the steps of transgenesis, fluorescent screening, and functional imaging more efficient.

 

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For samples/specimens immersed in a liquid or embedded in a polymer, high quality microscopic observation can be hindered as a result of spherical aberration. An objective which can correct for refractive index mismatch allows images with greatly reduced spherical aberration and sharper focus to be obtained.

 

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Work Efficiently in Developmental Biology with Stereo and Confocal Microscopy: C. elegans

 

For scientists, technicians, and teachers working with the worm C. elegans in the research lab or classroom, this report is intended to give useful information to help improve their daly work. The aim is to make the work steps of worm picking, transgenesis, RNA interference, screening, and functional imaging efficient. It also details the various possibilities for equipping a research worm lab or biology classroom/teaching lab explaining worm methods.

 

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For scientists and technicians working with fruit flies, most often genus Drosophila, this report is intended to give useful information to help improve daily laboratory work by making the steps of fly pushing, fluorescent screening, dissection, and documentation/imaging more efficient. It also details various possibilities for properly equipping or stocking a fly lab.