ZEISS Microscopy Course Catalog
|
|
|
- Janel Oliver
- 10 years ago
- Views:
Transcription
1 ZEISS Microscopy Course Catalog
2
3 ZEISS Training and Education Expand Your Possibilities Practical microscopy training has a long tradition at ZEISS. The first courses were held in Jena as early as 1907, initiated by two notable ZEISS scientists, Henry Siedentopf and August Koehler. The courses have since been continuously advanced and updated. Our own continuous education as well as cooperation projects with scientists in high-ranking laboratories ensure that we are always up to date. Our courses impart the theoretical background as well as practical skills in many applications from biology, medicine and materials science. Lectures are immediately followed by practical hands-on trainings in small groups. And you will get comprehensive course material, which you can refer to when practicing your newly acquired skills and knowledge at your place. Our trainers are graduated scientists and bring together knowledge in various scientific fields with several years of experience in microscopy and its practical application. This combination of technical and applications know-how is just the right mixture to get your theoretical and practical questions answered. At our applications centers you have access to various combinations of microscopes of the latest generation of our systems from the simple course microscope to digital imaging systems. Our courses offer maximum efficiency during theoretical and practical learning with the most modern systems. There is no better access to learn the diversity of microscopical applications. We also offer customized courses at your facility to meet your special requirements. If you need professional support for your courses, we would like to help with our expertise. ZEISS Microscopy Training Team Please visit for further information, our current schedule and the registration form.
4 Course Directory Interactive content: Please click on the course you would like to go. Laser Scanning Microscopy Courses Fluorescence Correlation Spectroscopy (FCS) in Biomedical Research Lightsheet Z.1: Principle, Sample Preparation and Applications LSM 7 Generation for Biomedical Applications - Part LSM 7 Generation for Biomedical Applications - Part LSM Biomedical Applications LSM 880 for Biomedical Applications - Part LSM 880 for Biomedical Applications - Part Multiphoton Laser Scanning Microscopy RICS: Raster Image Correlation Spectroscopy Specifically Arranged Trainings - Laser Scanning Microscopy Superresolution Microscopy: PALM, dstorm and Structured Illumination Light Microscopy Courses Grains Analysis Graphite Analysis Image Analysis for everyone Image Analysis with AxioVision Non-Metallic-Inclusions (NMI) Particle Analyzer Specifically Arranged Trainings - Light Microscopy Courses OAD Macro-Programming for ZEN
5 Laser Scanning Microscopy Courses A picture created from a confocal (LSM 710) image of developing eggs from the ovary of the parasitic wasp Microplitis demolitor. Biomedical Microscopy Core, University of Georgia, Athens, GA
6 Fluorescence Correlation Spectroscopy (FCS) in Biomedical Research Advanced Users Fluorescence Correlation Spectroscopy (FCS) is a highly sensitive method that detects movement and binding of fluorescence-labelled particles on the single molecule level. Furthermore concentrations of movable fluorescent particles can be estimated. Thus biochemical reactions can be monitored in real time solutions as well as within living cells. This course will familiarize you with the theoretical background of FCS and train you on how to perform and evaluate measurements in solutions and living cells. Topics Theory of FCS Correlation function Model functions for diffusion processes Data acquisition for FCS Data analysis for FCS Objective lenses for FCS and FCCS Numbers and brightness Systems FCS capable systems (LSM 880, LSM BiG.2) ZEN (black edition) Prerequisites Topics can be adapted to specific needs, depending on the particular prior knowledge. Application Center Jena 2 day(s) Participants min. 3, max. 4 SAP No
7 Lightsheet Z.1: Principle, Sample Preparation and Applications Beginners and Advanced Users Light sheet microscopy by ZEISS is a completely novel technique in biomedical research, dedicated for live cell imaging. Excellent knowledge of its theory and application is a prerequisite for experimental success. After this course you will understand the theory on light sheet microscopy, how to prepare a sample for light sheet imaging, acquisition of a light sheet sample, and how to process the acquired images. Topics The beam path Sample preparation and chamber building Single Side Illumination and Dual Side Illumination Pivot scanning Multiview Quick Setup and Manual Setup Incubation Dual Side Fusion and subsetting Multiview Processing: landmark, intensity, and interactive registration with Fusion Online processing Deconvolution Customer interfaces and system care Systems Lightsheet Z.1 Prerequisites Basic knowledge in light and fluorescence microscopy Application Center Jena 5 day(s) Participants min. 2, max. 3 SAP No
8 LSM 7 Generation for Biomedical Applications Part 1 Beginners Laser Scanning Microscopy is a standard method in biomedical research. Excellent knowledge of its theory and application is a prerequisite for experimental success. In this course you will master the skills required for professional operation of our laser scanning microscopes including high-quality imaging of three dimensional samples, of multi fluorophore labeled samples and basic quantitative image analysis. Topics Principle and beam paths of confocal laser scanning microscopy Image acquisition and optimization Multiple fluorophore imaging and channel-based linear unmixing 3D image acquisition and reconstruction Basic image analysis and colocalization System care and maintenance (SMT Tool, ConfigTool, etc) Selecting objective lenses for laser scanning microscopy Systems LSM 7 Generation (710, 780,700) ZEN (black edition) Prerequisites Basic knowledge in light and fluorescence microscopy Only at customer site 2 day(s) Participants min. 4, max. 6 SAP No
9 LSM 7 Generation for Biomedical Applications Part 2 Advanced Users Besides their classical function as superior 2D and 3D imaging systems, advanced laser scanning microscopes can be applied to study subcellular dynamics and to separate multiple fluorescent labels in a live cell environment. Confocal microscopy of living cells requires to optimize imaging for speed and minimal light induced lesions. If fluorescent labels with overlapping emission spectra are combined, simultaneous spectral acquisition followed by linear umixing can be used to separate them from each other. Different photo manipulation techniques provide information about dynamic properties of the labelled components. Learn to master these innovative experimental approaches during this course to apply them successfully in your own research. Topics Strategies for multiple fluorophore imaging Lambda stack acquisition, linear unmixing, and online fingerprinting Live cell imaging strategies Photomanipulation of dyes (photoconversion and photoactivation) FRAP (Fluorescence Recovery After Photobleaching) FRET (Forster Resonance Energy Transfer) Tiles and positions, ROI High Dynamic Range Imaging, 3D VisArt Systems LSM 7 Generation (710, 780,700) ZEN (black edition) Prerequisites LSM 7 Generation in Biomedical Applications - Part 1 or equivalent knowledge Only at customer site 3 day(s) Participants min. 4, max. 6 SAP No
10 LSM Biomedical Applications Beginners Laser Scanning Microscopy is a standard method in biomedical research. Excellent knowledge of its theory and application is a prerequisite for experimental success. This course provides detailed knowledge about point scanning confocal microscopes in respect to its assembly, features and application in biomedical sciences. Topics Theory of laser scanning confocal microscopy Beam paths and configurations of the LSM 700 Variable Secondary Dichroic Beamsplitter (VSD) and how to use it Emission filters and Cross-talk avoidance Image acquisition and optimization Multiple fluorophore imaging and channel-based linear unmixing Lambda Stack acquisition and linear unmixing Basic image analysis and colocalization 3D image acquisition and reconstruction System maintenance and care (SMT, ConfigTool, etc) Selecting objective lenses for laser scanning microscopy Systems LSM 7 Generation Prerequisites Basic knowledge in light microscopy Only at customer site 3 day(s) Participants min.3, max. 4 SAP No
11 LSM 880 for Biomedical Applications - Part 1 Beginners Laser Scanning Microscopy is a standard method in biomedical research. Excellent knowledge of its theory and application is a prerequisite for experimental success. In this course you will master the skills required for professional operation of our laser scanning microscopes including high-quality imaging of three dimensional samples, of multi fluorophore labeled samples and basic quantitative image analysis. Topics Principle and beam paths of confocal laser scanning microscopy Image acquisition and optimization Multiple fluorophore imaging and channel-based linear unmixing 3D image acquisition and reconstruction Basic image analysis and colocalization System care and maintenance (SMT Tool, ConfigTool, etc) Selecting objective lenses for laser scanning microscopy Systems LSM 880 ZEN (black edition) Prerequisites Basic knowledge in light and fluorescence microscopy Application Center Jena 2 day(s) Participants min. 4, max. 6 SAP No
12 LSM 880 for Biomedical Applications - Part 2 Advanced Users Besides their classical function as superior 2D and 3D imaging systems, advanced laser scanning microscopes can be applied to study subcellular dynamics and to separate multiple fluorescent labels in a live cell environment. Confocal microscopy of living cells requires to optimize imaging for speed, minimal light induced lesions and highest achievable resolution. If fluorescent labels with overlapping emission spectra are combined, simultaneous spectral acquisition followed by linear umixing can be used to separate them from each other. Different photo manipulation techniques provide information about dynamic properties of the labelled components. Learn to master these innovative experimental approaches during this course to apply them successfully in your own research. Topics Strategies for multiple fluorophore imaging Lambda stack acquisition, linear unmixing, and online fingerprinting Live cell imaging strategies Photomanipulation of dyes (photoconversion and photoactivation) FRAP (Fluorescence Recovery After Photobleaching) FRET (Forster Resonance Energy Transfer) Airyscan (confocal, virtual pinhole and superresolution imaging) Systems LSM 880 with Airyscan ZEN (black edition) Prerequisites LSM 880 in Biomedical Applications - Part 1 or equivalent knowledge Application Center Jena 3 day(s) Participants min. 4, max. 6 SAP No
13 Multiphoton Laser Scanning Microscopy Beginners and Advanced Users Multiphoton microscopy enables due to the far red excitation deep tissue imaging and is thereby gentle on your sample. After this course, you will understand the theory of non-linear optical microscopy, the beam path, how to use the system, how to perform excitation fingerprinting, second harmonic generation, and Non-Descanned Detection. Topics Theory of Multiphoton laser scanning microscopy Beam paths and configurations of NLO systems Objective lenses for Multiphoton Dodt contrast Non-Descanned Detection and NDD filter sets Excitation fingerprinting Second harmonic generation System maintenance and care Systems LSM 880 NLO Prerequisites LSM 880 for Biomedical Applications - Part 2 or LSM 7 Generationfor Biomedical Applications - Part 2 or equivalent knowledge Application Center Jena 2 day(s) Participants min. 2, max. 3 SAP No
14 RICS: Raster Image Correlation Spectroscopy Advanced Users We will provide the skills to acquire images from living cells for RICS and enable you to analyze RICS images based on simple fitting models. Topics Theory of RICS The correlation image Image acquisition for RICS Fitting models for diffusion processes Data analysis for RICS Diffusion and correlation maps Systems LSM 880 Prerequisites LSM 880 for Biomedical Applications - Part 2 or LSM 7 Generation for Biomedical Applications - Part 2 Fluorescence Correlation Spectroscopy (FCS) in Biomedical Research or equivalent knowledge Application Center Jena 1 day(s) Participants min. 3, max. 4 SAP No
15 Specifically Arranged Trainings - Laser Scanning Microscopy Beginners and Advanced Users If you have a special training request of microscopy topics not covered in this catalog, please feel free to contact us. Topics Tailored according to request Systems Selection of current ZEISS systems ZEISS Microscopy software Prerequisites None Application Center Jena 1-5 day(s) Participants n.a. SAP No
16 Superresolution Microscopy: PALM, dstorm and Structured Illumination Advanced Users Superresolution microscopy is a novel technique that enables insights into structures beyond the classical resolution limit. In essence there are two major superresolution techniques available. One is based on a structured illumination approach (SIM), the other depends on activatable or photo-switchable fluorophores. This course will provide the skills to acquire SR-SIM, PALM, and dstorm data from specimens and will enable you to perform the appropriate processing. Topics Localization microscopy basics and applications Comparison: PALM vs. dstorm PALM: multichannel imaging PALM: grouping and working with fiducials PALM: activation strategies PALM: 3D PALM SR-SIM SR-SIM: basics, acquisition, and filtering SR-SIM: channel alignment SR-SIM: sample preparation PSF Processing Systems Elyra system Prerequisites Basic knowledge in widefield and fluorescence microscopy LSM 880 for Biomedical Applications - Part 1 and Part 2 or LSM 7 Generation for Biomedical Applications - Part 1 and Part 2 Application Center Jena 4 day(s) Participants min. 2, max. 3 SAP No
17 Light Microscopy Courses Duodenum Frog. Azan-Staining. Plan-APOCHROMAT 63/ 1.40 Oil, Michael Zölffel, ZEISS Microscopy
18 Grains Analysis Beginners and Advanced Users Deepen the knowledge about grains analysis using AxioVision Grains software with your samples. Topics Presentation of applications, hardware, accessories, resolution, segmentation, ISO and workflow AxioVision Grains software demo Reporting and archives Real measurements on customer s samples AxioVision Grains analysis Prerequisites None Remote Training 4 hour(s) Participants max. 8 SAP No
19 Graphite Analysis Beginners and Advanced Users Deepen the knowledge about graphite analysis using AxioVision Graphite software with your samples. Topics Presentation of applications, hardware, accessories, resolution, segmentation, ISO and workflow AxioVision Graphite software demo Reporting and archives Real measurements on customer s samples AxioVision Graphite analysis Prerequisites None Remote Training 4 hour(s) Participants max. 8 SAP No
20 Image Analysis for everyone Beginners Solving image analysis problems with the AxioVision modules Imaging Plus, AutoMeasure Plus, Commander, or with ZEN 2 (blue edition) / ZEN 2 core modules Advanced Processing & Analysis and OAD-macro editor. Topics introduction to image analysis Image processing functions Image segmentation functions The specific functions of AxioVision/ZEN Scripting using the AxioVision module Commander, and the macro editor in ZEN 2 (blue edition) / ZEN 2 core AxioVision ZEN 2 (blue edition) ZEN 2 core Prerequisites knowledge in digital photography Application Center Göttingen 5 day(s) Participants 6 SAP No
21 Image Analysis with AxioVision Beginners Deepen the knowledge about image analysis using AxioVision. Topics Presentation of applications, resolution, segmentation, workflow, software tools and scripts with Commander AxioVision software demo AxioVision Prerequisites None Remote Training 3 hour(s) Participants max. 8 SAP No
22 Non-Metallic-Inclusions (NMI) Beginners and Advanced Users Deepen the knowledge about non-metallic-inclusions (NMI) using AxioVision NMI software with your samples. Topics Presentation of applications, hardware, accessories, resolution, segmentation, ISO and workflow AxioVision NMI software demo Reporting and archives Real measurements on customer s samples AxioVision NMI Prerequisites None Remote Training 6 hour(s) Participants max. 8 SAP No
23 Particle Analyzer Beginners and Advanced Users Deepen the knowledge about Particle Analyzer using AxioVision Particle Analyzer software with your samples. Topics Presentation of applications, hardware, accessories, resolution, segmentation, ISO and workflow AxioVision Particle Analyzer software demo Scripts with Commander Reporting and archives Real measurements on customer s samples AxioVision Particle Analyzer Prerequisites None Remote Training 6 hour(s) Participants max. 8 SAP No
24 Specifically Arranged Trainings - Light Microscopy Beginners and Advanced Users If you have a special training request of microscopy topics not covered in this catalog, please feel free to contact us. Topics Tailored according to request Systems Selection of current ZEISS systems ZEISS Microscopy software Prerequisites None Application Center Göttingen 1-5 day(s) Participants n.a. SAP No
25 Courses LSM 880, ZEN, Experiment Designer, ZEISS Microscopy
26 OAD Macro-Programming for ZEN Beginners and Advanced Users This course provides the skills to generate automatic routines with Python, ZEN and image processing. The participants are acquainted with the basics of the ZEN object model. The most important ZEN objects (camera, microscope, image, annotations, image processing, measurement, dialogs) are illustrated. The comprehension of the ZEN object model is improved by means of practical exercises. Topics Introduction of IronPython programming environment of ZEN Basics and utilities for Python programming Overview of the ZEN object model Explanations of the ZEN objects with hands-on exercises Practical applications (generation of ZEN macros) ZEN 2012 (blue edition) Prerequisites Good knowledge in an object-oriented programming language and ZEN software Valid licence of ZEN (MacroEnvironment, analysis, advanced processing) Microscopy Labs Munich 2 day(s) Participants 6 SAP No
27
28 CZ-10/2013 Content, design and technical information is subject to change. Carl Zeiss Microscopy GmbH Carl Zeiss Microscopy GmbH Jena, Germany Last update: August 2015
29 Price List ZEISS Site Customer Site Course Course Fee per person SAP No. Course Fee per course SAP No. Laser Scanning Microscopy Courses Fluorescence Correlation Spectroscopy (FCS) in Biomedical Research Lightsheet Z.1: Principle, Sample Preparation and Applications LSM 7 Generation for Biomedical Applications - Part 1 LSM 7 Generation for Biomedical Applications - Part , , , , n/a n/a 2.660, n/a n/a 5.250, LSM Biomedical Applications n/a n/a 3.990, LSM 880 for Biomedical Applications - Part , , LSM 880 for Biomedical Applications - Part , , Multiphoton Laser Scanning Microscopy 1.750, , RICS: Raster Image Correlation Spectroscopy 1.050, , Specifically Arranged Trainings - Laser Scanning Microscopy 1.050,00 (costs per day) ,00 (costs per day) Superresolution Microscopy: PALM, dstorm and Structured Illumination 3.500, , Light Microscopy Courses Grains Analysis 400, n/a n/a Graphite Analysis 400, n/a n/a Image Analysis for everyone 3.500, , Image Analysis with AxioVision 300, n/a n/a Non-Metallic-Inclusions (NMI) 600, n/a n/a Particle Analyzer 600, n/a n/a Specifically Arranged Trainings - Light Microscopy 1.050,00 (costs per day) ,00 (costs per day) Courses OAD Macro-Programming for ZEN All prices are net prices and subject to VAT statutory rate. Valid from February 1 st, All information are subject to change.
Zeiss 780 Training Notes
Zeiss 780 Training Notes 780 Start Up Sequence Do you need the argon laser, 458,488,514nm lines? No Turn on the Systems PC Switch Turn on Main Power Switch Yes Turn on the laser main power switch and turn
Usage guidelines for the Advanced Light Microscopy Technology Platform (ALM) at the Max-Delbrück-Center, Berlin
Usage guidelines for the Advanced Light Microscopy Technology Platform (ALM) at the Max-Delbrück-Center, Berlin The following guidelines apply to all internal and external user of the ALM. The purpose
Information about ZEN 2009 Service Pack 2
Information about ZEN 2009 Service Pack 2 Build 5.5.0.443, SMT 5.5.3.1 The Service Pack 2 is a full installation for ZEN 2009 and ZEN 2009 SP1. It is required that ZEN 2009 is available on the system before
Principles of Microscopy and Confocal and Fluorescence Microscopy
Principles of Microscopy and Confocal and Fluorescence Microscopy Content This course in Light Microscopy follows the series of successful courses in Light Microscopy, Confocal and Fluorescence Microscopy
Lecture 20: Scanning Confocal Microscopy (SCM) Rationale for SCM. Principles and major components of SCM. Advantages and major applications of SCM.
Lecture 20: Scanning Confocal Microscopy (SCM) Rationale for SCM. Principles and major components of SCM. Advantages and major applications of SCM. Some limitations (disadvantages) of NSOM A trade-off
Zeiss Axioimager M2 microscope for stereoscopic analysis.
Zeiss Axioimager M2 microscope for stereoscopic analysis. This system is fully motorized and configured with bright field and multi-channel fluorescent. It works with Stereo Investigator, Neurolucida,
Microscopy: Principles and Advances
Microscopy: Principles and Advances Chandrashekhar V. Kulkarni University of Central Lancashire, Preston, United kingdom May, 2014 University of Ljubljana Academic Background 2005-2008: PhD-Chemical Biology
AxioCam HR The Camera that Challenges your Microscope
Microscopy from Carl Zeiss AxioCam HR The Camera that Challenges your Microscope Documentation at the edge of the visible The Camera for Maximum Success: AxioCam HR Low light fluorescence, live cell imaging,
Confocal Microscopy and Atomic Force Microscopy (AFM) A very brief primer...
Confocal Microscopy and Atomic Force Microscopy (AFM) of biofilms A very brief primer... Fundamentals of Confocal Microscopy Based on a conventional fluorescence microscope Fluorescent Microscope Confocal
Thermo Scientific ArrayScan XTI High Content Analysis Reader. revolutionizing cell biology with the power of high content
Thermo Scientific ArrayScan XTI High Content Analysis Reader revolutionizing cell biology with the power of high content learn more about your cells using high content technology Thermo Scientific High
Euro-BioImaging European Research Infrastructure for Imaging Technologies in Biological and Biomedical Sciences
Euro-BioImaging European Research Infrastructure for Imaging Technologies in Biological and Biomedical Sciences WP11 Data Storage and Analysis Task 11.1 Coordination Deliverable 11.3 Selected Standards
AxioCam MR The All-round Camera for Biology, Medicine and Materials Analysis Digital Documentation in Microscopy
Microscopy from Carl Zeiss AxioCam MR The All-round Camera for Biology, Medicine and Materials Analysis Digital Documentation in Microscopy New Dimensions in Performance AxioCam MR from Carl Zeiss Both
pco.edge 4.2 LT 0.8 electrons 2048 x 2048 pixel 40 fps 37 500:1 > 70 % pco. low noise high resolution high speed high dynamic range
edge 4.2 LT scientific CMOS camera high resolution 2048 x 2048 pixel low noise 0.8 electrons USB 3.0 small form factor high dynamic range 37 500:1 high speed 40 fps high quantum efficiency > 70 % edge
Fluorescence Microscopy for an NMR- Biosensor Project
Fluorescence Microscopy for an NMR- Biosensor Project Ole Hirsch Physikalisch-Technische Bundesanstalt Medical Optics Abbestr. -1, 10587 Berlin, Germany Overview NMR Sensor Project Dimensions in biological
Fluorescent dyes for use with the
Detection of Multiple Reporter Dyes in Real-time, On-line PCR Analysis with the LightCycler System Gregor Sagner, Cornelia Goldstein, and Rob van Miltenburg Roche Molecular Biochemicals, Penzberg, Germany
Optical mesoscopy with a new giant lens. Gail McConnell, Johanna Tragardh, John Dempster & Brad Amos
Optical mesoscopy with a new giant lens Gail McConnell, Johanna Tragardh, John Dempster & Brad Amos The spot on specimen, source and detector aperture are at conjugate optical foci detector Advantage:
How To Use An Edge 3.1 Scientific Cmmos Camera
edge 3.1 scientific CMOS camera high resolution 2048 x 1536 pixel low noise 1.1 electrons global shutter USB 3.0 small form factor high dynamic range 27 000:1 high speed 50 fps high quantum efficiency
Technical Note. Roche Applied Science. No. LC 19/2004. Color Compensation
Roche Applied Science Technical Note No. LC 19/2004 Purpose of this Note Color The LightCycler System is able to simultaneously detect and analyze more than one color in each capillary. Due to overlap
Recording the Instrument Response Function of a Multiphoton FLIM System
Recording the Instrument Response Function of a Multiphoton FLIM System Abstract. FLIM data analysis in presence of SHG signals or extremely fast decay components requires the correct instrument response
MetaMorph Software Basic Analysis Guide The use of measurements and journals
MetaMorph Software Basic Analysis Guide The use of measurements and journals Version 1.0.2 1 Section I: How Measure Functions Operate... 3 1. Selected images... 3 2. Thresholding... 3 3. Regions of interest...
IMAGING SOFTWARE Advanced Image Deconvolution Capture, and Process, Visualization Measure, Software and Share For complete product information, please visit: www.mediacy.com/autoquant ADVANCED DECONVOLUTION
The How Do Guide to AxioVision. Author: Brian Svedberg Image Analysis Specialist Carl Zeiss MicroImaging, Inc.
The How Do Guide to AxioVision Author: Brian Svedberg Image Analysis Specialist Carl Zeiss MicroImaging, Inc. How do I grab a single image? How do I grab a single image? Click on the Camera icon to switch
FRET Basics and Applications an EAMNET teaching module
FRET Basics and Applications an EAMNET teaching module Timo Zimmermann + Stefan Terjung Advanced Light Microscopy Facility European Molecular Biology Laboratory, Heidelberg http://www.embl.de/almf/ http://www.embl.de/eamnet/
Invitation Workshop «Get the most out of your sample» - The perfect workflow for your sample
Invitation Workshop «Get the most out of your sample» - The perfect workflow for your sample University of Bern, Institute of Anatomy, Bern April 20 th -21 st, 2016 Sample: courtesy of S. Traikov, BIOTEC,
ParaVision 6. Innovation with Integrity. The Next Generation of MR Acquisition and Processing for Preclinical and Material Research.
ParaVision 6 The Next Generation of MR Acquisition and Processing for Preclinical and Material Research Innovation with Integrity Preclinical MRI A new standard in Preclinical Imaging ParaVision sets a
Fast Z-stacking 3D Microscopy Extended Depth of Field Autofocus Z Depth Measurement 3D Surface Analysis
Cam CANIMPEX CPX-SOLUTIONS 3D Digital Microscope Camera FAST PRECISE AFFORDABLE 3D CAMERA FOR MICROSCOPY Fast Z-stacking 3D Microscopy Extended Depth of Field Autofocus Z Depth Measurement 3D Surface Analysis
CONFOCAL LASER SCANNING MICROSCOPY TUTORIAL
CONFOCAL LASER SCANNING MICROSCOPY TUTORIAL Robert Bagnell 2006 This tutorial covers the following CLSM topics: 1) What is the optical principal behind CLSM? 2) What is the spatial resolution in X, Y,
Molecular Spectroscopy
Molecular Spectroscopy UV-Vis Spectroscopy Absorption Characteristics of Some Common Chromophores UV-Vis Spectroscopy Absorption Characteristics of Aromatic Compounds UV-Vis Spectroscopy Effect of extended
Applications of confocal fluorescence microscopy in biological sciences
Applications of confocal fluorescence microscopy in biological sciences B R Boruah Department of Physics IIT Guwahati Email: [email protected] Page 1 Contents Introduction Optical resolution Optical
A VERYbrief history of the confocal microscope 1950s
Confocal Microscopy Confocal Microscopy Why do we use confocal microscopy? A brief history of the confocal microscope Advantages/disadvantages of a confocal microscope Types of confocal microscopes The
Measuring the Point Spread Function of a Fluorescence Microscope
Frederick National Laboratory Measuring the Point Spread Function of a Fluorescence Microscope Stephen J Lockett, PhD Principal Scientist, Optical Microscopy and Analysis Laboratory Frederick National
Two-photon FCS Tutorial. Berland Lab Department of Physics Emory University
Two-photon FCS Tutorial Berland Lab Department of Physics Emory University What is FCS? FCS : Fluorescence Correlation Spectroscopy FCS is a technique for acquiring dynamical information from spontaneous
Neuro imaging: looking with lasers in the brain
Neuro imaging: looking with lasers in the brain Aim: To image life cells, label free, with cellular resolution in deep tissue Marloes Groot Vrije Universiteit Amsterdam Faculteit Exacte Wetenschappen Natuurkunde
Fundamentals of Image Analysis and Visualization (the short version) Rebecca Williams, Director, BRC-Imaging
Fundamentals of Image Analysis and Visualization (the short version) Rebecca Williams, Director, BRC-Imaging A digital image is a matrix of numbers (in this case bytes) 6 2 4 4 2 0 2 0 2 4 4 4 4 8 12 4
NyONE - Cell imaging in a bird s eye view 4. NyONE...resolution matters! 8. Features & benefits 10. Fluorescence excitation channels 12
Envisions confirmed Content NyONE - Cell imaging in a bird s eye view 4 From cells to numbers 6 NyONE...resolution matters! 8 Features & benefits 10 Fluorescence excitation channels 12 Technical specifications
Application of Automated Data Collection to Surface-Enhanced Raman Scattering (SERS)
Application Note: 52020 Application of Automated Data Collection to Surface-Enhanced Raman Scattering (SERS) Timothy O. Deschaines, Ph.D., Thermo Fisher Scientific, Madison, WI, USA Key Words Array Automation
Subject Area(s) Biology. Associated Unit Engineering Nature: DNA Visualization and Manipulation. Associated Lesson Imaging the DNA Structure
Subject Area(s) Biology Associated Unit Engineering Nature: DNA Visualization and Manipulation Associated Lesson Imaging the DNA Structure Activity Title Inside the DNA Header Image 1 ADA Description:
product overview pco.edge family the most versatile scmos camera portfolio on the market pioneer in scmos image sensor technology
product overview family the most versatile scmos camera portfolio on the market pioneer in scmos image sensor technology scmos knowledge base scmos General Information PCO scmos cameras are a breakthrough
ZEISS Axiocam 506 color Your Microscope Camera for Imaging of Large Sample Areas Fast, in True Color, and High Resolution
Product Information Version 1.0 ZEISS Axiocam 506 color Your Microscope Camera for Imaging of Large Sample Areas Fast, in True Color, and High Resolution ZEISS Axiocam 506 color Sensor Model Sensor Pixel
Webex-based remote instrument control guide
Webex-based remote instrument control guide 1) Once a microscopic imaging experiment is scheduled, the host (i.e., Hunter Bioimaging Facility) will send an email containing a Webex meeting link to the
Software Guide. ZEN 2 (blue edition)
Software Guide ZEN 2 (blue edition) Carl Zeiss Microscopy GmbH Carl-Zeiss-Promenade 10 07745 Jena, Germany [email protected] www.zeiss.com/microscopy Carl Zeiss Microscopy GmbH Königsallee 9-21 37081
DMBI: Data Management for Bio-Imaging.
DMBI: Data Management for Bio-Imaging. Questionnaire Data Report 1.0 Overview As part of the DMBI project an international meeting was organized around the project to bring together the bio-imaging community
A Brief History of the Microscope and its Significance in the Advancement of Biology and Medicine
Chapter 1 A Brief History of the Microscope and its Significance in the Advancement of Biology and Medicine This chapter provides a historical foundation of the field of microscopy and outlines the significant
Improved predictive modeling of white LEDs with accurate luminescence simulation and practical inputs
Improved predictive modeling of white LEDs with accurate luminescence simulation and practical inputs TracePro Opto-Mechanical Design Software s Fluorescence Property Utility TracePro s Fluorescence Property
Cytell Cell Imaging System
Cytell Cell Imaging System Simplify your cell analysis and start changing tomorrow today www.gelifesciences.com/cytell The Cytell Cell Imaging System is an intuitive cell analysis instrument that streamlines
Austin Peay State University Department of Chemistry Chem 1111. The Use of the Spectrophotometer and Beer's Law
Purpose To become familiar with using a spectrophotometer and gain an understanding of Beer s law and it s relationship to solution concentration. Introduction Scientists use many methods to determine
Leica TCS SP5 Confocal Laser Scanning Microscope User Guide 1. BASIC IMAGE ACQUISITION
Leica TCS SP5 Confocal Laser Scanning Microscope User Guide 1. BASIC IMAGE ACQUISITION This manual is the FIRST section of a THREE part Leica TCS - SP5 User Guide edited by Donald Pottle Leica True Confocal
Chapter 12 Filters for FISH Imaging
Chapter 12 Filters for FISH Imaging Dan Osborn The application of in situ hybridization (ISH) has advanced from short lived, non-specific isotopic methods, to very specific, long lived, multiple color
MIRAX SCAN The new way of looking at pathology
Microscopy from Carl Zeiss MIRAX SCAN The new way of looking at pathology Greater reliability. Greater efficiency. Virtual microscopy for research & analysis. Better. More efficient. Quality as the basis
Super Resolution Optical Microscopy. Bo Huang
Super Resolution Optical Microscopy Bo Huang Mar 30, 2012 0.1mm 10µm 1µm 100nm Naked eye: ~ 50 100 μm 1595, Zaccharias and Hans Janssen First microscope, 9x magnification Antony Van Leeuwenhoek (1632 1723),
COMPENSATION MIT Flow Cytometry Core Facility
COMPENSATION MIT Flow Cytometry Core Facility Why do we need compensation? 1) Because the long emission spectrum tail of dyes causes overlap like with the fluorophores FITC and PE. 2) For sensitivity reasons,
Chapter 13 Confocal Laser Scanning Microscopy C. Robert Bagnell, Jr., Ph.D., 2012
Chapter 13 Confocal Laser Scanning Microscopy C. Robert Bagnell, Jr., Ph.D., 2012 You are sitting at your microscope working at high magnification trying to sort out the three-dimensional compartmentalization
SILA Sistema Integrato di Laboratori per l Ambiente. CENTRE FOR MICROSCOPY AND MICROANALYSIS Scientific coordinator: Prof.ssa Rosanna De Rosa
CENTRE FOR MICROSCOPY AND MICROANALYSIS Scientific coordinator: Prof.ssa Rosanna De Rosa 0 The Centre for Microscopy and Microanalysis (CM2) is an interdisciplinary service centre, a comprehensive suite
Towards large dynamic range beam diagnostics and beam dynamics studies. Pavel Evtushenko
Towards large dynamic range beam diagnostics and beam dynamics studies Pavel Evtushenko Motivation Linacs with average current 1-2 ma and energy 1-2.5 GeV are envisioned as drivers for next generation
Realization of a UV fisheye hyperspectral camera
Realization of a UV fisheye hyperspectral camera Valentina Caricato, Andrea Egidi, Marco Pisani and Massimo Zucco, INRIM Outline Purpose of the instrument Required specs Hyperspectral technique Optical
Z-Stacking and Z-Projection using a Scaffold-based 3D Cell Culture Model
A p p l i c a t i o n N o t e Z-Stacking and Z-Projection using a Scaffold-based 3D Cell Culture Model Brad Larson and Peter Banks, BioTek Instruments, Inc., Winooski, VT Grant Cameron, TAP Biosystems
Nano-Spectroscopy. Solutions AFM-Raman, TERS, NSOM Chemical imaging at the nanoscale
Nano-Spectroscopy Solutions AFM-Raman, TERS, NSOM Chemical imaging at the nanoscale Since its introduction in the early 80 s, Scanning Probe Microscopy (SPM) has quickly made nanoscale imaging an affordable
http://dx.doi.org/10.1117/12.906346
Stephanie Fullerton ; Keith Bennett ; Eiji Toda and Teruo Takahashi "Camera simulation engine enables efficient system optimization for super-resolution imaging", Proc. SPIE 8228, Single Molecule Spectroscopy
Zecotek S Light Projection Network Marketing
White Paper Zecotek Visible Fiber Laser Platform Enabling the future of laser technology Zecotek Photonics Inc. (TSX- V: ZMS; Frankfurt: W1I) www.zecotek.com is a Canadian photonics technology company
Imaging and Bioinformatics Software
Imaging and Bioinformatics Software Software Overview 242 Gel Analysis Software 243 Ordering Information 246 Software Overview Software Overview See Also Imaging systems: pages 232 237. Bio-Plex Manager
5. Scanning Near-Field Optical Microscopy 5.1. Resolution of conventional optical microscopy
5. Scanning Near-Field Optical Microscopy 5.1. Resolution of conventional optical microscopy Resolution of optical microscope is limited by diffraction. Light going through an aperture makes diffraction
Programme PhD / Master course Advanced Microscopy and Vital Imaging 2014. Time Item Location 09.00 09.15 Welcome and brief overview of the course
Programme PhD / Master course Advanced Microscopy and Vital Imaging 2014 Monday, June 2, 2014 09.00 09.15 Welcome and brief overview of the course 09.15 10.00 Basics of Microscopy 10.15 12.45 Practical
Confocal Fluorescence Microscopy
Chapter 1 Confocal Fluorescence Microscopy 1.1 The principle Confocal fluorescence microscopy is a microscopic technique that provides true three-dimensional (3D) optical resolution. In microscopy, 3D
Simplicity. Reliability. Performance
Simplicity Reliability Performance ICP Without Compromise At Teledyne Leeman Labs atomic spectroscopy is our business, our only business. We are deeply committed to providing you with technically superior
Application Note. Single Cell PCR Preparation
Application Note Single Cell PCR Preparation From Automated Screening to the Molecular Analysis of Single Cells The AmpliGrid system is a highly sensitive tool for the analysis of single cells. In combination
Basic principles and mechanisms of NSOM; Different scanning modes and systems of NSOM; General applications and advantages of NSOM.
Lecture 16: Near-field Scanning Optical Microscopy (NSOM) Background of NSOM; Basic principles and mechanisms of NSOM; Basic components of a NSOM; Different scanning modes and systems of NSOM; General
Overview Image Acquisition of Microscopic Slides via Web Camera
MAX-PLANCK-INSTITUT FÜR MARINE MIKROBIOLOGIE ABTEILUNG MOLEKULARE ÖKOLOGIE Overview Image Acquisition of Microscopic Slides via Web Camera Andreas Ellrott and Michael Zeder Max Planck Institute for Marine
Make Life Easier by Using Modern Features of the SPCM Software
Make Life Easier by Using Modern Features of the SPCM Software Abstract. Over a long period of time the SPCM operating software of the Becker & Hickl TCSPC systems has continuously been upgraded with new
Advances in scmos Camera Technology Benefit Bio Research
Advances in scmos Camera Technology Benefit Bio Research scmos camera technology is gaining in popularity - Why? In recent years, cell biology has emphasized live cell dynamics, mechanisms and electrochemical
Product Range Overview
Product Range Overview Stereo Optical Inspection Microscopes Non-Contact Measurement Systems Laboratory Microscopes Metallurgical Microscopes FM 557119 Vision Engineering Ltd has been certificated for
AxioCam MRm Pure Sensitivity
Microscopy from Carl Zeiss AxioCam MRm Pure Sensitivity The New Standard for Digital Fluorescence Imaging AxioCam MRm from Carl Zeiss More Information at Low Light Intensities More than ever before, modern
AB SCIEX TOF/TOF 4800 PLUS SYSTEM. Cost effective flexibility for your core needs
AB SCIEX TOF/TOF 4800 PLUS SYSTEM Cost effective flexibility for your core needs AB SCIEX TOF/TOF 4800 PLUS SYSTEM It s just what you expect from the industry leader. The AB SCIEX 4800 Plus MALDI TOF/TOF
IncuCyte ZOOM Whole Well Imaging Overview
IncuCyte ZOOM Whole Well Imaging Overview With the release of the 2013B software, IncuCyte ZOOM users will have the added ability to image the complete surface of select multi-well plates and 35 mm dishes
Euro-BioImaging European Research Infrastructure for Imaging Technologies in Biological and Biomedical Sciences
Euro-BioImaging European Research Infrastructure for Imaging Technologies in Biological and Biomedical Sciences WP11 Data Storage and Analysis Task 11.1 Coordination Deliverable 11.2 Community Needs of
PROTOCOL. Immunostaining for Flow Cytometry. Background. Materials and equipment required.
PROTOCOL Immunostaining for Flow Cytometry 1850 Millrace Drive, Suite 3A Eugene, Oregon 97403 Rev.0 Background The combination of single cell analysis using flow cytometry and the specificity of antibody-based
Masters in Photonics and Optoelectronic Devices
Masters in Photonics and Optoelectronic Devices www.st-andrews.ac.uk/physics/msc The primary aim of this twelve-month, full-time is to provide specialist postgraduate training in modern optics and semiconductor
Inspection and Illumination Systems for Visual Quality Assurance. Large selection Attractive prices Tailored solutions. optometron.
Inspection and Illumination Systems for Visual Quality Assurance Large selection Attractive prices Tailored solutions optometron.de en Optometron fulfils a key role Visual quality assurance is essential
3D Raman Imaging Nearfield-Raman TERS. Solutions for High-Resolution Confocal Raman Microscopy. www.witec.de
3D Raman Imaging Nearfield-Raman TERS Solutions for High-Resolution Confocal Raman Microscopy www.witec.de 01 3D Confocal Raman Imaging Outstanding performance in speed, sensitivity, and resolution with
N-STORM. Super-resolution Microscope. Operation Manual
M605E 13.2.Nx.3 N-STORM Super-resolution Microscope Operation Manual (N-STORM Software Ver. 3.10) Introduction Introduction Thank you for purchasing a Nikon product. This instruction manual is written
Cary 100 Bio UV-Vis Operating Instructions 09/25/2012 S.V.
1234 Hach Hall 515-294-5805 www.cif.iastate.edu Cary 100 Bio UV-Vis Operating Instructions 09/25/2012 S.V. Location: Contact: 1240 Hach Hall Steve Veysey, 1234 Hach Hall Safety All researchers working
Coherence-controlled holographic microscopy for live-cell QPI
SPIE Photonics West February 2015 Coherence-controlled holographic microscopy for live-cell QPI Tomáš Slabý, Aneta Křížová, Martin Lošťák, Jana Čolláková, Pavel Kolman, Zbyněk Dostál, Lukáš Kvasnica, Martin
MiSeq: Imaging and Base Calling
MiSeq: Imaging and Page Welcome Navigation Presenter Introduction MiSeq Sequencing Workflow Narration Welcome to MiSeq: Imaging and. This course takes 35 minutes to complete. Click Next to continue. Please
Software-based three dimensional reconstructions and enhancements of focal depth in microphotographic images
FORMATEX 2007 A. Méndez-Vilas and J. Díaz (Eds.) Software-based three dimensional reconstructions and enhancements of focal depth in microphotographic images Jörg Piper Clinic Meduna, Department for Internal
The Basic Principle of Airyscanning. Technology Note
The Basic Principle of Airyscanning Technology Note The Basic Principle of Airyscanning Author: Klaus Weisshart Date: July 014 Airyscanning is a technique based on confocal laser scanning microscopy. We
Preface Light Microscopy X-ray Diffraction Methods
Preface xi 1 Light Microscopy 1 1.1 Optical Principles 1 1.1.1 Image Formation 1 1.1.2 Resolution 3 1.1.3 Depth of Field 5 1.1.4 Aberrations 6 1.2 Instrumentation 8 1.2.1 Illumination System 9 1.2.2 Objective
OPERATING INSTRUCTIONS Nikon TiE Deconvolution Microscope CCRB 1-220G
OPERATING INSTRUCTIONS Nikon TiE Deconvolution Microscope CCRB 1-220G Conventions Through these notes bold font refers to a software button and italics refer to a hardware switch. The software makes extensive
BIOSCIENCES COURSE TITLE AWARD
COURSE TITLE AWARD BIOSCIENCES As a Biosciences undergraduate student at the University of Westminster, you will benefit from some of the best teaching and facilities available. Our courses combine lecture,
2015 Training Courses
2015 Training Courses GDS, ICP-OES, Particle Size Analysis, C/S & O/N/H, S & Cl in Petroleum, X-Ray Fluorescence Exceeding Customer Expectations Training courses calendar 2015 HORIBA Scientific offers
High Definition Imaging
High Definition Imaging Scientific CMOS Camera Photon Technology International www.pti-nj.com Scientific CMOS Camera The new HDI camera is a breakthrough in scientific imaging cameras, due to its distinctive
