Spectral Imaging with the Opterra Multipoint Scanning Confocal

Size: px
Start display at page:

Download "Spectral Imaging with the Opterra Multipoint Scanning Confocal"

Transcription

1 Spectral Imaging with the Opterra Multipoint Scanning Confocal

2 Outline Opterra design overview Scan Modes Light Path Spectral Imaging with Opterra Drosophila larva heart.

3 Opterra Design Overview Supravideo rate, high speed slit scanner. Variable pinhole, linear array field scanner. EMCCD camera-based detector. High frequency scanning minimizes phototoxicity (due to very short dwell times).

4 Opterra Design Overview Multiple scan modes allow for optimization of resolution, speed and light delivery Linear pinhole/slit arrays (1-D) and separate light paths for emission and excitation minimize emission crosstalk

5 Aperture plate Emission Apertures Excitation Apertures

6 Opterra Aperture Positions Slit scanning positions 22 µm slit 35 µm slit 50 µm slit 70 µm slit 30 µm pinholes (x32) Field scanning positions 45 µm pinholes (x32) 60 µm pinholes (x32)

7 Opterra Imaging Scanner Light Path

8 Excitation Emission Excitation slits and pinholes

9 Scan Modes: Offering Flexibility and Optimization Airy disk: best focused spot a perfect lens can make For optimal resolution, want to match objective lens ability to create a focal point with pinhole size Optimization within experiments; Flexibility between experiments. Larger pinhole: more signal, cost of resolution Slits: more signal, faster scanning, cost of resolution in one dimension Ma g NA D Pinhole Slit

10 Illumination Shaping and Scanning Laser beam is shaped into a line, then scanned

11 Piezos move a fixed distance Time to move depends on exposure time It takes 2 frames for one complete piezo sweep Galvo moves a fixed distance Time to move depends on exposure time Galvo sweeps multiple cycles/frame, and piezos sweep only once per frame

12 Field-scanning combines multiple galvo sweeps with bidirectional piezo movement

13 Cross talk Linear pinhole arrangement: square root of crosstalk of 2-D array scanners. Provides improved axial resolution. Detector and microscope choices. Detector: High speed or high resolution. Microscope: Inverted or upright

14 Zebrafish Neurons 100 um Z Range

15 Tumor Slice: CFP and GFP 100 um Z range

16 EMCCDs are monochrome devices but color is often needed for visualization or discrimination of fluorophores

17 Traditional Approach Narrow bandpass filters How to detect hyperspectral (i.e. >3) colors without throwing away most of our signal!

18 The Amici Prism >95% Transmission at 630nm

19 4. Creates spectra from 32 lines on the sample CAMERA SENSOR 5. Shift all points by a row of pixels and repeat (16x) 2. Prism fans 32 points to 32 spectra 3. Galvanometer sweeps 32 points across the sample PINHOLE 1 PINHOLE Emission light from 32 pinholes enters prism

20 SFC Hyperspectral with amici 15 prism Color Frame Acquisition Each image captured is the full spectrum from 32 lines on the sample Between each exposure the 32 lines are shifted down by a row

21 Hyperspectral Stack Reconstruction

22

23 Component Analysis

24 Performance Analysis Negligible Noise Penalty vs. Regular Opterra image: - One exposure, one readout ms exposure time - one color Spectral Opterra SFC image: image: Exposures, readouts ms total exposure time - 15 color channels, integrated to one color false color image

25 Performance Analysis Spectral Resolution Invitrogen Green-Green Beads

26 Performance Analysis Spectral Resolution Mathieu Ducros, et al. Spectral Unmixing: Analysis of Performance in the Olfactory Bulb In Vivo. PLoS ONE. 2009; 4(2): e4418. doi: /journal.pone

27 Arabidopsis Root Arabidopsis Kaleidocell Root 60x Oil Objective Nuclei: EGFP Mitochondria: YFP Plastid: DSRed Plasma Membrane: GFP

28 Zebrafish Tail Tail of Zebrafish Embryo 40x Oil Objective Spinal Column (sox9b): EGFP Nerve cell surface: (GFAP) A568 Cell Body: Dapi

29 Frog Egg Mitosis Mitosis in Frog Eggs 60x Oil Objective Cell Membrane: mtag BFP Tubulin (spindles and membrane): egfp Histone (nuclei): mcherry

30 Spectral Montage: Whole Zebrafish

31 Zebrafish brain: Neural development

32 Dissected zebrafish head

33 Prairie View: Real Time Spectral Acquisition Selectable color bands for each image window. Real time update of spectral histogram. Multiple math modes Simple toggling between Spectral and Normal mode.

34 High Speed Spectral Acquisition 16 camera exposures for a full 15 channel spectral frame Leverages high speed scanning and high speed EMCCDs like the Photometrics Evolve Delta 512 x 512 sensor 15 channels spectral resolution > 4 Spectral frames per second 3/28/2014 Bruker Confidential 34

35 Advantages of the Opterra Spectra Negligible noise penalty 15 channel spectral resolution Facilitates multiple overlapping fluorophore separation High speed spectral capture Easily switchable between spectral and regular confocal modes Triple labeled zebrafish tail fin

Multidimensional Imaging with the Opterra Multipoint Scanning Confocal System

Multidimensional Imaging with the Opterra Multipoint Scanning Confocal System Multidimensional Imaging with the Opterra Multipoint Scanning Confocal System Outline Opterra design overview Light Path Scan Modes Performance Application data Drosophila larva heart. Courtesy of Nikon

More information

Opterra. Multipoint Scanning Confocal Microscope. Innovation with Integrity. Cell-Friendly, High-Speed, High-Resolution Imaging

Opterra. Multipoint Scanning Confocal Microscope. Innovation with Integrity. Cell-Friendly, High-Speed, High-Resolution Imaging Opterra Multipoint Scanning Confocal Microscope Cell-Friendly, High-Speed, High-Resolution Imaging Innovation with Integrity Fluorescence Microscopy Opterra Multipoint Scanning Confocal Microscope Superior

More information

Opterra II Multipoint Scanning Confocal Microscope. Innovation with Integrity

Opterra II Multipoint Scanning Confocal Microscope. Innovation with Integrity Opterra II Multipoint Scanning Confocal Microscope Enabling 4D Live-Cell Fluorescence Imaging through Speed, Sensitivity, Viability and Simplicity Innovation with Integrity Fluorescence Microscopy The

More information

Why and How? Daniel Gitler Dept. of Physiology Ben-Gurion University of the Negev. Microscopy course, Michmoret Dec 2005

Why and How? Daniel Gitler Dept. of Physiology Ben-Gurion University of the Negev. Microscopy course, Michmoret Dec 2005 Why and How? Daniel Gitler Dept. of Physiology Ben-Gurion University of the Negev Why use confocal microscopy? Principles of the laser scanning confocal microscope. Image resolution. Manipulating the

More information

Confocal Microscopy. (Increasing contrast and resolu6on using op6cal sec6oning) Lecture 7. November 2017

Confocal Microscopy. (Increasing contrast and resolu6on using op6cal sec6oning) Lecture 7. November 2017 Confocal Microscopy (Increasing contrast and resolu6on using op6cal sec6oning) Lecture 7 November 2017 3 Flavours of Microscope Confocal Laser Scanning Problem: Out of Focus Light Spinning disc 2-Photon

More information

1.The Problem LIGHT-LEVEL LEVEL IMAGING. light-level level Cameras. 3. Solutions. 2. Low-light LOW-LIGHT

1.The Problem LIGHT-LEVEL LEVEL IMAGING. light-level level Cameras. 3. Solutions. 2. Low-light LOW-LIGHT LOW-LIGHT LIGHT-LEVEL LEVEL IMAGING 1.The Problem 2. Low-light light-level level Cameras 3. Solutions How Much Light? I. Illumination system: 75 W Xenon Arc (~1mW/nm in visible) 490/10 nm exciter filter

More information

Rapid Adaptive Optical Recovery of Optimal Resolution over Large Volumes

Rapid Adaptive Optical Recovery of Optimal Resolution over Large Volumes SUPPLEMENTARY MATERIAL Rapid Adaptive Optical Recovery of Optimal Resolution over Large Volumes Kai Wang, Dan Milkie, Ankur Saxena, Peter Engerer, Thomas Misgeld, Marianne E. Bronner, Jeff Mumm, and Eric

More information

Leica Sp5 II Confocal User Guide

Leica Sp5 II Confocal User Guide Leica Sp5 II Confocal User Guide Turning on the Confocal System (instructions are posted in the room) 1. Turn on Laser Power Button 2. Turn Key to On position 3. Turn on Scanner Power Button 4. Turn on

More information

1 Set up the confocal light path for imaging a green dye (Alexa488-EGFP). For example, the

1 Set up the confocal light path for imaging a green dye (Alexa488-EGFP). For example, the 1 Set up the confocal light path for imaging a green dye (Alexa488-EGFP). For example, the light path as shown here using the 488 nm LASER (Laser Unit 1) reflecting off of the 405/488 nm Dichroic mirror

More information

LSM 510 META in Chang Gung University

LSM 510 META in Chang Gung University Content LSM 510 META in Chang ung University LSM 510 META 路 理 The features and applications of LSM 510 META 01-09 Introduction of the hardware 10-12 Fluorescence observation in conventional microscope

More information

Inside the LSM 880 NLO + Airyscan

Inside the LSM 880 NLO + Airyscan Inside the LSM 880 NLO + Airyscan Overview of the Newest High-End Point Scanning Solution from Carl Zeiss Microscopy Matt Curtis 3D Imaging Specialist John Dirnberger Account Manager Washington University

More information

Swept-Field User Guide

Swept-Field User Guide Swept-Field User Guide Note: for more details see the Prairie user manual at http://www.prairietechnologies.com/resources/software/prairieview.html Please report any problems to Julie Last (jalast@wisc.edu)

More information

Nature Methods: doi: /nmeth Supplementary Figure 1. Schematic of 2P-ISIM AO optical setup.

Nature Methods: doi: /nmeth Supplementary Figure 1. Schematic of 2P-ISIM AO optical setup. Supplementary Figure 1 Schematic of 2P-ISIM AO optical setup. Excitation from a femtosecond laser is passed through intensity control and shuttering optics (1/2 λ wave plate, polarizing beam splitting

More information

Basics of confocal imaging (part I)

Basics of confocal imaging (part I) Basics of confocal imaging (part I) Swiss Institute of Technology (EPFL) Faculty of Life Sciences Head of BIOIMAGING AND OPTICS BIOP arne.seitz@epfl.ch Lateral resolution BioImaging &Optics Platform Light

More information

BASICS OF CONFOCAL IMAGING (PART I)

BASICS OF CONFOCAL IMAGING (PART I) BASICS OF CONFOCAL IMAGING (PART I) INTERNAL COURSE 2012 LIGHT MICROSCOPY Lateral resolution Transmission Fluorescence d min 1.22 NA obj NA cond 0 0 rairy 0.61 NAobj Ernst Abbe Lord Rayleigh Depth of field

More information

Travel to New Dimensions- LSM 880. The Resolution of a Microscope is limited. The Resolution of a Microscope is limited. Image. Image. Object.

Travel to New Dimensions- LSM 880. The Resolution of a Microscope is limited. The Resolution of a Microscope is limited. Image. Image. Object. Travel to New Dimensions- LSM 880 LSM 880: The Power of Sensitivity Our Latest Member of the LSM 880 with GaAsP Detectors Sensitivity, and Ease of Use Innovative High-End Laser Scanning Microscopes from

More information

Nature Methods: doi: /nmeth Supplementary Figure 1. Comparison of HySP and linear unmixing under different signal-to-noise ratios (SNRs).

Nature Methods: doi: /nmeth Supplementary Figure 1. Comparison of HySP and linear unmixing under different signal-to-noise ratios (SNRs). Supplementary Figure 1 Comparison of HySP and linear unmixing under different signal-to-noise ratios (SNRs). (a) TrueColor images of 32 channel datasets of zebrafish labeled with H2B-Cerulean, kdrl:egfp,

More information

Multifluorescence The Crosstalk Problem and Its Solution

Multifluorescence The Crosstalk Problem and Its Solution Multifluorescence The Crosstalk Problem and Its Solution If a specimen is labeled with more than one fluorochrome, each image channel should only show the emission signal of one of them. If, in a specimen

More information

Components of confocal and two-photon microscopes

Components of confocal and two-photon microscopes Components of confocal and two-photon microscopes Internal training 07/04/2016 A. GRICHINE Platform Optical microscopy Cell imaging, IAB, ISdV Plan Confocal laser scanning microscope o o o Principle Main

More information

Confocal imaging on the Leica TCS SP8. 1) Turn the system on. 2) Use TCS user account. 3) Start LAS X software:

Confocal imaging on the Leica TCS SP8. 1) Turn the system on. 2) Use TCS user account. 3) Start LAS X software: Confocal imaging on the Leica TCS SP8 1) Turn the system on. 2) Use TCS user account. 3) Start LAS X software: 4) Do not touch the microscope while the software is initializing. Choose your options: Turn

More information

Nature Methods: doi: /nmeth Supplementary Figure 1

Nature Methods: doi: /nmeth Supplementary Figure 1 . Supplementary Figure 1 Schematics and characterization of our AO two-photon fluorescence microscope. (a) Essential components of our AO two-photon fluorescence microscope: Ti:Sapphire laser; optional

More information

Boulevard du Temple Daguerrotype (Paris,1838) a busy street? Nyquist sampling for movement

Boulevard du Temple Daguerrotype (Paris,1838) a busy street? Nyquist sampling for movement Boulevard du Temple Daguerrotype (Paris,1838) a busy street? Nyquist sampling for movement CONFOCAL MICROSCOPY BioVis Uppsala, 2017 Jeremy Adler Matyas Molnar Dirk Pacholsky Widefield & Confocal Microscopy

More information

Practical work no. 3: Confocal Live Cell Microscopy

Practical work no. 3: Confocal Live Cell Microscopy Practical work no. 3: Confocal Live Cell Microscopy Course Instructor: Mikko Liljeström (MIU) 1 Background Confocal microscopy: The main idea behind confocality is that it suppresses the signal outside

More information

長庚大學共軛焦顯微鏡課程 長庚大學共軛焦顯微鏡課程. Spot light 長庚大學

長庚大學共軛焦顯微鏡課程 長庚大學共軛焦顯微鏡課程. Spot light 長庚大學 長庚大學共軛焦顯微鏡課程 Spot light 長庚大學共軛焦顯微鏡課程 20071030 長庚大學 Basic principle of Laser Scanning Confocal Microscopy The application of LSM 510 META detector Multiphoton microscopy basic principle and introduction

More information

Life Science Instrumentation. New Generation. Light Sheet Fluorescence Microscope. Alph

Life Science Instrumentation. New Generation. Light Sheet Fluorescence Microscope. Alph Life Science Instrumentation Light Sheet Fluorescence Microscope New Generation Alph Modular Light Sheet Microscope Alpha 3 is a new generation of light sheet fluorescence microscope addressing the needs

More information

Training Guide for Carl Zeiss LSM 5 LIVE Confocal Microscope

Training Guide for Carl Zeiss LSM 5 LIVE Confocal Microscope Training Guide for Carl Zeiss LSM 5 LIVE Confocal Microscope AIM 4.2 Optical Imaging & Vital Microscopy Core Baylor College of Medicine (2017) Power ON Routine 1 2 Verify that main power switches on the

More information

Quick Guide for Zeiss 710 Laser Scanning Confocal MGH Cancer Center

Quick Guide for Zeiss 710 Laser Scanning Confocal MGH Cancer Center Quick Guide for Zeiss 710 Laser Scanning Confocal MGH Cancer Center For any questions or concerns, please contact: Linda Nieman lnieman@mgh.harvard.edu Office: (617) 643-9684 Cell: (512) 565-8076 Chenyue

More information

Topics. - How to calibrate the LSM scanner. - How to clean the microscope. - How to adjust the pinhole alignment. - How to adjust the Collimator

Topics. - How to calibrate the LSM scanner. - How to clean the microscope. - How to adjust the pinhole alignment. - How to adjust the Collimator Topics - How to calibrate the LSM scanner - How to measure the PSF - How to clean the microscope - How to adjust the pinhole alignment - How to adjust the Collimator How to calibrate the LSM scanner The

More information

Confocal Microscopy. Kristin Jensen

Confocal Microscopy. Kristin Jensen Confocal Microscopy Kristin Jensen 17.11.05 References Cell Biological Applications of Confocal Microscopy, Brian Matsumoto, chapter 1 Studying protein dynamics in living cells,, Jennifer Lippincott-Schwartz

More information

Nikon AZ100. Laser Scanning Macro Confocal Microscope. Jordan Briscoe Adam Fries Kyle Marchuk Kaitlin Corbin. May 2017.

Nikon AZ100. Laser Scanning Macro Confocal Microscope. Jordan Briscoe Adam Fries Kyle Marchuk Kaitlin Corbin. May 2017. Nikon AZ100 Laser Scanning Macro Confocal Microscope Jordan Briscoe Adam Fries Kyle Marchuk Kaitlin Corbin May 2017 Contents 1 Introduction 2 2 Hardware - Startup 2 3 Software/Operation 4 3.1 Multidimensional

More information

Point Spread Function. Confocal Laser Scanning Microscopy. Confocal Aperture. Optical aberrations. Alternative Scanning Microscopy

Point Spread Function. Confocal Laser Scanning Microscopy. Confocal Aperture. Optical aberrations. Alternative Scanning Microscopy Bi177 Lecture 5 Adding the Third Dimension Wide-field Imaging Point Spread Function Deconvolution Confocal Laser Scanning Microscopy Confocal Aperture Optical aberrations Alternative Scanning Microscopy

More information

Multicolor 4D Fluorescence Microscopy using Ultrathin Bessel Light sheets

Multicolor 4D Fluorescence Microscopy using Ultrathin Bessel Light sheets SUPPLEMENTARY MATERIAL Multicolor 4D Fluorescence Microscopy using Ultrathin Bessel Light sheets Teng Zhao, Sze Cheung Lau, Ying Wang, Yumian Su, Hao Wang, Aifang Cheng, Karl Herrup, Nancy Y. Ip, Shengwang

More information

Quick Start Guide. Leica SP5 X

Quick Start Guide. Leica SP5 X Quick Start Guide Leica SP5 X Please note: Some of the information in this guide was taken from Leica Microsystems Leica TCS SP5 LAS AF Guide for New Users. This work is licensed under the Creative Commons

More information

Leica TCS SP8 Quick Start Guide

Leica TCS SP8 Quick Start Guide Leica TCS SP8 Quick Start Guide Leica TCS SP8 System Overview Start-Up Procedure 1. Turn on the CTR Control Box, EL6000 fluorescent light source for the microscope stand. 2. Turn on the Scanner Power

More information

LSM 710 Confocal Microscope Standard Operation Protocol

LSM 710 Confocal Microscope Standard Operation Protocol LSM 710 Confocal Microscope Standard Operation Protocol Basic Operation Turning on the system 1. Switch on Main power switch 2. Switch on System / PC power button 3. Switch on Components power button 4.

More information

Quick Guide for Zeiss 710 Laser Scanning Confocal MGH Cancer Center

Quick Guide for Zeiss 710 Laser Scanning Confocal MGH Cancer Center Quick Guide for Zeiss 710 Laser Scanning Confocal MGH Cancer Center For any questions or concerns, please contact: Linda Nieman lnieman@mgh.harvard.edu Office: (617) 643-9684 Cell: (512) 565-8076 Chenyue

More information

Bi/BE 227 Winter Assignment #3. Adding the third dimension: 3D Confocal Imaging

Bi/BE 227 Winter Assignment #3. Adding the third dimension: 3D Confocal Imaging Bi/BE 227 Winter 2016 Assignment #3 Adding the third dimension: 3D Confocal Imaging Schedule: Jan 20: Assignment Jan 20-Feb 8: Work on assignment Feb 10: Student PowerPoint presentations. Goals for this

More information

Supplemental Method Information Zeiss LSM710

Supplemental Method Information Zeiss LSM710 Supplemental Method Information Zeiss LSM710 1 Under the Light Path window set up the confocal for imaging a green dye (Alexa488-EGFP). For example, set up the light path as shown here using the 488 nm

More information

TRAINING MANUAL. Olympus FV1000

TRAINING MANUAL. Olympus FV1000 TRAINING MANUAL Olympus FV1000 September 2014 TABLE OF CONTENTS A. Start-Up Procedure... 1 B. Visual Observation under the Microscope... 1 C. Image Acquisition... 4 A brief Overview of the Settings...

More information

Last updated: May 2014 Y.DeGraaf

Last updated: May 2014 Y.DeGraaf FLINDERS MICROSCOPY BIOMEDICAL SERVICES AVAILABLE MICROSCOPES AND SPECIFICATIONS & INFORMATION REGARDING TRAINING FOR NEW USERS Last updated: May 2014 Y.DeGraaf If you have new staff or students (Honours/Masters

More information

Shreyash Tandon M.S. III Year

Shreyash Tandon M.S. III Year Shreyash Tandon M.S. III Year 20091015 Confocal microscopy is a powerful tool for generating high-resolution images and 3-D reconstructions of a specimen by using point illumination and a spatial pinhole

More information

Zeiss 880 Training Notes Zen 2.3

Zeiss 880 Training Notes Zen 2.3 Zeiss 880 Training Notes Zen 2.3 1 Turn on the HXP 120V Lamp 2 Turn on Main Power Switch Turn on the Systems PC Switch Turn on the Components Switch. 3 4 5 Turn on the PC and log into your account. Start

More information

Final Exam, 150 points PMB 185: Techniques in Light Microscopy

Final Exam, 150 points PMB 185: Techniques in Light Microscopy Final Exam, 150 points Name PMB 185: Techniques in Light Microscopy Point value is in parentheses at the end of each question. Note: GFP = green fluorescent protein ; CFP = cyan fluorescent protein ; YFP

More information

Imaging Beyond the Basics: Optimizing Settings on the Leica SP8 Confocal

Imaging Beyond the Basics: Optimizing Settings on the Leica SP8 Confocal Imaging Beyond the Basics: Optimizing Settings on the Leica SP8 Confocal Todays Goal: Introduce some additional functionalities of the Leica SP8 confocal HyD vs. PMT detectors Dye Assistant Scanning By

More information

Bio 407. Applied microscopy. Introduction into light microscopy. José María Mateos. Center for Microscopy and Image Analysis

Bio 407. Applied microscopy. Introduction into light microscopy. José María Mateos. Center for Microscopy and Image Analysis Center for Microscopy and Image Analysis Bio 407 Applied Introduction into light José María Mateos Fundamentals of light Compound microscope Microscope composed of an objective and an additional lens (eyepiece,

More information

Imaging Retreat - UMASS Customized real-time confocal and 2-photon imaging

Imaging Retreat - UMASS Customized real-time confocal and 2-photon imaging Imaging Retreat - UMASS 2012 Customized real-time confocal and 2-photon imaging Mike Sanderson Department of Microbiology and Physiological Systems University of Massachusetts Medical School Thanks for

More information

Confocal, hyperspectral, spinning disk

Confocal, hyperspectral, spinning disk Confocal, hyperspectral, spinning disk Administrative HW 6 due on Fri Midterm on Wed Covers everything since previous midterm 8.5 x 11 sheet allowed, 1 side Guest lecture by Joe Dragavon on Mon 10/30 Last

More information

LSM 780 Confocal Microscope Standard Operation Protocol

LSM 780 Confocal Microscope Standard Operation Protocol LSM 780 Confocal Microscope Standard Operation Protocol Basic Operation Turning on the system 1. Sign on log sheet according to Actual start time 2. Check Compressed Air supply for the air table 3. Switch

More information

Technology Note ZEISS LSM 880 with Airyscan

Technology Note ZEISS LSM 880 with Airyscan Technology Note ZEISS LSM 880 with Airyscan Introducing the Fast Acquisition Mode ZEISS LSM 880 with Airyscan Introducing the Fast Acquisition Mode Author: Dr. Annette Bergter Carl Zeiss Microscopy GmbH,

More information

Instant super-resolution imaging in live cells and embryos via analog image processing

Instant super-resolution imaging in live cells and embryos via analog image processing Nature Methods Instant super-resolution imaging in live cells and embryos via analog image processing Andrew G. York, Panagiotis Chandris, Damian Dalle Nogare, Jeffrey Head, Peter Wawrzusin, Robert S.

More information

The DCS-120 Confocal Scanning FLIM System

The DCS-120 Confocal Scanning FLIM System he DCS-120 Confocal Scanning FLIM System he bh DCS-120 confocal scanning FLIM system converts a conventional microscope into a high-performance fluorescence lifetime imaging system. he system is based

More information

ADVANCED METHODS FOR CONFOCAL MICROSCOPY II. Jean-Yves Chatton Sept. 2006

ADVANCED METHODS FOR CONFOCAL MICROSCOPY II. Jean-Yves Chatton Sept. 2006 ADVANCED METHODS FOR CONFOCAL MICROSCOPY II Jean-Yves Chatton Sept. 2006 Workshop outline Confocal microscopy of living cells and tissues X-Z scanning Time series Bleach: FRAP, photoactivation Emission

More information

More fancy SPIM, Even fancier SPIM

More fancy SPIM, Even fancier SPIM More fancy SPIM, Even fancier SPIM Last class Light sheet microscopy Fancy SPIM (ispim, dspim, etc ) This class Multi camera SPIM SIM SPIM Bessels d x,y = λ em 2 NA d z = 2 NA λ ex + n(1 cosθ λ em 1 IsoView

More information

The Zeiss AiryScan System, Confocal Four.

The Zeiss AiryScan System, Confocal Four. The Zeiss AiryScan System, Confocal Four. Overview. The Zeiss AiryScan module is a segmented, radially stacked GaASP detector and collector system designed to subsample the airy disk of a point emission

More information

Comparing FCS and FRAP as methodologies for calculating diffusion

Comparing FCS and FRAP as methodologies for calculating diffusion Bi/BE 227 Winter 2018 Assignment #4 Comparing FCS and FRAP as methodologies for calculating diffusion Schedule: Jan 29: Assignment Jan 29-Feb 14: Work on assignment Feb 14: Student PowerPoint presentations.

More information

Microscopy from Carl Zeiss

Microscopy from Carl Zeiss Microscopy from Carl Zeiss Contents Page Contents... 1 Introduction... 1 Starting the System... 2 Introduction to ZEN Efficient Navigation... 5 Setting up the microscope... 10 Configuring the beam path

More information

Leica TCS SP8 Quick Start Guide

Leica TCS SP8 Quick Start Guide Leica TCS SP8 Quick Start Guide Leica TCS SP8 System Overview Start-Up Procedure 1. Turn on the CTR Control Box, Fluorescent Light for the microscope stand. 2. Turn on the Scanner Power (1) on the front

More information

Fast, high-contrast imaging of animal development with scanned light sheet based structured-illumination microscopy

Fast, high-contrast imaging of animal development with scanned light sheet based structured-illumination microscopy nature methods Fast, high-contrast imaging of animal development with scanned light sheet based structured-illumination microscopy Philipp J Keller, Annette D Schmidt, Anthony Santella, Khaled Khairy,

More information

Dynamic Confocal Imaging of Living Brain. Advantages and risks of multiphoton microscopy in physiology

Dynamic Confocal Imaging of Living Brain. Advantages and risks of multiphoton microscopy in physiology Dynamic Confocal Imaging of Living Brain Advantages and risks of multiphoton microscopy in physiology Confocal laser scanning microscopy In conventional optical microscopy focused and out-offocus light

More information

Things to check before start-up.

Things to check before start-up. Byeong Cha Page 1 11/24/2009 Manual for Leica SP2 Confocal Microscope Enter you name, the date, the time, and the account number in the user log book. Things to check before start-up. Make sure that your

More information

Multicolor two-photon light-sheet microscopy Pierre Mahou, Julien Vermot, Emmanuel Beaurepaire & Willy Supatto

Multicolor two-photon light-sheet microscopy Pierre Mahou, Julien Vermot, Emmanuel Beaurepaire & Willy Supatto Mahou et al Supplementary Information Page 1 / 16 Multicolor two-photon light-sheet microscopy Pierre Mahou, Julien Vermot, Emmanuel Beaurepaire & Willy Supatto SUPPLEMENTAR INFORMATION SUPPLEMENTAR ITEM

More information

Leica TCS SL Confocal Training. Neuroscience Imaging Core Staff. Core Director. Facility Manager

Leica TCS SL Confocal Training. Neuroscience Imaging Core Staff. Core Director. Facility Manager Leica TCS SL Confocal Training Neuroscience Imaging Facility The Ohio State University Rightmire Hall 614-292-1367 Staff Core Director Anthony Brown, Ph. D. 060 Rightmire Hall 614-292-1205 brown.2302@osu.edu

More information

ZEISS LSM510META confocal manual

ZEISS LSM510META confocal manual ZEISS LSM510META confocal manual Switching on the system 1) Switch on the Remote Control button located on the table to the right of the microscope. This is the main switch for the whole system including

More information

Exam 4. Name: Class: Date: Multiple Choice Identify the choice that best completes the statement or answers the question.

Exam 4. Name: Class: Date: Multiple Choice Identify the choice that best completes the statement or answers the question. Name: Class: Date: Exam 4 Multiple Choice Identify the choice that best completes the statement or answers the question. 1. Mirages are a result of which physical phenomena a. interference c. reflection

More information

3 Choose the Channels button and set the Channel Settings. Set the Pinhole to 1 Airy unit.

3 Choose the Channels button and set the Channel Settings. Set the Pinhole to 1 Airy unit. 1 Set up the confocal light path for imaging a green dye (e.g. Alexa488-EGFP). For example, under the Configuration Control window the light path could be set up as shown here using the 488 nm LASER (found

More information

Introduction to light microscopy

Introduction to light microscopy Center for Microscopy and Image Anaylsis Introduction to light Imaging with light / Overview of techniques Urs Ziegler ziegler@zmb.uzh.ch Light interacting with matter Absorbtion Refraction Diffraction

More information

Training Guide for Carl Zeiss LSM 510 META Confocal Microscope

Training Guide for Carl Zeiss LSM 510 META Confocal Microscope Training Guide for Carl Zeiss LSM 510 META Confocal Microscope AIM 4.2 Optical Imaging & Vital Microscopy Core Baylor College of Medicine (2017) Power ON Routine 1 2 Turn ON Components and System/PC switches

More information

Light Microscopy. Upon completion of this lecture, the student should be able to:

Light Microscopy. Upon completion of this lecture, the student should be able to: Light Light microscopy is based on the interaction of light and tissue components and can be used to study tissue features. Upon completion of this lecture, the student should be able to: 1- Explain the

More information

3D light microscopy techniques

3D light microscopy techniques 3D light microscopy techniques The image of a point is a 3D feature In-focus image Out-of-focus image The image of a point is not a point Point Spread Function (PSF) 1D imaging 1 1 2! NA = 0.5! NA 2D imaging

More information

1 Co Localization and Working flow with the lsm700

1 Co Localization and Working flow with the lsm700 1 Co Localization and Working flow with the lsm700 Samples -1 slide = mousse intestine, Dapi / Ki 67 with Cy3/ BrDU with alexa 488. -1 slide = mousse intestine, Dapi / Ki 67 with Cy3/ no BrDU (but with

More information

VivaTome. Discover the Dynamics of Life. The Entry-level System that Captures Dynamic Processes with Outstanding Image Quality.

VivaTome. Discover the Dynamics of Life. The Entry-level System that Captures Dynamic Processes with Outstanding Image Quality. Microscopy from Carl Zeiss VivaTome Discover the Dynamics of Life The Entry-level System that Captures Dynamic Processes with Outstanding Image Quality. Innovative Technology Captures Dynamic Processes

More information

Guide to Confocal 5. Starting session

Guide to Confocal 5. Starting session Guide to Confocal 5 Remember that when booking and before starting session you can check for any problems at https://www.bris.ac.uk/biochemistry/uobonly/cif/index.html Starting session Switch on microscope

More information

Training Guide for Carl Zeiss LSM 880 with AiryScan FAST

Training Guide for Carl Zeiss LSM 880 with AiryScan FAST Training Guide for Carl Zeiss LSM 880 with AiryScan FAST ZEN 2.3 Optical Imaging & Vital Microscopy Core Baylor College of Medicine (2018) Power ON Routine 1 2 Turn ON Main Switch from the remote control

More information

Nikon C1si Spectral Laser Scanning Confocal Microscope. User Guide

Nikon C1si Spectral Laser Scanning Confocal Microscope. User Guide Nikon C1si Spectral Laser Scanning Confocal Microscope User Guide Contents: C1Si Turn-On/ShutDown Procedures... 2 Overview... 4 Setup for epi-illumination to view through the eyepieces:... 5 Setup for

More information

Zeiss 780 Training Notes

Zeiss 780 Training Notes Zeiss 780 Training Notes Turn on Main Switch, System PC and Components Switches 780 Start up sequence Do you need the argon laser (458, 488, 514 nm lines)? Yes Turn on the laser s main power switch and

More information

FEMTOSMART. Benefits. Features

FEMTOSMART. Benefits. Features FEMTOSMART Extremely large space under the objective For in vivo studies Field upgradability Patented imaging technologies Flexible scanning methods Maximal photon collection Elevated, column-based body

More information

Microscope Confocal Sp2 Upright.

Microscope Confocal Sp2 Upright. Microscope Confocal Sp2 Upright. Welcome to the Leica Sp2 Confocal Upright tutorial. Before using the Sp2 Invert, You will need to put down your name on the reservation system = http://svintranet.epfl.ch/index.php?optio

More information

Supplemental Figure 1: Histogram of 63x Objective Lens z axis Calculated Resolutions. Results from the MetroloJ z axis fits for 5 beads from each

Supplemental Figure 1: Histogram of 63x Objective Lens z axis Calculated Resolutions. Results from the MetroloJ z axis fits for 5 beads from each Supplemental Figure 1: Histogram of 63x Objective Lens z axis Calculated Resolutions. Results from the MetroloJ z axis fits for 5 beads from each lens with a 1 Airy unit pinhole setting. Many water lenses

More information

Deep and fast live imaging with two-photon scanned light-sheet microscopy

Deep and fast live imaging with two-photon scanned light-sheet microscopy Nature Methods Deep and fast live imaging with two-photon scanned light-sheet microscopy Thai V Truong, Willy Supatto, Davis S Koos, John M Choi & Scott E Fraser Supplementary Figure 1 Supplementary Figure

More information

Training Guide for Leica SP8 Confocal/Multiphoton Microscope

Training Guide for Leica SP8 Confocal/Multiphoton Microscope Training Guide for Leica SP8 Confocal/Multiphoton Microscope LAS AF v3.3 Optical Imaging & Vital Microscopy Core Baylor College of Medicine (2017) Power ON Routine 1 2 Turn ON power switch for epifluorescence

More information

Application Note. The New 2D Superresolution Mode for ZEISS Airyscan 120 nm Lateral Resolution without Acquiring a Z-stack

Application Note. The New 2D Superresolution Mode for ZEISS Airyscan 120 nm Lateral Resolution without Acquiring a Z-stack The New 2D Superresolution Mode for ZEISS Airyscan 120 nm Lateral Resolution without Acquiring a Z-stack The New 2D Superresolution Mode for ZEISS Airyscan 120 nm Lateral Resolution without Acquiring a

More information

A 3D Multi-Aperture Image Sensor Architecture

A 3D Multi-Aperture Image Sensor Architecture A 3D Multi-Aperture Image Sensor Architecture Keith Fife, Abbas El Gamal and H.-S. Philip Wong Department of Electrical Engineering Stanford University Outline Multi-Aperture system overview Sensor architecture

More information

EUV microscopy - a user s perspective Dimitri Scholz EUV,

EUV microscopy - a user s perspective Dimitri Scholz EUV, EUV microscopy - a user s perspective Dimitri Scholz EUV, 09.11.2011 Imaging technologies: available at UCD now and in the next future Begin ab ovo - Simple approaches direct to the goal - Standard methods

More information

ANSWER KEY Lab 2 (IGB): Bright Field and Fluorescence Optical Microscopy and Sectioning

ANSWER KEY Lab 2 (IGB): Bright Field and Fluorescence Optical Microscopy and Sectioning Phys598BP Spring 2016 University of Illinois at Urbana-Champaign ANSWER KEY Lab 2 (IGB): Bright Field and Fluorescence Optical Microscopy and Sectioning Location: IGB Core Microscopy Facility Microscope:

More information

Figure S1 Figure S1. Wild type IgG and FcRn colocalize in APPL+ TCs.

Figure S1 Figure S1. Wild type IgG and FcRn colocalize in APPL+ TCs. Figure S1 Figure S1. Wild type IgG and FcRn colocalize in APPL+ TCs. HMEC-1 cells were cotransfected with GFP-FcRn and β2m. Transfected cells were incubated with 200 μg/ml Alexa 647-wild type IgG (A) or

More information

3. are adherent cells (ie. cells in suspension are too far away from the coverslip)

3. are adherent cells (ie. cells in suspension are too far away from the coverslip) Before you begin, make sure your sample... 1. is seeded on #1.5 coverglass (thickness = 0.17) 2. is an aqueous solution (ie. fixed samples mounted on a slide will not work - not enough difference in refractive

More information

Operating Instructions for Zeiss LSM 510

Operating Instructions for Zeiss LSM 510 Operating Instructions for Zeiss LSM 510 Location: GNL 6.312q (BSL3) Questions? Contact: Maxim Ivannikov, maivanni@utmb.edu 1 Attend A Complementary Training Before Using The Microscope All future users

More information

Fundamentals of Light Microscopy II: Fluorescence, Deconvolution, Confocal, Multiphoton, Spectral microscopy. Integrated Microscopy Course

Fundamentals of Light Microscopy II: Fluorescence, Deconvolution, Confocal, Multiphoton, Spectral microscopy. Integrated Microscopy Course Fundamentals of Light Microscopy II: Fluorescence, Deconvolution, Confocal, Multiphoton, Spectral microscopy Integrated Microscopy Course Review Lecture 1: Microscopy Basics Light train Kohler illumination*

More information

Nasmyth Ultraview Vox User Protocol

Nasmyth Ultraview Vox User Protocol Nasmyth Ultraview Vox User Protocol Switch on all wall sockets labelled Nasmyth, switch camera on (power supply located on table behind monitor), switch on laser switch in laser rack, switch computer on

More information

We attempted to separate the two dyes by acquiring images using a single excitation wavelength and just two emission wavelengths.

We attempted to separate the two dyes by acquiring images using a single excitation wavelength and just two emission wavelengths. TN437: Spectral Separation of monochrome images using Volocity 4.0 Introduction Spectral Separation is a technique that allows the user to separate images containing data from more than one fluorochrome

More information

WHITE PAPER FAST PROTEIN INTERACTION BINDING CURVES WITH INO S F-HS CONFOCAL MICROSCOPE

WHITE PAPER FAST PROTEIN INTERACTION BINDING CURVES WITH INO S F-HS CONFOCAL MICROSCOPE WHITE PAPER FAST PROTEIN INTERACTION BINDING CURVES WITH INO S F-HS CONFOCAL MICROSCOPE Christian Tardif, Jean-Pierre Bouchard Pascal Gallant, Sebastien Roy, Ozzy Mermut September 2017 Introduction Protein-protein

More information

3D light microscopy techniques

3D light microscopy techniques 3D light microscopy techniques The image of a point is a 3D feature In-focus image Out-of-focus image The image of a point is not a point Point Spread Function (PSF) 1D imaging 2D imaging 3D imaging Resolution

More information

Resolution. Diffraction from apertures limits resolution. Rayleigh criterion θ Rayleigh = 1.22 λ/d 1 peak at 2 nd minimum. θ f D

Resolution. Diffraction from apertures limits resolution. Rayleigh criterion θ Rayleigh = 1.22 λ/d 1 peak at 2 nd minimum. θ f D Microscopy Outline 1. Resolution and Simple Optical Microscope 2. Contrast enhancement: Dark field, Fluorescence (Chelsea & Peter), Phase Contrast, DIC 3. Newer Methods: Scanning Tunneling microscopy (STM),

More information

Fastest high definition Raman imaging. Fastest Laser Raman Microscope RAMAN

Fastest high definition Raman imaging. Fastest Laser Raman Microscope RAMAN Fastest high definition Raman imaging Fastest Laser Raman Microscope RAMAN - 11 www.nanophoton.jp Observation A New Generation in Raman Observation RAMAN-11 developed by Nanophoton was newly created by

More information

Title: Leica SP5 Confocal User Manual

Title: Leica SP5 Confocal User Manual Title: Leica SP5 Confocal User Manual Date of first issue: 23/10/2015 Date of review: Version: Admin For assistance or to report an issue Office: CG07 or 05 Email: Igmm-imaginghelpdesk@igmm.ed.ac.uk Website:

More information

Nikon Eclipse Ti2-E Widefield/Spinning Disk Confocal Microscope Standard Operation Protocol

Nikon Eclipse Ti2-E Widefield/Spinning Disk Confocal Microscope Standard Operation Protocol Nikon Eclipse Ti-E Widefield/Spinning Disk Confocal Microscope Standard Operation Protocol Please sign on the log sheet before switching on system. Turn on system Turn on A only if confocal mode or laser

More information

Fast Laser Raman Microscope RAMAN

Fast Laser Raman Microscope RAMAN Fast Laser Raman Microscope RAMAN - 11 www.nanophoton.jp Fast Raman Imaging A New Generation of Raman Microscope RAMAN-11 developed by Nanophoton was created by combining confocal laser microscope technology

More information

Enhancement of the lateral resolution and the image quality in a line-scanning tomographic optical microscope

Enhancement of the lateral resolution and the image quality in a line-scanning tomographic optical microscope Summary of the PhD thesis Enhancement of the lateral resolution and the image quality in a line-scanning tomographic optical microscope Author: Dudás, László Supervisors: Prof. Dr. Szabó, Gábor and Dr.

More information

Confocal Microscope. Confocal Microscope C2

Confocal Microscope. Confocal Microscope C2 Confocal Microscope Confocal Microscope C2 Confocal Microscope An essential microscopy laboratory instrument The C2 confocal microscope system comprises a new generation of Nikon confocal instruments designed

More information

Operating Checklist for using the Laser Scanning Confocal Microscope. Leica TCS SP5.

Operating Checklist for using the Laser Scanning Confocal Microscope. Leica TCS SP5. Smith College August 2010 Operating Checklist for using the Laser Scanning Confocal Microscope Leica TCS SP5. CONTENT, page no. Startup, 1 Initial set-up, 1 Software, 2 Microscope Specimen observation

More information