Welcome!
News & Status
Facility Map
People
Equipment Issues
Contact Us
Overview
Facility Operations
Network & Computers
Fluoresc. & Confocal
Electron Microscopy
Immuno-EM
Overview
Requesting Projects
Application Forms
Preparatory Checklist
Why Join?
Rules for Members
Application Forms
User Fees
Reservations
Member Rules
Manuals & Tutorials
User Fees
Overview
Other Links
Gallery
Microscope Facility
All of Hopkins
News & Status
2008-08-11
Wood Basic Science Bldg POWER OUTAGE (8/11-8/12)
2008-08-11
Wood Basic Science Bldg POWER OUTAGE (8/11-8/12)
2008-08-07
Physiology Building Power Outage 8/8-8/11
Staff Position Open &
Research Opportunities
Main List of Frequently Asked Questions
General Questions & Facility Operations FAQ
Where is the Facility located? How do I get there?
How do I schedule an appointment for consultation?
(Casual drop-in visits are always welcome!)
Who can use the Facility?
Do I need to be a member to use the Facility?
What is membership? Why should I join?
Will the Facility staff help me use Facility equipment?
Can I use Facility equipment myself?
Will the Facility staff help prepare specimens and collect images?
Will the Facility staff help me analyze my data?
Will the Facility staff help me customize equipment or software for my applications?
Will the Facility purchase new equipment or accessories for my applications?
Can Facility staff collaborate with me on my microscopy project?
Network & Information Technology FAQ
How can I access my images from outside School of Medicine?
How do I get to the Microscope Facility Server?
I've forgotten the login/passwords for computers/microscopes/server. What are they?
Fluorescent Microscopy Techniques FAQ
Which fluorophore probes can I visualize using Facility microscopes?
For the confocal microscopes, what laser wavelengths are available for excitation? Which fluorophores are appropriate?
Which confocal do I use (Zeiss Meta or Ultraview)? What are the differences?
What is the confocal z-resolution?
How do I prepare the slide (max coverslip thickness, anti-fade, sealant)? Storage?
How do I check for cross-talk or bleed-through of fluorescent dyes (i.e. controls)?
Can I do fluorescence recovery after photobleaching (FRAP) on Facility microscopes?
Can I do fluorescence resonance energy transfer (FRET) on Facility microscopes?
Electron Microscopy Techniques FAQ
What kinds of electron microscopy techniques are available?
Are immuno-electron microscopy services available?
How should I bring samples to the Facility for electron microscopy?
If I bring cells, how should they be delivered?
Can I bring formalin-fixed or paraffin-embedded samples for TEM?
If I don't need immuno-EM, how long does it take to prepare samples for viewing on the electron microscope?
Why does the sample size (tissue) have to be so small?
Immuno-electron Microscopy Prerequisites
Literature search: prior immuno-EM or immunofluorescence efforts with your tissue?
Quality of primary antibody.
Immunofluorescence tests of antibody under EM-like fixation conditions
Primer:
Three basic approaches to immuno-EM
-EMAIL microscopy_AT_jhmi.edu-
HOME
|
FAQ
|
SERVICES
|
JOIN US
|
MEMBERS
|
EQUIPMENT
|
RESOURCES