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Announcements

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Announcements Please pick up syllabus and index card from front desk. Fold the card lengthwise, write your name big and bold and use it as a name plate on your table. – PowerPoint PPT presentation

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Title: Announcements


1
Announcements
  • Please pick up syllabus and index card from front
    desk.
  • Fold the card lengthwise, write your name big and
    bold and use it as a name plate on your table.
  • Lecture notes will be available on Blackboard
    before class.
  • TBA this week continue working with your
    samples, practicing image collection and file
    management.
  • For viewing, sign up on confocal room door and
    with either me or Phil Oshel.

2
Agenda, Week 1
  • Introduction to Confocal Syllabus, etc.
  • Lab Fixation and staining of brine shrimp with
    fluorescent probes
  • Sytox Green for DNA
  • Rhodamine-phalloidin for microfilaments (enriched
    in muscle)
  • Unstained control for background fluorescence
  • Seminar from 4-5, Brooks 176 Heather Wiatrowski,
    Microbiology job candidate.
  • TBA this week and next complete staining, view
    results with Dr. Hertzler or Phil Oshel.

3
TBA Availability with Dr. HertzlerTwo 3-student
groups, 2 hours each
Time Tuesday Wednesday Thursday
8
9 SEM Cell Biology
10 Office
11 Hours
12
1
2
3 UCC
4 Faculty Meeting Seminar
4
Artemia Staining
  • Artemia at 1, 2, and 3 days (at 30oC) are
    available.
  • Fix with 3.7 formaldehyde in artificial seawater
    (ASW) for 1-2 hours.
  • After seminar
  • Wash 3 X 5 min with ASW.
  • Each group should label 3 tubes and stain
    overnight, covered with tin foil, with rocking
  • Sytox Green 15000 in ASW (gloves)
  • Rhodamine-phalloidin 140 in ASW (gloves)
  • nothing (control)
  • Tuesday, in Microscope suite (one locker
    available per group)
  • Wash 3 X 5 min with ASW.
  • Mount with either
  • 50 glycerol/50 ASW then 90 glycerol (store in
    fridg until TBA time), or
  • EtOH dehydration, 3X in 100 EtOH, then methyl
    salicylate (store at RT in dark)

5
Introduction to Confocal Imaging
  1. Confocal versus conventional fluorescence
  2. Optical sectioning
  3. Imaging modes and applications
  4. Advantages, limitations of confocal

6
Laser Scanning Confocal Microscope Components
Scan Head
Microscope
Controller box
Laser
Computer, display
7
Conventional versus confocal fluorescence
Conventional epifluorescence
Confocal epifluorescence
Sea urchin eggs (100 µm diameter) stained with
antibody to tubulin.
8
Widefield
Confocal
Sunflower pollen grain
Human brain slice
Rabbit muscle fibers
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