BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//Hooker Imaging Core - ECPv6.15.14//NONSGML v1.0//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
X-ORIGINAL-URL:https://www.med.unc.edu/hic-imaging
X-WR-CALDESC:Events for Hooker Imaging Core
REFRESH-INTERVAL;VALUE=DURATION:PT1H
X-Robots-Tag:noindex
X-PUBLISHED-TTL:PT1H
BEGIN:VTIMEZONE
TZID:America/New_York
BEGIN:DAYLIGHT
TZOFFSETFROM:-0500
TZOFFSETTO:-0400
TZNAME:EDT
DTSTART:20240310T070000
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:-0400
TZOFFSETTO:-0500
TZNAME:EST
DTSTART:20241103T060000
END:STANDARD
BEGIN:DAYLIGHT
TZOFFSETFROM:-0500
TZOFFSETTO:-0400
TZNAME:EDT
DTSTART:20250309T070000
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:-0400
TZOFFSETTO:-0500
TZNAME:EST
DTSTART:20251102T060000
END:STANDARD
BEGIN:DAYLIGHT
TZOFFSETFROM:-0500
TZOFFSETTO:-0400
TZNAME:EDT
DTSTART:20260308T070000
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:-0400
TZOFFSETTO:-0500
TZNAME:EST
DTSTART:20261101T060000
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20251103T080000
DTEND;TZID=America/New_York:20251107T170000
DTSTAMP:20260404T171904
CREATED:20251001T185528Z
LAST-MODIFIED:20251029T211603Z
UID:10000394-1762156800-1762534800@www.med.unc.edu
SUMMARY:Workshop--Single Molecule Localization Microscopy and TIRF
DESCRIPTION:Test out the Abbelight SMLM and TIRF system\nTaylor Hall 229\nCo-hosted by Jenn Marks with Evident Scientific (formerly Olympus). \nSee the system working with one of the demo slides or test your own sample. \nSign up for a time slot with the 👉 Doodle Sign-Up Sheet \nFor maximal success with your samples\, contact Paul Barthélémy as soon as possible to ensure you have the optimal sample holders and fluorophores (pdf). We have a small amount of secondary antibodies with appropriate fluorophores available on-site for sample preparation prior to your imaging session. \nWatch the UNC Sample Prep Webinar from Oct. 9\, 2025. \nPractical notes:\n1: SMLM will not work with your standard confocal sample of a coverslip mounted on a slide with mounting media using whichever fluorophores you have in your freezer. The preparation is very similar to your confocal protocol\, but there are a few extremely critical details that might differ. You will likely need to generate a specific sample for the demo.\n2: Fluorophores needed for SMLM also work great for standard fluorescence applications\, so anything you might need to buy for a successful demo can likely be used for other applications. \nPDF product brochure
URL:https://www.med.unc.edu/hic-imaging/event/workshop-single-molecule-localization-microscopy-and-tirf/
END:VEVENT
END:VCALENDAR