McClean:Blue Light Overview: Difference between revisions
No edit summary |
No edit summary |
||
| Line 7: | Line 7: | ||
==Setting Up an LED Array for Testing== | ==Setting Up an LED Array for Testing== | ||
If you need to test your constructs to see if they "work," this is best performed in batch on a roller drum. Arrange three LED's (460 nm emittance for | If you need to test your constructs to see if they "work," this is best performed in batch on a roller drum. Arrange three LED's (460 nm emittance for these constructs) at the 3, 9, and 12 o'clock positions of the roller drum so that they face the side of the drum (where they will be able to shine directly on culture tubes. Hook up the LED's as follows: | ||
[[Image:ledschem.png]] | [[Image:ledschem.png]] | ||
We use a 12V wall-wart with a 2.1 mm plug. | We use a 12V wall-wart with a 2.1 mm plug. | ||
Take an overnight culture of your cells, grown in SC -Leu-Trp-Ura, and use it to innoculate a 1:50 subculture in SC -Leu-Trp-Ura in a foil-wrapped tube as to exclude ambient light. Grow it at 30°C for 5 hours. Take this culture and aliquot about half of it into a new, clear culture tube. Place both sets of tubes on the outer lane of the roller drum at room temperature and turn the LEDs on. When sampling, take from 100 to 800 μL of culture and add it to an equal volume of cold PBS + 0.1% Tween and hold this solution at 4°C until ready to run at the FACS facility. | |||
==Modifying the LED Array to Vary Light Pulses== | |||
==Notes== | ==Notes== | ||
Revision as of 15:13, 7 October 2013
Overview
Working with blue light constructs (our CRY2 and CIB1- based induction system) requires working knowledge in yeast genetics and plasmid construction, simple electronics, and programming (in the Arduino environment.)
Plasmid & Strain Considerations
Generally, our CIB1 constructs are in plasmid backbones that are LEU2+, our CRY2 constructs are in those that are TRP1+, and our reporter constructs are in those that are URA3+. Thus, if following this convention, you must be using a strain that is prototrophic for these (i.e. LEU2, TRP1, and URA3 deficient.) We generally use either one of two strains for these purposes, yMM1146 or yMM1204. Most of our blue light plasmids are constructed with the pRS41(x) vectors (Sikorski and Hieter, 1989.) These are in our collection as pMM5-8. Note that these are the CEN/ARS (read: single copy) plasmids.
Setting Up an LED Array for Testing
If you need to test your constructs to see if they "work," this is best performed in batch on a roller drum. Arrange three LED's (460 nm emittance for these constructs) at the 3, 9, and 12 o'clock positions of the roller drum so that they face the side of the drum (where they will be able to shine directly on culture tubes. Hook up the LED's as follows:
We use a 12V wall-wart with a 2.1 mm plug.
Take an overnight culture of your cells, grown in SC -Leu-Trp-Ura, and use it to innoculate a 1:50 subculture in SC -Leu-Trp-Ura in a foil-wrapped tube as to exclude ambient light. Grow it at 30°C for 5 hours. Take this culture and aliquot about half of it into a new, clear culture tube. Place both sets of tubes on the outer lane of the roller drum at room temperature and turn the LEDs on. When sampling, take from 100 to 800 μL of culture and add it to an equal volume of cold PBS + 0.1% Tween and hold this solution at 4°C until ready to run at the FACS facility.
Modifying the LED Array to Vary Light Pulses
Notes
Please sign your name to your note by adding '''*~~~~''': to the beginning of your tip.
References
Gietz, R.D. and R.A. Woods. (2002) TRANSFORMATION OF YEAST BY THE Liac/SS CARRIER DNA/PEG METHOD. Methods in Enzymology 350: 87-96.
Contact
- Megan N McClean 14:01, 20 July 2011 (EDT)
or instead, discuss this protocol.
