User:Daniel Goodman/Notebook/Cluzel/2010/02/24: Difference between revisions

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====Deposition Protocol====
====Deposition Protocol====
# place on glass slide: (try this first)
# place on glass slide: (try this first)
## dry cells for 1, 5, 10 min on cover slip, then transfer
## dry cells for 1, 5, 10 min in middle of glass slide
## 2 replicates per wait time
 
## 6 glass slides total
* 2 replicates per wait time
## cover top of agarose w/ cover slip to simulate similar pressure
* 6 glass slides total
* cover top of agarose w/ cover slip to simulate similar pressure in device
 
{|
|-
|min 0 ||  pour agarose
|-
|min 20 ||  remove agarose, place on square coverslips face up
|-
|min 21 ||  place cells on 6 slides
|-
|min 22 ||  place agarose & slip on G1.1, G1.2,
|-
|min 26 ||  place agarose & slip on G5.1, G5.2
|-
|min 31 ||  place agarose & slip on G10.1, G10.2
 


# place on agarose: (try this after if time allows)
# place on agarose: (try this after if time allows)

Revision as of 10:05, 24 February 2010


Cluzel Lab Notebook
Daniel Goodman
Main project page
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Redo glass experiment from 2/22

Prep

  • 3% w/v agarose
    • 5 ml LB, 150 mg agarose
    • heat in 80 deg. bath for 15 min
    • 108 ul per mold
  • 6 agarose block

Method

  1. Mold agarose into blocks
    1. Not using silicon molds, only testing bacterial dispersion on agarose/glass slide.
    2. waiting 20 min for agarose to dry in PDMS molds, at room temp; in future, will try different drying temps/dessication?
    3. cover agarose in mold with cover slip
  2. Place all 6 blocks on rectangular glass slides

Cells

  1. Grew up wild-type MG1655 E. coli to exponential phase, 0.1 ul of solution (measure OD)
  2. spot one 0.2 ul drops, on each agarose block/corresp. slide position, wait requisite time for each

Varying

  • wait time
    • 1 min, 5 min, 10 min

Deposition Protocol

  1. place on glass slide: (try this first)
    1. dry cells for 1, 5, 10 min in middle of glass slide
  • 2 replicates per wait time
  • 6 glass slides total
  • cover top of agarose w/ cover slip to simulate similar pressure in device
min 0 pour agarose
min 20 remove agarose, place on square coverslips face up
min 21 place cells on 6 slides
min 22 place agarose & slip on G1.1, G1.2,
min 26 place agarose & slip on G5.1, G5.2
min 31 place agarose & slip on G10.1, G10.2


  1. place on agarose: (try this after if time allows)
    1. after waiting 20 min for agarose to firm in mold, place on cover slip face up
    2. wait 0, 5, 10 min for agarose to dessicate
    3. apply cells to top surface of agarose
    4. gingerly move agarose to glass slide, face down


Measuring:

  • spot dispersion diameter

Data

dry time/surface 1 min 5 min 10 min
glass x x x
agarose x x x