Difference between revisions of "20.109(F16): TA notes for M1"

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(M1D2)
(M1D3)
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===M1D3===
 
===M1D3===
Per group, aliquot:
+
In incubator, have (per group)
*1% LMP agarose
+
*TK6 cells at 500,000 cells/mL (10 mL)
*H2O2 and MMS
+
 
*Alkyline lysis solution
+
On front bench, prepare (per group)
*Alkyline electrophoresis buffer
+
*bottomless 96-well plates (3)
*Neutralization buffer
+
*glass slides (2)
*SYBR Gold buffer
+
*binder clips (8)
 +
*water bath at 43 °C with
 +
*1% LMP agarose (3 mL)
 +
*lysis buffer stock (40 mL)
 +
*Triton X-100 (400 μL)
 +
*Neutralization buffer (50 mL)
 +
*SYBR Gold buffer (20 mL)
 +
 
 +
In cold room, prepare (per group)
 +
*electrophoresis gel boxes with double-sided tape (2 teams or 4 CometChips per box)
 +
*alkyline electrophoresis buffer (500 mL)
  
 
===M1D4===
 
===M1D4===

Revision as of 20:28, 20 September 2016

20.109(F16): Laboratory Fundamentals of Biological Engineering

Engelward PNAS 2006.png

Schedule Fall 2016        Announcements        Assignments        Homework        Communication
       1. Measuring Genomic Instability        2. Manipulating Metabolism        3. Engineering Biomaterials              

M1D1

Per group, aliquot

  • 50 mL 1x PBS
  • in TC room, 15 mL of “TK6 media”

M1D2

Per group, aliquot

  • in main lab
    • 10 mL 1x PBS
    • 2 eppendorf tubes of 0.3% LMP agarose (in eppendorf water bath)
    • large scheme of the plate so they can keep track of how to load chips
  • and separately, in the TC hood,
    • 10 mL 1x PBS
    • 25 mL TK6 media
    • 2 eppendorf tubes of 0.3% LMP agarose (in water bath at 43 °C)
    • 2x 15 mL of TK6 cells at 500,000 cells/mL

Set up hoods in TC room with, per group:

  • 4 binder clips
  • 1 glass slide
  • 1 bottomless 96-well plate
  • 1 razor blade
  • Pasteur pipets
  • sharp jar
  • pipet aid
  • pen
  • team sticker to identify glass slides
  • printout of today's protocol
  • large scheme of the plate to hang in TC so they can keep track of how to load chips

M1D3

In incubator, have (per group)

  • TK6 cells at 500,000 cells/mL (10 mL)

On front bench, prepare (per group)

  • bottomless 96-well plates (3)
  • glass slides (2)
  • binder clips (8)
  • water bath at 43 °C with
  • 1% LMP agarose (3 mL)
  • lysis buffer stock (40 mL)
  • Triton X-100 (400 μL)
  • Neutralization buffer (50 mL)
  • SYBR Gold buffer (20 mL)

In cold room, prepare (per group)

  • electrophoresis gel boxes with double-sided tape (2 teams or 4 CometChips per box)
  • alkyline electrophoresis buffer (500 mL)

M1D4

Per group, aliquot:

  • 15 mL 1x PBS
  • H2O2
  • Alkyline lysis solution
  • Warm M059J/K culture medium

M1D5

Per group, aliquot in TC room:

  • 5 mL of 0.1% gelatin
  • 10 mL of PBS
  • 3 mL of 1X trypsin
  • 15 mL of M059J/K media
  • M059J/K in T25 flasks

M1D6

Per group, aliquot in TC room:

  • 10 mL of 1x TBS
  • 500 uL of 10% BSA, frozen stock in -20C
  • Triton X-100 at front bench
  • Primary antibodies

M1D7

Per group, aliquot

  • 5 mL of 1x TBS