IGEM:Harvard/2006/DNA nanostructures/Notebook/2006-7-13

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Initial Container v3.2 Preparation and Analysis

  • Oligos arrived this morning from Invitrogen. Plan for today is to mix oligos together into pre-stocks, and then working stocks, and then try some initial folding experiments and gel analysis.

Creating pre-working stocks and working stocks from design 3.2 oligos

  • Mix 10 μL of each 50 μM stock oligo
oligo desc plate location total
c3.2.1 core barrel 3.2p1A01–3.2p1H10 94
c3.2.2 core top lid 3.2p2A01–3.2p2C04 28
c3.2.3 core bottom lid 3.2p2C05–3.2p2E10 30
c3.2.4 barrel at inside apatamer locations -aptamers 3.2p2E11–3.2p2F01 3
c3.2.5 barrel at outside aptamer locations -aptamers 3.2p2F02–3.2p2F04 3
c3.2.6 barrel at inside apatamer locations +aptamers 3.2p2F05–3.2p2F07 3
c3.2.7 barrel at outside aptamer locations +aptamers 3.2p2F08–3.2p2F10 3
c3.2.8 barrel at latch locations -latches 3.2p2F11–3.2p2F12 2
c3.2.9 lid at latch locations -latches (empty) 0
c3.2.10 barrel at latch locations +latch1 +latch2 3.2p2G01–3.2p2G02 2
c3.2.11 latch from barrel +latch1 -latch2 3.2p2G03–3.2p2G04 2
c3.2.12 latch from barrel -latch1 +latch2 3.2p2G05–3.2p2G06 2
c3.2.13 lid at latch locations +latch1 +latch2 (empty) 0
c3.2.14 latch from lids +latch1 -latch2 3.2p2G07–3.2p2G08 2
c3.2.15 latch from lids -latch1 +latch2 3.2p2G09–3.2p2G10 2
c3.2.16 latch staples +latch2 3.2p2G11–3.2p2H02 4
c3.2.17 displacement strands latch1 3.2p2H03–3.2p2H06 4
c3.2.18 displacement strands latch2 3.2p2H07–3.2p2H10 4


Make c3.2 Working stocks

c3.2 Folding Experiment

Gel analysis