Friday 07/19/13

9:50 A – 5:30 P

Banff

  • finish draft schedule
  • upload draft schedule to website
  • finish activities sheet
  • send participant email list, activities sheet, draft schedule, and notes about filming talks and requesting titles to Andrew.

Planning with Jeff for next week

Experiments on deck

  • Setup next week to deep sequence library
  • troubleshoot exon selection next week
  • RNA seq cells

troubleshooting RNA isolation

  • substantial nucleotide fraction left even after ethanol precipitation. Better to compare levels by gel than by nano-drop.

Probe making

  • finish in vitro transcription reactions, check on gel
  • ran 1uL of 20 uM cy5 labeled primer next to ladder.
  • very poor incorporation: very strong cy5 band below the RNA bands.
    cy5_RNA
  • cy5 labeled primer runs faster than unlabeled cy5.
  • usual 2% ultrapure agarose gel run for 10 min in sodium borax with Ultra low range ladder on left, bright ladder band is 50bp.

STORM

  • Finish O/N run of slide 1 round 2, Bxc. Transfer data
  • O/N STORM analysis of Gdc data still running

Chromatin

  • probe BLAST ran O/N with original 25mer oligo list, not pruned primer converted list.
  • rerunning.
  • fixing bugs, converting to functions, making sure results against separate genomes are documented in separate fasta files.

To Do

  • Pc Psc analysis!
  • Review!
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