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Tag Archives: STORM
Tuesday 12/11/12
10:10 A Check PCRs (in blocks 3A (sim screening) and 3B (Espl screening) better way to do this: complementation test back to original sim[D] and Espl[D] lines. Just need to expand those lines back to bottles, will need ~100 vials … Continue reading
Monday 12/10/12
9:50 A -7:40P, 8:40P – 12:30 A yari lab meeting De-noising: use conventional image as low pass filter to remove non-blinking background Use conventional alignment for drift correction, translate all STORM movies to match multi-color conventional image. Use field of … Continue reading
Sunday 12/09/12
10:20 A – 7:30P, 9:30-11:00P STORM 750 1600 mA = 18 mW 1.45 mW 405 200 mW set 647 Made new Glox 750 not switching well. Not sure if it’s just low labeling (405 looked okay but not strong). 647 … Continue reading
Posted in Summaries
Tagged analysis, cell labeling, coding, section staining, STORM, STORM2
Comments Off on Sunday 12/09/12
Monday 12/03/12
8:45 A — 7:30 P, 8:45P – 12:40 A Confocal data Finish O/N confocal run transfer files modify imviewer LSM to automatically detect all .lsm files in a folder and convert them all to TIF / labeled stacks of TIFs … Continue reading
Saturday, 11/24/12
11:15 A -7:30P, 9:30P – 11:45 P UltraCryo coverslip DFISH Hot washes for DFISH coverslips RT wash check sections on coverglass A. Be very careful to keep sections covered with buffer. Staining definetely works. Signal somewhat dimer than expected, but … Continue reading
STORM2 11/24/12
Laser powers 405: 1.5 mW 488: 115 mW at 45% power 561: 135 mW at 200 mW GUI/laserhead 642: 135 mW at 200 mW GUI/laserhead 750: 250mW at 1800 mA. –> too high? 750: 120 mW at 1400 mA –> … Continue reading
Sunday 11/18/12
10:15 A – 6:50 P, 7:50P – 10:30P Probe making have not confirmed nicking enzyme concentration for digestion. Canceled PAGE introduction with Bryan, will attempt again later. Telomeres Read over telomere manuscript from John Wu Imaging telomeres: 656 = 60 … Continue reading
Thursday 11/07/12
9:30 A -8:00P, 9:30-11:00P check STORM. — run finished without losing focus. Summary of inv run: Unfortunately 514 doesn’t work either as a double label. inv-Epc male a lot of promising double spots, but it’s a litter harder to sort … Continue reading
Wednesday 11/06/12
9:45 A – 8:30 P write to ML about bistability write to Bender about Hox model. — apparently email contact is not recommended. Try phone tomorrow. write summary of Francis suggestions remove medium from S2 cells, add fresh medium. Reduce … Continue reading
Tuesday 11/06/12
9:15 A – 9:00P, 10:ooP-11:00P (vote, 8:45A) Washing out probe from on slide DFISH. hot wash at 60C -forgot for 2hrs (oops!) stain with Hoechst and WGA-488 Working on presentation for Francis group meeting STORM characterizing embryo background (see images) … Continue reading