http://www.wormbook.org/db/misc/search.cgi?search_html=on;search_preprints=on;query=bleach WebApr 21, 2024 · Timing: 15 min. 10% (w/v) agarose pad is used to immobilize worms for live-cell imaging. High quality agarose pad with stable humidity is the key step for live-cell imaging of C. elegans. Prepare 10% (w/v) agarose solution: Boil 2 g agarose in 20 mL M9 buffer in a 50 mL Erlenmeyer flask.
Population scale nucleic acid delivery to Caenorhabditis …
http://www.wormbook.org/chapters/www_strainmaintain/strainmaintain.html Webwhen bleach synchronization is used, population growth is dependent on starting census size and, therefore, effects subsequent growth and population numbers. In addition, C. elegans strains vary in their cuticle sensitivity, exposure time, and stress response to bleach synchronization making it difficult to assay many strains at a time5,6,7,8,9. chris koultukis
Vis. Exp. Caenorhabditis elegans Populations - Andersen Lab
WebOct 22, 2013 · The EIW assay involves bleaching staged, gravid adult C. elegans to remove the cuticle and separate the retained eggs from the animal. Prior to bleaching, worms are exposed to bacteria (or any type of environmental cue) for a fixed period of time. ... and 12.5 ml KPO 4 buffer (54.15 g KH 2 PO 4 and 17.8 g K 2 HPO 4 in 500 ml of dH … WebMay 4, 2024 · The C. elegans embryo is also an interesting model system to study biological processes at a very early stage, e.g., the formation of functional neuronal … WebStaining protocol for C. Elegans embryos. Wash several plates of worms off with M9. Use microfuge tubes to spin worms. Wash 2X with 1ml M9 buffer. Pool worms into 1 or 2 microfuge tubes. Use the tubes that have siliconized to prevent loss of embryos. Add 1 ml of Bleach solution (1ml 10 N NaOH 8ml H20) to worm pellet. chris kounelis