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three months ago i (we) started a project- recombination of the lux operon (which glows in the dark) into E. coli. ergo, making a non glowing bacteria into a glowing bacteria! last week we finished up this project. three months of protocols and gels and DNAses... boiled down to a bunch of bacteria that did not glow for me. :'( even the "sure shot" plasmid to plasmid transformation did not work for me. uhhhhg. maybe sounds like gobbledy gook to you. but to me this is total </3 . i've been all emo this week. i feel like science hates me. oh. oh. and also, i've been growing mouse cancer cells (P3 cells) in a flask for tissue culture. it's also been alive for 3 months with no contamination! until, the very last day before i threw it away (and ironically the same day of my lux disappointment). contamination. evil fungus. eeeeeevil. contaminating my kids! keratin project has not been going well either but that's a whole other story... and all my professor says to me is "SUCH IS SCIENCE."
sigh. ok. i'm over it already. need to stop thinking about science. ok, how about this-
MY CALENDAAAAARS HAVE ARRIVED!
LISTENING TO: CARPE DIEM by Todor and Emily Haines
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oh who am i kidding. i am still emo about this.
maybe i didn't use enough ligase? i don't understand. where did the keratin go wrong? and the controls worked so i know the pGEM plasmid was good, the ampicilin was good, the xgal was good, the CIP was good. only the two lux experiments didn't work. whyyyyyyyyyyyy? i really can't get over this. WHYYYYYYY? WEISHEME????? POURQUOI????? AHHHRG!
LISTENING TO: PAPER FLOAT by Cassettes Won't Listen
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Elli's Darkroom - Polaroids - [link]
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je ne suis pas la fou,je suis l'avion!
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ToMzorz .. design_develop_create
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