Difference between revisions of "Team:UCLA/Notebook/Honeybee Silk/17 May 2015"

(Growing Cultures)
 
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= May 17, 2015 =  
 
= May 17, 2015 =  
 
==Growing Cultures==
 
==Growing Cultures==
*Prepped 2 tubes of LB(5mL) with chloremphenicol and picked colonies of Bba-xxxx[http://benchling.com/dcancilla/f/mVVgFLnR-honeybee-silk-sequences/seq-cc4djRXz-promsilk-in-psb1c3/edit] to generate a starter culture for protein expression. Also prepped 2 tubes of of LB(5mL) with kanomycin and picked colonies of PET24a in order to miniprep and generate more plasmid.
+
*Prepped 2 tubes of LB(5mL) with chloremphenicol and picked colonies of Bba-xxxx[http://benchling.com/dcancilla/f/mVVgFLnR-honeybee-silk-sequences/seq-cc4djRXz-promsilk-in-psb1c3/edit] to generate a starter culture for protein expression. Also prepped 2 tubes of of LB(5mL) with kanamycin and picked colonies of PET24a in order to miniprep and generate more plasmid.
 
*We are growing the starter culture for the silk protein up to an OD of 0.8.  
 
*We are growing the starter culture for the silk protein up to an OD of 0.8.  
 
**For the starter culture, because we started the incubation at 3pm, and we dont want to overgrow, we will put the cells in the 30 C shaker until tomorrow morning, at which point we will transfer to the 37 degree shaker.
 
**For the starter culture, because we started the incubation at 3pm, and we dont want to overgrow, we will put the cells in the 30 C shaker until tomorrow morning, at which point we will transfer to the 37 degree shaker.
 
**The starter culture was placed in the 37 C incubator for one hour, and then transferred to the 30 C incubator at 4 PM
 
**The starter culture was placed in the 37 C incubator for one hour, and then transferred to the 30 C incubator at 4 PM

Latest revision as of 22:07, 15 July 2015

iGEM UCLA




May 17, 2015

Growing Cultures

  • Prepped 2 tubes of LB(5mL) with chloremphenicol and picked colonies of Bba-xxxx[http://benchling.com/dcancilla/f/mVVgFLnR-honeybee-silk-sequences/seq-cc4djRXz-promsilk-in-psb1c3/edit] to generate a starter culture for protein expression. Also prepped 2 tubes of of LB(5mL) with kanamycin and picked colonies of PET24a in order to miniprep and generate more plasmid.
  • We are growing the starter culture for the silk protein up to an OD of 0.8.
    • For the starter culture, because we started the incubation at 3pm, and we dont want to overgrow, we will put the cells in the 30 C shaker until tomorrow morning, at which point we will transfer to the 37 degree shaker.
    • The starter culture was placed in the 37 C incubator for one hour, and then transferred to the 30 C incubator at 4 PM