Difference between revisions of "BBa K731700 and BBa K731710 measurements"
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In this page we are really proud to introduce you the protocol we (Giacomo and Anna) developed for the characterization transcriptional terminators effects on gene expression. (Tested on [[Part:BBa_K7|BBa_J64997]])
 
In this page we are really proud to introduce you the protocol we (Giacomo and Anna) developed for the characterization transcriptional terminators effects on gene expression. (Tested on [[Part:BBa_K7|BBa_J64997]])
  
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The develop of this protocolcost us not only sleepless night but also sunny and beautiful weekend of trekking so just shut up and read it all.
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The develop of this protocolcost us not only sleepless night but also sunny and beautiful weekend of trekking so take a hot cup of tea and read it all.
  
  
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'''
  
 
'''CELLS GROWTH AND SAMPLES PREPARATION (starting from a glycerol stock):'''
 
'''CELLS GROWTH AND SAMPLES PREPARATION (starting from a glycerol stock):'''
  
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* 100ul of cells in 10 ml fresh LB (4 glycerol stocks of each platform with or without terminator in BL21(DE3) pLysS) in 50ml falcon.
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* 100ul of cells (i.e. BL21(DE3) pLysS) tranformed with the measurement platform in 10 ml fresh Luria Bertani medium (LB)
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**NOTE:Antibiotic are at concentration of 0.1mg/ml ampicillin and 0.035mg/ml cloranphenicol
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NOTE1:Antibiotic are at concentration of 0.1mg/ml ampicillin and 0.035mg/ml cloranphenicol
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NOTE2:Four glycerol stocks of each platform with and without terminator will give you a good level of significance
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*grow 37°C in the termoshaker until OD ~ 0.4.
 
*grow 37°C in the termoshaker until OD ~ 0.4.
 
*(chill on ice for the whole duration of this point) dilute samples to OD 0.2 in order to have the same OD at the moment of induction.
 
*(chill on ice for the whole duration of this point) dilute samples to OD 0.2 in order to have the same OD at the moment of induction.

Revision as of 08:05, 21 September 2012

Hello world

In this page we are really proud to introduce you the protocol we (Giacomo and Anna) developed for the characterization transcriptional terminators effects on gene expression. (Tested on BBa_J64997)

The develop of this protocolcost us not only sleepless night but also sunny and beautiful weekend of trekking so take a hot cup of tea and read it all.


IN VIVO ANALYSIS


CELLS GROWTH AND SAMPLES PREPARATION (starting from a glycerol stock):

  • 100ul of cells (i.e. BL21(DE3) pLysS) tranformed with the measurement platform in 10 ml fresh Luria Bertani medium (LB)

NOTE1:Antibiotic are at concentration of 0.1mg/ml ampicillin and 0.035mg/ml cloranphenicol NOTE2:Four glycerol stocks of each platform with and without terminator will give you a good level of significance

  • grow 37°C in the termoshaker until OD ~ 0.4.
  • (chill on ice for the whole duration of this point) dilute samples to OD 0.2 in order to have the same OD at the moment of induction.
    • x = 10ml*0.2OD/0.4OD ___ where x are the ml of culture you need to take from the culture in the termoshaker.
    • LB = 10ml-x ____________ where LB are the ml of LB you need to add to x to obtain OD 0.2.
  • grow 37°C in the termoshaker until OD ~ 0.6.
  • induce with 0.5mM IPTG.
  • 3 hours induction at 37°C in the termoshaker.
  • chill falcon on ice
  • move 1ml of induced culture to an eppendorf.
  • sonication (3 repetition of 10s. 50% amplitude sonication and 30s. of pause).
  • 1.5min centrifuge.
  • move supernatant from eppendorf to cuvette.
  • add 2ml buffer (i.e.: PBS)
  • leave the cuvettes O/N in the 4°C fridge
  • fluorimetric measurements


Measurements of part K731700 and K731710