User:NYOUSHA Yousefi/Notebook/Protein Engineering/2013/01/22

From OpenWetWare

(Difference between revisions)
Jump to: navigation, search
(Objective 2)
(Procedure 2)
Line 24: Line 24:
==Procedure 2==  
==Procedure 2==  
 +
# The tube of the sample was placed in liquid nitrogen for 15 min to completely freeze them
 +
# When all the liquid of the sample was solidified, the samples were place under vacuum to make the ice to sublimate into vapor water directly
 +
# The vacuum was allowed to run over night for 24h   
<!-- ##### DO NOT edit below this line unless you know what you are doing. ##### -->
<!-- ##### DO NOT edit below this line unless you know what you are doing. ##### -->
|}
|}
__NOTOC__
__NOTOC__

Revision as of 09:27, 29 January 2013

Project name Main project page
Previous entry      Next entry

Entry title

Culturing antibiotic resistant bacteria producing myoglobin and hemoglobin

Objective 1

Ampicillin and Kenamycin were the antibiotics used for culturing

Procedure 1

  1. 5ml of LB medium was added to two set of sterile tubes by 10 ml pipets
  2. 5ul of Ampicillin was added to one tube and Kenamycin was added to the other tube
  3. The frozen cells in glycerol were taken out of the -80 degree C fridge
  4. Bacteria expressing Myoglobin were added to the media tube containing Ampicillin because it has Ampicillin resistance
  5. PQE-80 bacteria were added to media tube containing Kenamycin becasue it has Kenamycin resistance
  6. The tubes were places in the incubator/shaker at 37 degree C for 24h

Objective 2

Lyophilization of 0.0058g Myoglobin, 20ml PH 7 phosphate, 0.4961 mg KCL sample

Procedure 2

  1. The tube of the sample was placed in liquid nitrogen for 15 min to completely freeze them
  2. When all the liquid of the sample was solidified, the samples were place under vacuum to make the ice to sublimate into vapor water directly
  3. The vacuum was allowed to run over night for 24h


Personal tools