Team:Stockholm/23 June 2010
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m (New page: {{Stockholm/Top2}} =Hassan= Started to use softwares for making 3D animations and/or movies, started by making protein A and IgG Protease. softwares used: #Molecular Maya #Chimera) |
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+ | =Andreas= | ||
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+ | ===Testing Top10 competent cells and antibiotic agar plates=== | ||
+ | |||
+ | ''Results from 22/6'' | ||
+ | |||
+ | {| border="1" cellspacing="0" cellpadding="2" | ||
+ | |'''Transformed plasmid''' | ||
+ | |'''Plate''' | ||
+ | |'''Growth''' | ||
+ | |- | ||
+ | |pEX | ||
+ | |100 ug/ml Amp | ||
+ | |Yes | ||
+ | |- | ||
+ | |None | ||
+ | |100 ug/ml Amp | ||
+ | |No | ||
+ | |- | ||
+ | |pEX | ||
+ | |25 ug/ml Cm | ||
+ | |No | ||
+ | |- | ||
+ | |None | ||
+ | |25 ug/ml Cm | ||
+ | |No | ||
+ | |} | ||
+ | |||
+ | Growth on Amp plate indicated transformation competence. No growth on other plates indicated good antibiotic selection. | ||
+ | |||
+ | '' '''Note:''' The transformed pEX vector was thought to carry a Cm resistance cassette insert. This was, however, discovered to be wrong.'' | ||
+ | |||
+ | ===Plasmid preparation of pEX vector=== | ||
+ | Two clones picked and each inoculated in 5 ml LB with Amp and grown ON in 37°C, 250 rpm. | ||
+ | |||
+ | ===Transformation with pMA vector=== | ||
+ | The pMA (BBa_K157000) vector could become useful for cloning and construction of our parts, as it carries the complete Freiburg prefix and suffix sequences (in contrast to the standard BioBrick vectors pSB1x3). | ||
+ | |||
+ | * Transformed Top10 cells with pMA vector carrying a Freiburg fusion His tag (BBa_K157011) insert. Cells plated on 100 ug/ml Amp plates. | ||
=Hassan= | =Hassan= | ||
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#Molecular Maya | #Molecular Maya | ||
#Chimera | #Chimera | ||
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+ | {{Stockholm/Footer}} |
Latest revision as of 10:31, 26 October 2010
Contents |
Andreas
Testing Top10 competent cells and antibiotic agar plates
Results from 22/6
Transformed plasmid | Plate | Growth |
pEX | 100 ug/ml Amp | Yes |
None | 100 ug/ml Amp | No |
pEX | 25 ug/ml Cm | No |
None | 25 ug/ml Cm | No |
Growth on Amp plate indicated transformation competence. No growth on other plates indicated good antibiotic selection.
Note: The transformed pEX vector was thought to carry a Cm resistance cassette insert. This was, however, discovered to be wrong.
Plasmid preparation of pEX vector
Two clones picked and each inoculated in 5 ml LB with Amp and grown ON in 37°C, 250 rpm.
Transformation with pMA vector
The pMA (BBa_K157000) vector could become useful for cloning and construction of our parts, as it carries the complete Freiburg prefix and suffix sequences (in contrast to the standard BioBrick vectors pSB1x3).
- Transformed Top10 cells with pMA vector carrying a Freiburg fusion His tag (BBa_K157011) insert. Cells plated on 100 ug/ml Amp plates.
Hassan
Started to use softwares for making 3D animations and/or movies, started by making protein A and IgG Protease.
softwares used:
- Molecular Maya
- Chimera