Difference between revisions of "Part:BBa K1489000:Experience"

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<I>Iowis Zhu</I>
 
<I>Iowis Zhu</I>
 
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Expression tests
 
BBa_K148900 was transformed into chemically competent DH5-alpha cells and plated overnight with chloramphenicol challenge. One colony was incubated in 5 mL LB media + 34 ug/mL chloramphenicol and grown to mid-log phase at 37oC. Arabinose was added to a final concentration of 0.2% to initiate protein production and cells were re-incubated at 37 oC for 21 hours. Cells were then pelleted and lysed with 10% SDS solution. Cell lysate was centrifuged at 13200 rpm in a tabletop centrifuge for 1 hour to separate soluble and insoluble fractions. Both fractions were loaded on an SDS-PAGE gel for western blot analysis using anti-His antibodies.
 
  
[[File:BovineGalectinExpression.jpg]]
 
 
Clear band of correct size can be seen in the soluble induced fraction, while no band is seen in the uninduced cells.
 
 
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Revision as of 20:22, 16 October 2014


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Please enter how you used this part and how it worked out.

Applications of BBa_K1489000

Expression tests BBa_K148900 was transformed into chemically competent DH5-alpha cells and plated overnight with chloramphenicol challenge. One colony was incubated in 5 mL LB media + 34 ug/mL chloramphenicol and grown to mid-log phase at 37oC. Arabinose was added to a final concentration of 0.2% to initiate protein production and cells were re-incubated at 37 oC for 21 hours. Cells were then pelleted and lysed with 10% SDS solution. Cell lysate was centrifuged at 13200 rpm in a tabletop centrifuge for 1 hour to separate soluble and insoluble fractions. Both fractions were loaded on an SDS-PAGE gel for western blot analysis using anti-His antibodies.

BovineGalectinExpression.jpg

Clear band of correct size can be seen in the soluble induced fraction, while no band is seen in the uninduced cells.

User Reviews

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