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Bold steps could potentially be done in the OT2
*are notes on the steps
the steps are followed by sub-steps which could/could not be automated
Get inserts
Prepare chemical competent DH10B-MOsp807II
Prepare MetClo Assembly vectors within the chemically competent DH10B-MOsp807II
miniprep vectors from picks chemical transformation vector in to cells
*must have different antibiotic selection market than insert plasmids
purify insert and metclo assembly vector plasmids
Conduct metclo assembly if insert and metclo assembly vector THIS IS MY DISSERTATION
*the protocol changes slightly for the size of the assembly
Purify and Analise Assembled DNA (insert in metclo assembly vector)
*if analysis is good move to step 7
Prepare a final assembly vector (with chemically compitent DH10B-MOsp807II) that will be accepting the plasmids from 5
*with a different antibiotic selection market to step 5 plasmids
*preparation as done in step 3
purify step 5 plasmids (another purification method different from step 6)
*the purification kit is different for p15a or F replication origin plasmids
repeat DNA assembly by metClo (step 5) with plasmids in step 7 and step 8
The text was updated successfully, but these errors were encountered:
PROTOCOL
in Zotero library
Bold steps could potentially be done in the OT2
*are notes on the steps
the steps are followed by sub-steps which could/could not be automated
miniprep vectors from picks
chemical transformation vector in to cells
*must have different antibiotic selection market than insert plasmids
*the protocol changes slightly for the size of the assembly
*if analysis is good move to step 7
*with a different antibiotic selection market to step 5 plasmids
*preparation as done in step 3
*the purification kit is different for p15a or F replication origin plasmids
The text was updated successfully, but these errors were encountered: