pf2-dta-rosa26 (Addgene inc)
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90
Structured Review
Addgene inc
pf2-dta-rosa26
Pf2 Dta Rosa26, supplied by Addgene inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/pf2-dta-rosa26/rosa26+locus/pmc03577784-48-68-78
Average 90 stars, based on 1 article reviews
Pf2 Dta Rosa26, supplied by Addgene inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/pf2-dta-rosa26/rosa26+locus/pmc03577784-48-68-78
Average 90 stars, based on 1 article reviews
pf2-dta-rosa26 - by Bioz Stars,
2026-10
90/100 stars
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Clone Assay:Article Title: A Novel Selection Marker for Efficient DNA Cloning and Recombineering in E. coli Article Snippet: Correct clones were identified by restriction enzyme digestion of miniprep DNA and confirmed by sequencing with Fab-BstE2-F and Fab-BssH2-R. pF-DTA was generated by recombineering with fragments from pDTA, which has the EF1a-DTA negative selection marker cloned into pBS backbone, cut by Apa LI deleting ampicillin resistance marker and pF by Afl III/ Dra III containing fabI . pF2-DTA was generated by cloning mfabI into pF-DTA by Fsp I/ Apa LI. pF2-DTA-Rosa26 was generated by inserting fragment from Sequencing:Article Title: A Novel Selection Marker for Efficient DNA Cloning and Recombineering in E. coli Article Snippet: Correct clones were identified by restriction enzyme digestion of miniprep DNA and confirmed by sequencing with Fab-BstE2-F and Fab-BssH2-R. pF-DTA was generated by recombineering with fragments from pDTA, which has the EF1a-DTA negative selection marker cloned into pBS backbone, cut by Apa LI deleting ampicillin resistance marker and pF by Afl III/ Dra III containing fabI . pF2-DTA was generated by cloning mfabI into pF-DTA by Fsp I/ Apa LI. pF2-DTA-Rosa26 was generated by inserting fragment from Generated:Article Title: A Novel Selection Marker for Efficient DNA Cloning and Recombineering in E. coli Article Snippet: Correct clones were identified by restriction enzyme digestion of miniprep DNA and confirmed by sequencing with Fab-BstE2-F and Fab-BssH2-R. pF-DTA was generated by recombineering with fragments from pDTA, which has the EF1a-DTA negative selection marker cloned into pBS backbone, cut by Apa LI deleting ampicillin resistance marker and pF by Afl III/ Dra III containing fabI . pF2-DTA was generated by cloning mfabI into pF-DTA by Fsp I/ Apa LI. pF2-DTA-Rosa26 was generated by inserting fragment from Selection:Article Title: A Novel Selection Marker for Efficient DNA Cloning and Recombineering in E. coli Article Snippet: Correct clones were identified by restriction enzyme digestion of miniprep DNA and confirmed by sequencing with Fab-BstE2-F and Fab-BssH2-R. pF-DTA was generated by recombineering with fragments from pDTA, which has the EF1a-DTA negative selection marker cloned into pBS backbone, cut by Apa LI deleting ampicillin resistance marker and pF by Afl III/ Dra III containing fabI . pF2-DTA was generated by cloning mfabI into pF-DTA by Fsp I/ Apa LI. pF2-DTA-Rosa26 was generated by inserting fragment from Marker:Article Title: A Novel Selection Marker for Efficient DNA Cloning and Recombineering in E. coli Article Snippet: Correct clones were identified by restriction enzyme digestion of miniprep DNA and confirmed by sequencing with Fab-BstE2-F and Fab-BssH2-R. pF-DTA was generated by recombineering with fragments from pDTA, which has the EF1a-DTA negative selection marker cloned into pBS backbone, cut by Apa LI deleting ampicillin resistance marker and pF by Afl III/ Dra III containing fabI . pF2-DTA was generated by cloning mfabI into pF-DTA by Fsp I/ Apa LI. pF2-DTA-Rosa26 was generated by inserting fragment from Cloning:Article Title: A Novel Selection Marker for Efficient DNA Cloning and Recombineering in E. coli Article Snippet: Correct clones were identified by restriction enzyme digestion of miniprep DNA and confirmed by sequencing with Fab-BstE2-F and Fab-BssH2-R. pF-DTA was generated by recombineering with fragments from pDTA, which has the EF1a-DTA negative selection marker cloned into pBS backbone, cut by Apa LI deleting ampicillin resistance marker and pF by Afl III/ Dra III containing fabI . pF2-DTA was generated by cloning mfabI into pF-DTA by Fsp I/ Apa LI. pF2-DTA-Rosa26 was generated by inserting fragment from Plasmid Preparation:Article Title: A Novel Selection Marker for Efficient DNA Cloning and Recombineering in E. coli Article Snippet: Correct clones were identified by restriction enzyme digestion of miniprep DNA and confirmed by sequencing with Fab-BstE2-F and Fab-BssH2-R. pF-DTA was generated by recombineering with fragments from pDTA, which has the EF1a-DTA negative selection marker cloned into pBS backbone, cut by Apa LI deleting ampicillin resistance marker and pF by Afl III/ Dra III containing fabI . pF2-DTA was generated by cloning mfabI into pF-DTA by Fsp I/ Apa LI. pF2-DTA-Rosa26 was generated by inserting fragment from |