pbluescript sk(−) phagemid vector (Agilent technologies)
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90
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Agilent technologies
pbluescript sk(−) phagemid vector
Pbluescript Sk(−) Phagemid Vector, supplied by Agilent technologies, 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/pbluescript+sk++phagemid+vector/pmc10758284-251-1-5
Average 90 stars, based on 1 article reviews
Pbluescript Sk(−) Phagemid Vector, supplied by Agilent technologies, 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/pbluescript+sk++phagemid+vector/pmc10758284-251-1-5
Average 90 stars, based on 1 article reviews
pbluescript sk(−) phagemid vector - by Bioz Stars,
2026-11
90/100 stars
Images
1) Product Images from "DNA cleavage assay for the identification of topoisomerase I inhibitors"
Article Title: DNA cleavage assay for the identification of topoisomerase I inhibitors
Journal: Nature protocols
doi: 10.1038/nprot.2008.174
Figure Legend Snippet:
Techniques Used:
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REAGENT or RESOURCE SOURCE IDENTIFIER Oligonucleotides gRNA targeting sequence for MRLC: UUACUGCUC AUCCUGUCCU this paper N/A Oligonucleotides for generating MRLC::SuperNova knockin flies, see Table S1 this paper N/A Primers for cloning MRLC, see Table S1 this paper N/A Primers for cloning the intracellular domain of Sdk, see Table S1 this paper N/A Primers for cloning GFP, see Table S1 this paper N/A Primers for cloning Ruby, see Table S1 this paper N/A Recombinant DNA pBFv-U6.2 National Institute of Genetics NIG: Software:Article Title: The Tricellular Junction Protein Sidekick Regulates Vertex Dynamics to Promote Bicellular Junction Extension. Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Oligonucleotides gRNA targeting sequence for MRLC: UUACUGCUC AUCCUGUCCU this paper N/A Oligonucleotides for generating MRLC::SuperNova knockin flies, see Table S1 this paper N/A Primers for cloning MRLC, see Table S1 this paper N/A Primers for cloning the intracellular domain of Sdk, see Table S1 this paper N/A Primers for cloning GFP, see Table S1 this paper N/A Primers for cloning Ruby, see Table S1 this paper N/A Recombinant DNA pBFv-U6.2 National Institute of Genetics NIG: |
