ecori-cut pbluescript sk+ vector (Agilent technologies)
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ecori-cut pbluescript sk+ vector
Ecori Cut Pbluescript Sk+ 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/ecori-cut+pbluescript+sk++vector/us06911309-318-20-24
Average 90 stars, based on 1 article reviews
Ecori Cut Pbluescript Sk+ 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/ecori-cut+pbluescript+sk++vector/us06911309-318-20-24
Average 90 stars, based on 1 article reviews
ecori-cut pbluescript sk+ vector - by Bioz Stars,
2026-09
90/100 stars
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Polymerase Chain Reaction:Article Title: Nucleic acids encoding MTAse Article Snippet: .. The PCR amplification product was double digested with restriction enzymes EcoRI/BamHI, separated on a 0.8% agarose gel in 1×TA buffer, recovered from the gel using “GENE CLEAN”™ Kit (Bio101), subcloned into Article Title: Nucleic acids encoding MTAse Article Snippet: .. The PCR product was digested with restriction enzymes EcoRI/Pst I, purified electrophoretically on a 0.8% agarose gel and subcloned into Amplification:Article Title: Nucleic acids encoding MTAse Article Snippet: .. The PCR amplification product was double digested with restriction enzymes EcoRI/BamHI, separated on a 0.8% agarose gel in 1×TA buffer, recovered from the gel using “GENE CLEAN”™ Kit (Bio101), subcloned into Agarose Gel Electrophoresis:Article Title: Nucleic acids encoding MTAse Article Snippet: .. The PCR amplification product was double digested with restriction enzymes EcoRI/BamHI, separated on a 0.8% agarose gel in 1×TA buffer, recovered from the gel using “GENE CLEAN”™ Kit (Bio101), subcloned into Article Title: Nucleic acids encoding MTAse Article Snippet: .. The PCR product was digested with restriction enzymes EcoRI/Pst I, purified electrophoretically on a 0.8% agarose gel and subcloned into Plasmid Preparation:Article Title: Nucleic acids encoding MTAse Article Snippet: .. The PCR amplification product was double digested with restriction enzymes EcoRI/BamHI, separated on a 0.8% agarose gel in 1×TA buffer, recovered from the gel using “GENE CLEAN”™ Kit (Bio101), subcloned into Article Title: Nucleic acids encoding MTAse Article Snippet: .. The PCR product was digested with restriction enzymes EcoRI/Pst I, purified electrophoretically on a 0.8% agarose gel and subcloned into Article Title: Nucleic acids encoding MTAse Article Snippet: .. The Not I/HindII-DNA fragment from subclone MTAP-4 and the large HindII/EcoRI fragment from subclone MTAP-2 were mixed and subcloned into Not Sequencing:Article Title: Nucleic acids encoding MTAse Article Snippet: .. The PCR amplification product was double digested with restriction enzymes EcoRI/BamHI, separated on a 0.8% agarose gel in 1×TA buffer, recovered from the gel using “GENE CLEAN”™ Kit (Bio101), subcloned into DNA Sequencing:Article Title: Nucleic acids encoding MTAse Article Snippet: .. The PCR amplification product was double digested with restriction enzymes EcoRI/BamHI, separated on a 0.8% agarose gel in 1×TA buffer, recovered from the gel using “GENE CLEAN”™ Kit (Bio101), subcloned into Purification:Article Title: Nucleic acids encoding MTAse Article Snippet: .. The PCR product was digested with restriction enzymes EcoRI/Pst I, purified electrophoretically on a 0.8% agarose gel and subcloned into other:Article Title: Nucleic acids encoding MTAse Article Snippet: Two EcoRI insert fragments (850 bp and 1100 bp) from the representative phage clone, designated as MTAp-1, were subcloned into Article Title: Characterization of Maize Cytochrome P450 Monooxygenases Induced
in Response to Safeners and Bacterial
Pathogens Article Snippet: For cloning, one-half of the RT-PCR products derived from a single amplification reaction were |